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Merck
CN

331589

二苯基乙酰氯

90%, technical grade

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关于此项目

线性分子式:
(C6H5)2CHCOCl
化学文摘社编号:
分子量:
230.69
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
217-493-5
MDL number:
Assay:
90%
Form:
solid
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产品名称

二苯基乙酰氯, 90%, technical grade

InChI key

MSYLETHDEIJMAF-UHFFFAOYSA-N

InChI

1S/C14H11ClO/c15-14(16)13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,13H

SMILES string

ClC(=O)C(c1ccccc1)c2ccccc2

grade

technical grade

assay

90%

form

solid

bp

175-176 °C/17 mmHg (lit.)

mp

49-53 °C (lit.)

Application

Diphenylacetyl chloride was used as a reagent in regioselective acylation of cyclomalto-oligosaccharides. It was also used in the preparation of N-substituted amides having local anesthetic properties.

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 2

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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F El-Zahraa et al.
Die Pharmazie, 34(1), 12-13 (1979-01-01)
Diphenylacetyl chloride and pivaloyl chloride have been condensed with a wide variety of amines. Some of the resulting amides showed local anesthetic properties higher than those of procaine hydrochloride.
Jinyeon Hwang et al.
Experimental neurology, 335, 113511-113511 (2020-10-26)
Cyclin-dependent kinase 5 (Cdk5) is involved in neural organization and synaptic functions in developing and adult brains, yet its role in axonal regeneration is not known well. Here, we characterize Cdk5 function for axonal regeneration after peripheral nerve injury. Levels
F Santoyo-González et al.
Carbohydrate research, 262(2), 271-282 (1994-09-15)
Regioselective acylation of cyclomalto-oligosaccharides was achieved using pivaloyl and diphenylacetyl chlorides. The reaction of cyclomaltohexaose (1) with pivaloyl chloride gave the hexakis(2,6-di-O-pivaloyl) derivative 19 in 66% yield. Similar reaction with cyclomalto-heptaose (2) led to the octakis(2I,6I,6II,6III,6IV,6V,6VI ,6VII-O-pivaloyl) 26 and the

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