331589
Diphenylacetyl chloride
90%, technical grade
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
(C6H5)2CHCOCl
CAS Number:
Molecular Weight:
230.69
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
217-493-5
MDL number:
Assay:
90%
Form:
solid
Product Name
Diphenylacetyl chloride, 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.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class
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
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service