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Cyano(3-nitrophenyl)methyl benzoate is a chemical compound with the molecular formula C15H10N2O4. It is an organic compound that features a benzoate group (a benzene ring with a carboxylate group) and a cyano(3-nitrophenyl)methyl group, which consists of a nitro group (-NO2) attached to a phenyl ring and a cyano group (-CN) connected to a methylene bridge. cyano(3-nitrophenyl)methyl benzoate is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is also used as an intermediate in the preparation of certain dyes and pigments. The compound's properties, such as its solubility and stability, can be influenced by the presence of the nitro and cyano groups, making it a versatile building block in organic synthesis.

7252-27-9

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7252-27-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7252-27-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,5 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7252-27:
(6*7)+(5*2)+(4*5)+(3*2)+(2*2)+(1*7)=89
89 % 10 = 9
So 7252-27-9 is a valid CAS Registry Number.

7252-27-9SDS

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 [cyano-(3-nitrophenyl)methyl] benzoate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

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

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More Details:7252-27-9 SDS

7252-27-9Relevant academic research and scientific papers

A Simple One-Pot Synthesis of Silylated and Acylated Cyanohydrins

Yoneda, Ryuji,Santo, Kazunori,Harusawa, Shinya,Kurihara, Takushi

, p. 1054 - 1055 (2007/10/02)

Reaction of variety of aldehydes and ketones with chlorotrimethylsilane and acyl chlorides in the presence of lithium cyanide to give trimethylsilylcyanohydrins and acylcyanohydrins is described.

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