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2-Cyanobutan-2-yl acetate, also known as 2-(2-cyanoethyl) acetate or 2-acetoxybutanenitrile, is an organic compound with the chemical formula C6H9NO2. It is a colorless liquid with a molecular weight of 127.14 g/mol. 2-cyanobutan-2-yl acetate is characterized by the presence of a nitrile group (-CN) and an ester group (-COO-), which are connected to a butane chain with a double bond between the second and third carbon atoms. 2-Cyanobutan-2-yl acetate is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its potential applications in the production of polymers and as a solvent. Due to its reactivity, it is important to handle 2-cyanobutan-2-yl acetate with care, following appropriate safety measures.

5401-57-0

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5401-57-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5401-57-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,0 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5401-57:
(6*5)+(5*4)+(4*0)+(3*1)+(2*5)+(1*7)=70
70 % 10 = 0
So 5401-57-0 is a valid CAS Registry Number.

5401-57-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-cyanobutan-2-yl acetate

1.2 Other means of identification

Product number -
Other names 2-HYDROXY-2-METHYLBUTYRONITRILE ACETATE

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:5401-57-0 SDS

5401-57-0Downstream Products

5401-57-0Relevant academic research and scientific papers

ENZYMATIC KINETIC RESOLUTION OF CYANOHYDRIN ACETATES AND ITS APPLICATION TO THE SYNTHESIS OF (S)-(-)-FRONTALIN

Ohta, Hiromichi,Kimura, Yoichi,Sugano, Yasushi,Sugai, Takeshi

, p. 5469 - 5476 (2007/10/02)

Kinetic resolution of racemic 1-cyano-1-methylalkyl and alkenyl acetates has been achieved on incubation with Pichia miso IAM 4682, which hydrolyzed selectively the (R)-enantiomer, leving behind the (S)-enantiomer intact.The chiral 1-cyano-1-methyl-5-hexenyl acetate thus obtained was converted to (S)-frontalin via unsaturated diol.

KINETIC RESOLUTION OF KETONE CYANOHYDRIN ACETATES WITH A MICROBIAL ENZYME

Ohta, Hiromichi,Kimura,Yoichi,Sugano, Yasushi

, p. 6957 - 6960 (2007/10/02)

Incubation of dl-1-cyano-1-metylalkyl (or alkenyl) acatates (methyl ketone cyanohydrin acetates) with cells of Pichia miso IAM 4682 afforded optically active acetates and the corresponding ketones via asymmetric hydrolysis.Resulting (S)-2-cyano-2-undecyl acetate was converted to the aminofuranone derivative without losing its optical purity.

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