1,3-Bis(4-chloro­phen­yl)-1-methyl-1H-benzo[f]chromene

Chen, R.; Zhou, Q.

doi:10.1107/S1600536810022610

1,3-Bis(4-chlorophenyl)-1-methyl-1H-benzo[f]chromene

The title compound, C₂₆H₁₈Cl₂O, is a heterocyclic structure consisting of a benzo[f]chromene ring and two aromatic rings. The non-H atoms of the benzo[f]chromene ring are almost coplanar (rms deviation = 0.107 Å), and the methyl C atom lies 1.340 (4) Å from the mean plane of the benzo[f]chromene ring. The chromene ring forms dihedral angles of 88.45 (2)° with the benzene ring linked to the quaternary C atom and 50.74 (3)° with the benzene ring linked to the 3-position, while the dihedral angle between the two benzene rings is 67.58 (3)°.

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Supporting information

	Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536810022610/zq2041sup1.cif Contains datablocks global, I
	Structure factor file (CIF format) https://doi.org/10.1107/S1600536810022610/zq2041Isup2.hkl Contains datablock I

CCDC reference: 786678

checkCIF report

Key indicators

Single-crystal X-ray study
T = 296 K
Mean (C-C) = 0.003 Å
R factor = 0.042
wR factor = 0.095
Data-to-parameter ratio = 17.4

checkCIF/PLATON results

No syntax errors found



Alert level C
PLAT910_ALERT_3_C Missing # of FCF Reflections Below Th(Min) .....          6
PLAT911_ALERT_3_C Missing # FCF Refl Between THmin & STh/L=  0.600          7
PLAT912_ALERT_4_C Missing # of FCF Reflections Above STh/L=  0.600         37

Alert level G
PLAT793_ALERT_4_G The Model has Chirality at C1      (Verify) ....          R

   0 ALERT level A = In general: serious problem
   0 ALERT level B = Potentially serious problem
   3 ALERT level C = Check and explain
   1 ALERT level G = General alerts; check

   0 ALERT type 1 CIF construction/syntax error, inconsistent or missing data
   0 ALERT type 2 Indicator that the structure model may be wrong or deficient
   2 ALERT type 3 Indicator that the structure quality may be low
   2 ALERT type 4 Improvement, methodology, query or suggestion
   0 ALERT type 5 Informative message, check

Comment top

Chromenes (2H- and 4H-chromenes) constitute an important class of scaffolds found in many naturally occurring and synthetic molecules showing unique biological and pharmacological activities including spasmolytic, diuretic, anticoagulant, anticancer activities and so on. In this article, the crystal structure of the title compoud 1,3-di(4-chloro-phenyl)-1-methyl-1H-benzo[f]chromene was determined (Fig. 1–2). Its main structure unit consists of a benzo[f]chromene ring and two aromatic rings, in which the non-H atoms of the benzo[f]chromene ring are almost coplanar, and the methyl atom C26 lies 1.340 (4) Å from the benzo[f]chromene ring. The chromene ring forms dihedral angles of 88.45 (2)° with the benzene ring linked to the quaternary carbon atom C1, and 50.74 (3)° with the other benzene ring linked to C12, while the dihedral angle between the two benzene rings is 67.58 (3)°.

Related literature top

For the construction of a 4H-chromene scaffold, see: Shi & Shi (2007); Zeni & Larrock (2004). For the biological and pharmacological activity of 4H-chromene derivatives, see: Kidwai et al. (2005). For 4H-chromene derivatives possessing a tertiary carbon in the scaffold, see: Liu et al. (2010); Wang & Zhu (2010). For iron trichloride-catalysed synthesis of 4H-chromenes, see: Kozlikovskii et al. (1986).

Experimental top

The title compound was synthesized by treating (E)-1,3-bis(4-chlorophenyl)but-2-en-1-one (0.291 g,1 mmol) with 2-naphthol (0.144 g,1 mmol) in the presence of ferric trichloride (0.16 g, 1.0 mmol) as a catalyst in 1,2-dichloroethane (3 ml) under stirring at reflux for 6 h. Upon completion, the resulting mixture was diluted with dichloromethane (10 ml) and filtered through Celite. After evaporation of the solvent under vacuum, the residue was purified by column chromatography on silica gel (200–300 mesh) using Petroleum ether-EtOAc (30:1) as eluent to give the title compound (0.19 g, 40%). Suitable crystals of the title compound were obtained by slow evaporation of ethanol solution at room temperature.

Computing details top

Data collection: PROCESS-AUTO (Rigaku, 1998); cell refinement: PROCESS-AUTO (Rigaku, 1998); data reduction: CrystalStructure (Rigaku/MSC, 2004); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 for Windows (Farrugia, 1997); software used to prepare material for publication: CrystalStructure (Rigaku/MSC, 2004).

Figures top

	Fig. 1. The molecular structure of the title compound, with the atomic labeling scheme. Displacement ellipsoids are drawn at the 50% probability level.
	Fig. 2. The packing of the crystal structure of the title compound. The C, O and Cl atoms are grey, red and brown, respectively.

1,3-Bis(4-chlorophenyl)-1-methyl-1H-benzo[f]chromene top

Crystal data top

C₂₆H₁₈Cl₂O	Z = 2
M_r = 417.33	F(000) = 432.00
Triclinic, P1	D_x = 1.368 Mg m⁻³
Hall symbol: -P 1	Mo Kα radiation, λ = 0.71075 Å
a = 8.9554 (6) Å	Cell parameters from 6736 reflections
b = 9.4439 (6) Å	θ = 3.0–27.4°
c = 12.3206 (7) Å	µ = 0.34 mm⁻¹
α = 93.511 (2)°	T = 296 K
β = 102.0453 (15)°	Chunk, colorless
γ = 94.287 (2)°	0.42 × 0.37 × 0.28 mm
V = 1013.05 (11) Å³

Data collection top

Rigaku R-AXIS RAPID diffractometer	2783 reflections with F² > 2σ(F²)
Detector resolution: 10.00 pixels mm^-1	R_int = 0.021
ω scans	θ_max = 27.5°
Absorption correction: multi-scan (ABSCOR; Higashi, 1995)	h = −11→11
T_min = 0.874, T_max = 0.910	k = −12→12
10050 measured reflections	l = −15→14
4596 independent reflections

Refinement top

Refinement on F²	w = 1/[σ²(F_o²) + (0.001P)² + 0.920P] where P = (F_o² + 2F_c²)/3
R[F² > 2σ(F²)] = 0.042	(Δ/σ)_max < 0.001
wR(F²) = 0.095	Δρ_max = 0.28 e Å⁻³
S = 1.00	Δρ_min = −0.33 e Å⁻³
4596 reflections	Extinction correction: SHELXL97 (Sheldrick, 2008)
264 parameters	Extinction coefficient: 0.0188 (6)
H-atom parameters constrained

Crystal data top

C₂₆H₁₈Cl₂O	γ = 94.287 (2)°
M_r = 417.33	V = 1013.05 (11) Å³
Triclinic, P1	Z = 2
a = 8.9554 (6) Å	Mo Kα radiation
b = 9.4439 (6) Å	µ = 0.34 mm⁻¹
c = 12.3206 (7) Å	T = 296 K
α = 93.511 (2)°	0.42 × 0.37 × 0.28 mm
β = 102.0453 (15)°

Data collection top

Rigaku R-AXIS RAPID diffractometer	4596 independent reflections
Absorption correction: multi-scan (ABSCOR; Higashi, 1995)	2783 reflections with F² > 2σ(F²)
T_min = 0.874, T_max = 0.910	R_int = 0.021
10050 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.042	264 parameters
wR(F²) = 0.095	H-atom parameters constrained
S = 1.00	Δρ_max = 0.28 e Å⁻³
4596 reflections	Δρ_min = −0.33 e Å⁻³

Special details top

Refinement. Refinement using reflections with F² > 2.0 σ(F²). The weighted R-factor(wR), goodness of fit (S) and R-factor (gt) are based on F, with F set to zero for negative F. The threshold expression of F² > 2.0 σ(F²) is used only for calculating R-factor (gt).

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å²) top

	x	y	z	U_iso*/U_eq
Cl1	0.25919 (11)	−0.05748 (9)	0.82025 (6)	0.0899 (3)
Cl2	0.54898 (11)	0.29006 (9)	−0.01095 (6)	0.0875 (2)
O1	0.27277 (19)	0.50754 (14)	0.53308 (12)	0.0492 (4)
C1	0.1329 (2)	0.4692 (2)	0.29332 (18)	0.0405 (5)
C2	0.2049 (2)	0.6121 (2)	0.35548 (17)	0.0380 (4)
C3	0.2145 (2)	0.7416 (2)	0.29947 (18)	0.0406 (5)
C4	0.1688 (2)	0.7468 (2)	0.1828 (2)	0.0521 (6)
C5	0.1790 (3)	0.8718 (2)	0.1324 (2)	0.0614 (7)
C6	0.2364 (3)	0.9992 (2)	0.1961 (2)	0.0635 (7)
C7	0.2840 (2)	0.9991 (2)	0.3080 (2)	0.0543 (6)
C8	0.2758 (2)	0.8720 (2)	0.3627 (2)	0.0430 (5)
C9	0.3277 (2)	0.8730 (2)	0.4787 (2)	0.0473 (5)
C10	0.3245 (2)	0.7510 (2)	0.53063 (19)	0.0465 (5)
C11	0.2644 (2)	0.6220 (2)	0.46756 (18)	0.0403 (4)
C12	0.2041 (2)	0.3771 (2)	0.48333 (18)	0.0406 (5)
C13	0.1397 (2)	0.3577 (2)	0.37734 (19)	0.0431 (5)
C14	0.2173 (2)	0.2685 (2)	0.56609 (18)	0.0401 (4)
C15	0.0923 (2)	0.1769 (2)	0.5723 (2)	0.0542 (6)
C16	0.1045 (2)	0.0765 (2)	0.6511 (2)	0.0609 (7)
C17	0.2428 (3)	0.0687 (2)	0.7219 (2)	0.0532 (6)
C18	0.3693 (2)	0.1574 (2)	0.7168 (2)	0.0538 (6)
C19	0.3551 (2)	0.2575 (2)	0.63937 (19)	0.0483 (5)
C20	0.2310 (2)	0.4205 (2)	0.21085 (17)	0.0419 (5)
C21	0.1736 (3)	0.3746 (2)	0.09965 (19)	0.0542 (6)
C22	0.2691 (3)	0.3322 (2)	0.0309 (2)	0.0618 (7)
C23	0.4242 (3)	0.3367 (2)	0.0735 (2)	0.0571 (6)
C24	0.4842 (2)	0.3788 (2)	0.1839 (2)	0.0547 (6)
C25	0.3879 (2)	0.4192 (2)	0.25085 (19)	0.0475 (5)
C26	−0.0378 (2)	0.4756 (2)	0.2390 (2)	0.0551 (6)
H4	0.1309	0.6630	0.1389	0.063*
H5	0.1474	0.8717	0.0556	0.074*
H6	0.2420	1.0839	0.1619	0.076*
H7	0.3229	1.0842	0.3498	0.065*
H9	0.3648	0.9586	0.5202	0.057*
H10	0.3615	0.7523	0.6071	0.056*
H13	0.0939	0.2670	0.3510	0.052*
H15	−0.0010	0.1823	0.5234	0.065*
H16	0.0198	0.0156	0.6555	0.073*
H18	0.4629	0.1501	0.7649	0.065*
H19	0.4400	0.3190	0.6363	0.058*
H21	0.0688	0.3724	0.0707	0.065*
H22	0.2287	0.3010	−0.0432	0.074*
H24	0.5889	0.3798	0.2127	0.066*
H25	0.4289	0.4468	0.3256	0.057*
H261	−0.0469	0.5428	0.1831	0.066*
H262	−0.0806	0.3831	0.2052	0.066*
H263	−0.0921	0.5047	0.2948	0.066*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
Cl1	0.1224 (7)	0.0753 (5)	0.0833 (5)	0.0203 (4)	0.0317 (5)	0.0476 (4)
Cl2	0.1234 (7)	0.0946 (6)	0.0600 (4)	0.0380 (5)	0.0429 (4)	0.0140 (4)
O1	0.0640 (10)	0.0346 (8)	0.0440 (8)	−0.0043 (7)	0.0019 (7)	0.0087 (6)
C1	0.0442 (12)	0.0305 (10)	0.0439 (11)	0.0003 (9)	0.0033 (9)	0.0046 (8)
C2	0.0383 (11)	0.0323 (11)	0.0446 (11)	0.0043 (9)	0.0101 (9)	0.0065 (9)
C3	0.0414 (11)	0.0340 (11)	0.0490 (12)	0.0066 (9)	0.0127 (10)	0.0096 (9)
C4	0.0627 (15)	0.0421 (13)	0.0529 (14)	0.0086 (11)	0.0117 (12)	0.0126 (10)
C5	0.0797 (19)	0.0519 (15)	0.0579 (15)	0.0144 (13)	0.0186 (14)	0.0216 (12)
C6	0.0733 (18)	0.0409 (14)	0.085 (2)	0.0116 (13)	0.0274 (15)	0.0283 (13)
C7	0.0544 (14)	0.0338 (12)	0.0771 (18)	0.0028 (10)	0.0179 (13)	0.0117 (11)
C8	0.0401 (11)	0.0315 (11)	0.0598 (14)	0.0037 (9)	0.0150 (10)	0.0062 (9)
C9	0.0452 (13)	0.0346 (11)	0.0615 (14)	−0.0016 (9)	0.0131 (11)	−0.0011 (10)
C10	0.0487 (13)	0.0407 (12)	0.0469 (12)	−0.0022 (10)	0.0058 (10)	−0.0006 (10)
C11	0.0410 (11)	0.0336 (11)	0.0466 (12)	0.0017 (9)	0.0095 (10)	0.0083 (9)
C12	0.0391 (11)	0.0332 (11)	0.0493 (12)	0.0003 (9)	0.0083 (10)	0.0086 (9)
C13	0.0465 (12)	0.0311 (11)	0.0502 (13)	−0.0014 (9)	0.0075 (10)	0.0070 (9)
C14	0.0425 (12)	0.0356 (11)	0.0448 (11)	0.0046 (9)	0.0135 (10)	0.0080 (9)
C15	0.0407 (13)	0.0519 (14)	0.0718 (16)	0.0053 (11)	0.0108 (12)	0.0225 (12)
C16	0.0542 (15)	0.0499 (15)	0.0861 (19)	0.0028 (11)	0.0262 (14)	0.0271 (13)
C17	0.0697 (17)	0.0452 (13)	0.0521 (14)	0.0150 (12)	0.0220 (13)	0.0196 (11)
C18	0.0573 (15)	0.0542 (15)	0.0485 (13)	0.0079 (12)	0.0046 (11)	0.0126 (11)
C19	0.0467 (13)	0.0471 (13)	0.0496 (13)	−0.0023 (10)	0.0076 (11)	0.0084 (10)
C20	0.0541 (13)	0.0300 (10)	0.0390 (11)	0.0037 (9)	0.0031 (10)	0.0066 (8)
C21	0.0660 (16)	0.0473 (14)	0.0425 (12)	0.0097 (12)	−0.0054 (11)	0.0039 (10)
C22	0.093 (2)	0.0555 (16)	0.0343 (12)	0.0178 (14)	0.0038 (13)	0.0045 (10)
C23	0.087 (2)	0.0459 (14)	0.0441 (13)	0.0187 (13)	0.0209 (13)	0.0105 (10)
C24	0.0596 (15)	0.0562 (15)	0.0498 (14)	0.0118 (12)	0.0125 (12)	0.0057 (11)
C25	0.0542 (14)	0.0457 (13)	0.0403 (11)	0.0046 (11)	0.0058 (10)	0.0004 (9)
C26	0.0474 (14)	0.0512 (14)	0.0624 (15)	0.0012 (11)	0.0015 (11)	0.0098 (11)

Geometric parameters (Å, º) top

Cl1—C17	1.743 (2)	C18—C19	1.378 (3)
Cl2—C23	1.740 (3)	C20—C21	1.389 (2)
O1—C11	1.385 (2)	C20—C25	1.389 (3)
O1—C12	1.381 (2)	C21—C22	1.386 (4)
C1—C2	1.536 (2)	C22—C23	1.375 (4)
C1—C13	1.517 (3)	C23—C24	1.375 (3)
C1—C20	1.547 (3)	C24—C25	1.371 (3)
C1—C26	1.542 (3)	C4—H4	0.930
C2—C3	1.446 (3)	C5—H5	0.930
C2—C11	1.367 (2)	C6—H6	0.930
C3—C4	1.415 (3)	C7—H7	0.930
C3—C8	1.424 (2)	C9—H9	0.930
C4—C5	1.373 (3)	C10—H10	0.930
C5—C6	1.397 (3)	C13—H13	0.930
C6—C7	1.356 (4)	C15—H15	0.930
C7—C8	1.416 (3)	C16—H16	0.930
C8—C9	1.407 (3)	C18—H18	0.930
C9—C10	1.353 (3)	C19—H19	0.930
C10—C11	1.411 (2)	C21—H21	0.930
C12—C13	1.308 (2)	C22—H22	0.930
C12—C14	1.484 (3)	C24—H24	0.930
C14—C15	1.381 (3)	C25—H25	0.930
C14—C19	1.383 (2)	C26—H261	0.960
C15—C16	1.391 (3)	C26—H262	0.960
C16—C17	1.368 (3)	C26—H263	0.960
C17—C18	1.372 (3)

C11—O1—C12	117.40 (15)	C21—C22—C23	119.3 (2)
C2—C1—C13	108.24 (16)	Cl2—C23—C22	120.80 (18)
C2—C1—C20	109.59 (17)	Cl2—C23—C24	118.6 (2)
C2—C1—C26	111.80 (18)	C22—C23—C24	120.6 (2)
C13—C1—C20	106.20 (17)	C23—C24—C25	119.3 (2)
C13—C1—C26	106.86 (18)	C20—C25—C24	122.2 (2)
C20—C1—C26	113.82 (17)	C3—C4—H4	119.0
C1—C2—C3	122.33 (17)	C5—C4—H4	119.0
C1—C2—C11	120.91 (18)	C4—C5—H5	119.8
C3—C2—C11	116.76 (17)	C6—C5—H5	119.8
C2—C3—C4	123.51 (18)	C5—C6—H6	120.1
C2—C3—C8	119.56 (19)	C7—C6—H6	120.1
C4—C3—C8	116.9 (2)	C6—C7—H7	119.3
C3—C4—C5	121.9 (2)	C8—C7—H7	119.3
C4—C5—C6	120.3 (2)	C8—C9—H9	119.5
C5—C6—C7	119.8 (2)	C10—C9—H9	119.5
C6—C7—C8	121.4 (2)	C9—C10—H10	120.4
C3—C8—C7	119.6 (2)	C11—C10—H10	120.4
C3—C8—C9	119.6 (2)	C1—C13—H13	116.9
C7—C8—C9	120.82 (19)	C12—C13—H13	116.9
C8—C9—C10	120.91 (19)	C14—C15—H15	119.6
C9—C10—C11	119.3 (2)	C16—C15—H15	119.6
O1—C11—C2	124.47 (17)	C15—C16—H16	120.5
O1—C11—C10	111.76 (17)	C17—C16—H16	120.5
C2—C11—C10	123.8 (2)	C17—C18—H18	120.6
O1—C12—C13	122.56 (19)	C19—C18—H18	120.6
O1—C12—C14	110.38 (16)	C14—C19—H19	119.3
C13—C12—C14	127.05 (18)	C18—C19—H19	119.3
C1—C13—C12	126.12 (19)	C20—C21—H21	119.3
C12—C14—C15	120.82 (19)	C22—C21—H21	119.3
C12—C14—C19	120.67 (19)	C21—C22—H22	120.4
C15—C14—C19	118.5 (2)	C23—C22—H22	120.4
C14—C15—C16	120.7 (2)	C23—C24—H24	120.4
C15—C16—C17	119.1 (2)	C25—C24—H24	120.4
Cl1—C17—C16	119.3 (2)	C20—C25—H25	118.9
Cl1—C17—C18	119.22 (18)	C24—C25—H25	118.9
C16—C17—C18	121.5 (2)	C1—C26—H261	109.5
C17—C18—C19	118.9 (2)	C1—C26—H262	109.5
C14—C19—C18	121.4 (2)	C1—C26—H263	109.5
C1—C20—C21	124.8 (2)	H261—C26—H262	109.5
C1—C20—C25	118.00 (17)	H261—C26—H263	109.5
C21—C20—C25	117.2 (2)	H262—C26—H263	109.5
C20—C21—C22	121.4 (2)

C11—O1—C12—C13	3.5 (3)	C5—C6—C7—C8	−0.5 (4)
C11—O1—C12—C14	−177.32 (19)	C6—C7—C8—C3	−0.9 (3)
C12—O1—C11—C2	−6.0 (3)	C6—C7—C8—C9	179.0 (2)
C12—O1—C11—C10	173.84 (19)	C3—C8—C9—C10	2.0 (3)
C2—C1—C13—C12	−3.8 (3)	C7—C8—C9—C10	−177.9 (2)
C13—C1—C2—C3	−179.1 (2)	C8—C9—C10—C11	−1.7 (3)
C13—C1—C2—C11	1.3 (2)	C9—C10—C11—O1	178.7 (2)
C2—C1—C20—C21	−131.0 (2)	C9—C10—C11—C2	−1.5 (3)
C2—C1—C20—C25	50.4 (2)	O1—C12—C13—C1	1.6 (3)
C20—C1—C2—C3	65.5 (2)	O1—C12—C14—C15	133.8 (2)
C20—C1—C2—C11	−114.1 (2)	O1—C12—C14—C19	−45.6 (2)
C26—C1—C2—C3	−61.6 (2)	C13—C12—C14—C15	−47.0 (3)
C26—C1—C2—C11	118.8 (2)	C13—C12—C14—C19	133.5 (2)
C13—C1—C20—C21	112.3 (2)	C14—C12—C13—C1	−177.5 (2)
C13—C1—C20—C25	−66.3 (2)	C12—C14—C15—C16	−179.0 (2)
C20—C1—C13—C12	113.8 (2)	C12—C14—C19—C18	179.9 (2)
C26—C1—C13—C12	−124.4 (2)	C15—C14—C19—C18	0.4 (3)
C26—C1—C20—C21	−5.0 (3)	C19—C14—C15—C16	0.4 (3)
C26—C1—C20—C25	176.4 (2)	C14—C15—C16—C17	−0.6 (4)
C1—C2—C3—C4	−4.6 (3)	C15—C16—C17—Cl1	−179.6 (2)
C1—C2—C3—C8	176.9 (2)	C15—C16—C17—C18	−0.0 (3)
C1—C2—C11—O1	3.4 (3)	Cl1—C17—C18—C19	−179.58 (19)
C1—C2—C11—C10	−176.4 (2)	C16—C17—C18—C19	0.8 (3)
C3—C2—C11—O1	−176.2 (2)	C17—C18—C19—C14	−1.0 (3)
C3—C2—C11—C10	4.0 (3)	C1—C20—C21—C22	−179.8 (2)
C11—C2—C3—C4	175.1 (2)	C1—C20—C25—C24	−179.5 (2)
C11—C2—C3—C8	−3.4 (3)	C21—C20—C25—C24	1.8 (3)
C2—C3—C4—C5	179.8 (2)	C25—C20—C21—C22	−1.2 (3)
C2—C3—C8—C7	−179.5 (2)	C20—C21—C22—C23	−0.6 (3)
C2—C3—C8—C9	0.6 (3)	C21—C22—C23—Cl2	−177.82 (19)
C4—C3—C8—C7	1.9 (3)	C21—C22—C23—C24	1.9 (3)
C4—C3—C8—C9	−178.0 (2)	Cl2—C23—C24—C25	178.40 (19)
C8—C3—C4—C5	−1.7 (3)	C22—C23—C24—C25	−1.3 (3)
C3—C4—C5—C6	0.4 (4)	C23—C24—C25—C20	−0.6 (3)
C4—C5—C6—C7	0.7 (4)

Experimental details

Crystal data
Chemical formula	C₂₆H₁₈Cl₂O
M_r	417.33
Crystal system, space group	Triclinic, P1
Temperature (K)	296
a, b, c (Å)	8.9554 (6), 9.4439 (6), 12.3206 (7)
α, β, γ (°)	93.511 (2), 102.0453 (15), 94.287 (2)
V (Å³)	1013.05 (11)
Z	2
Radiation type	Mo Kα
µ (mm⁻¹)	0.34
Crystal size (mm)	0.42 × 0.37 × 0.28

Data collection
Diffractometer	Rigaku R-AXIS RAPID diffractometer
Absorption correction	Multi-scan (ABSCOR; Higashi, 1995)
T_min, T_max	0.874, 0.910
No. of measured, independent and observed [F² > 2σ(F²)] reflections	10050, 4596, 2783
R_int	0.021
(sin θ/λ)_max (Å⁻¹)	0.649

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.042, 0.095, 1.00
No. of reflections	4596
No. of parameters	264
No. of restraints	?
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	0.28, −0.33

Computer programs: PROCESS-AUTO (Rigaku, 1998), CrystalStructure (Rigaku/MSC, 2004), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), ORTEP-3 for Windows (Farrugia, 1997).

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1,3-Bis(4-chloro­phen­yl)-1-methyl-1H-benzo[f]chromene

Supporting information

Key indicators

checkCIF/PLATON results

1,3-Bis(4-chlorophenyl)-1-methyl-1H-benzo[f]chromene