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Ethyl 4-cyano-2-oxo-4,4-diphenylbutanoate is a chemical compound with the molecular formula C18H17NO3. It is a derivative of 4-cyano-2-oxo-4,4-diphenylbutanoic acid, featuring an ethyl ester group attached to the carboxylic acid moiety. This organic compound is characterized by its cyano group (-CN), which imparts a strong, pungent odor, and its diphenylbutanoate structure, which consists of two phenyl rings attached to a butanoate chain. The compound is used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically synthesized through a series of chemical reactions involving esterification and cyanation processes. Ethyl 4-cyano-2-oxo-4,4-diphenylbutanoate is an important intermediate in the production of certain drugs and pesticides, highlighting its significance in the chemical industry.

3122-22-3

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3122-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3122-22-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,2 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3122-22:
(6*3)+(5*1)+(4*2)+(3*2)+(2*2)+(1*2)=43
43 % 10 = 3
So 3122-22-3 is a valid CAS Registry Number.

3122-22-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Oxo-3,3-diphenyl-bernsteinsaeure-1-ethylester-4-nitril

1.2 Other means of identification

Product number -
Other names Ethyl 4-cyano-2-oxo-4,4-diphenylbutanoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3122-22-3 SDS

3122-22-3Downstream Products

3122-22-3Relevant academic research and scientific papers

Reactions of Triphenylphosphine- and Trialkyl Phosphite-Silver Nitrate Complexes with Positive Halogen Compounds. Synthesis of α-Nitro Nitriles

Ketari, Rachid,Foucaud, Andre

, p. 4498 - 4501 (2007/10/02)

The reaction of α-bromo-α-cyano esters, α-bromo-α-cyano nitriles, and α-bromo-α-cyano imides with triphenylphosphine- or trialkyl phosphite-silver nitrate complexes leads to replacement of the positive bromine atom by a nitro group under mild conditions.I

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