4-CHLORODIPHENYLMETHANE
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4-CHLORODIPHENYLMETHANE
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CAS No:
831-81-2
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Formula:
C13H11Cl
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Chemical Name:
4-CHLORODIPHENYLMETHANE
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Synonyms:
NSC 83166;4-chloroditan;p-chlorobenzylbenzene;4-Benzylchlorobenzene;4-CHLORODIPHENYLMETHANE;p-chlorodiphenylmethane;1-(benzyl)-4-chloro-benzene;(p-chlorophenyl)phenylmethane;(p-chlorophenyl)phenyl-methan;(4-chlorophenyl)phenylmethane
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CAS No:
4-CHLORODIPHENYLMETHANE Basic Attributes
202.681
202.05500
DF8MF37RDF
83166
DTXSID1073238
2903999090
Characteristics
0
4.9
1.1247 @ 20 DEG C/20 DEG C
7.5 DEG C
298 DEG C @ 742 MM HG
122ºC
1.583
INSOL IN WATER, SOL IN ACETONE
Safety Information
Xi: Irritant;
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
H315
|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 2 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
4-CHLORODIPHENYLMETHANE Use and Manufacturing
General procedure: To a solution of Ph3PO (0.33 g, 1.2 mmol) in CH2Cl2 (1 mL), Tf2O (0.2 mL, 1.2 mmol) was added at 0 C and the solution was stirred for 15 min at room temperature. Then, arene (1 mmol) and benzyl alcohol (1 mmol) were added to the reaction mixture and the mixture was stirred for the appropriate time shown in Table 1 and Table 2. Upon completion of the reaction, the organic solvent was evaporated and the crude product was purified by column chromatography using n-hexane as eluent to give the diarylmethane. In the case of 4-nitrobenzyl alcohol, EtOAc/n-hexane (1:9) was used as the eluent.General procedure: A round-bottomed flask equipped with a condenser was charged with benzyl chloride (0.5 mmol), arylboronic acid (0.6 mmol), base (0.75 mmol), Pd(II) catalyst (3 mol%) and the mixture was stirred in 5 mL of solvent at 90 C for the required time. After completion, the reaction mixture was diluted with ether (10 mL), water (10 mL) and extracted with ether (3 ×10 mL). The combined extract was dried over MgSO4. After evaporation of the solvent under reduced pressure, the residue was purified by column chromatography to obtain the desired products.General procedure: A round-bottomed flask equipped with a condenser was charged with benzyl chloride (0.5 mmol), aryl boronic acid (0.6 mmol), base (1.0 mmol), PdCl2 (1.0 mol%) and the mixture was stirred in 5 mL of solvent at 90 C for the required time. After completion, the reaction mixture was diluted with ether (10 mL), water (10 mL) and extracted with ether (3 × 10 mL). The combined extract was dried over anhydrous Na2SO4. After evaporation of the solvent under reduced pressure, the residue was purified by column chromatography to obtain the desired products.
Computed Properties
Molecular Weight:202.68
XLogP3:4.9
Rotatable Bond Count:2
Exact Mass:202.0549280
Monoisotopic Mass:202.0549280
Heavy Atom Count:14
Complexity:153
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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