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67245-09-4

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67245-09-4 Usage

General Description

The chemical (2E)-N-benzyl-2-cyano-2-(hydroxyimino)ethanamide, also known as benzyl cyanooxime, is an organic compound with the molecular formula C10H11N3O. It is a derivative of oxime and is commonly used in organic synthesis and as a reagent in various chemical reactions. (2E)-N-benzyl-2-cyano-2-(hydroxyimino)ethanamide is a white to pale yellow solid at room temperature and is slightly soluble in water. It has a variety of applications in the pharmaceutical and chemical industries, including as a building block for the synthesis of pharmaceuticals and agrochemicals. Additionally, it can also be used as a ligand in coordination chemistry. Overall, (2E)-N-benzyl-2-cyano-2-(hydroxyimino)ethanamide is an important chemical with diverse applications in organic synthesis and chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 67245-09-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,2,4 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 67245-09:
(7*6)+(6*7)+(5*2)+(4*4)+(3*5)+(2*0)+(1*9)=134
134 % 10 = 4
So 67245-09-4 is a valid CAS Registry Number.

67245-09-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-2-cyano-2-hydroxyiminoacetamide

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

1.4 Supplier's details

1.5 Emergency phone number

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More Details:67245-09-4 SDS

67245-09-4Upstream product

67245-09-4Relevant articles and documents

Heterocyclization of compounds containing diazo and cyano groups. 6. Theoretical and experimental investigations of cyclization of 2-cyano-2-diazoacetamides to 5-hydroxy-1,2,3-triazole-4-carbonitriles

Morzherin,Kolobov,Mokrushin,Brauer,Anders,Bakulev

, p. 22 - 36 (2007/10/03)

A series of N-alkyl- and N-aryl-2-cyano-2-diazoacetamides was synthesized by the reaction of 2-amino-2-cyanoacetamides with sodium nitrite in hydrochloric acid. The mechanism of their heteroelectrocyclization to 5-hydroxy-1,2,3-triazoles was investigated

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