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161144

Sigma-Aldrich

Biphenyl-4-carbonyl chloride

97%

Synonym(s):

4-Phenylbenzoyl chloride

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About This Item

Linear Formula:
C6H5C6H4COCl
CAS Number:
14002-51-8
Molecular Weight:
216.66
Beilstein:
472842
EC Number:
237-804-8
MDL number:
MFCD00000692
UNSPSC Code:
12352100
PubChem Substance ID:
24849907
NACRES:
NA.22

Assay

97%

mp

110-112 °C (lit.)

functional group

acyl chloride

SMILES string

ClC(=O)c1ccc(cc1)-c2ccccc2

InChI

1S/C13H9ClO/c14-13(15)12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9H

InChI key

JPVUWCPKMYXOKW-UHFFFAOYSA-N

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Application

Biphenyl-4-carbonyl chloride was used in the preparation of a novel thiourea compound, N-(6-methyl pyridin-2-yl-carbamothioyl)biphenyl-4-carboxamide. It was also used in the preparation of 5-CF3-oxazole analog, 2-{4-[2-(2-biphenyl-4-yl-5-trifluoromethyl-oxazol-4-yl)-ethoxy]-phenoxy}-2-methyl-propionic acid.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
STBH0943
STBH9492
STBJ2294
STBH9734
STBG0778V

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Theoretical and experimental studies on N-(6-methylpyridin-2-yl-carbamothioyl) biphenyl-4-carboxamide.
Yesilkaynak T, et al.
European Journal of Chemistry, 1(1), 1-5 (2010)
Alexander G Godfrey et al.
The Journal of organic chemistry, 68(7), 2623-2632 (2003-03-29)
An improved method for the preparation of a series of oxazole-containing dual PPARalpha/gamma agonists is described. A synthetic sequence utilizing a Dakin-West reaction was devised that allows for the introduction of the oxazole ring either late in the synthetic sequence

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