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Benzoic acid, 4-nitro-, cyclopentylidenehydrazide is a chemical compound with the molecular formula C13H14N4O3. It is a derivative of benzoic acid, featuring a nitro group at the 4-position and a cyclopentylidenehydrazide group attached to the carboxylic acid. Benzoic acid, 4-nitro-, cyclopentylidenehydrazide is known for its potential applications in pharmaceutical research, particularly as an intermediate in the synthesis of various drugs and medicinal agents. Its structure provides a unique combination of functional groups, which can be further modified or reacted to yield a range of bioactive molecules. The compound's properties, such as its reactivity and stability, make it a valuable component in the development of new therapeutics and chemical entities.

329-83-9

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329-83-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 329-83-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 329-83:
(5*3)+(4*2)+(3*9)+(2*8)+(1*3)=69
69 % 10 = 9
So 329-83-9 is a valid CAS Registry Number.

329-83-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(cyclopentylideneamino)-4-nitrobenzamide

1.2 Other means of identification

Product number -
Other names 4-nitro-benzoic acid cyclopentylidenehydrazide

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:329-83-9 SDS

329-83-9Relevant academic research and scientific papers

Benzoylhydrazones in catalytic hydrophosphorylation

Matveeva,Podrugina,Kolesnikova,Zefirov

experimental part, p. 411 - 417 (2011/02/17)

Reactions of benzoylhydrazones derived from heterocyclic and aromatic aldehydes and aliphatic, heterocyclic, and aliphatic-aromatic ketones with diethyl phosphite in the presence of [tetra(tert-butyl)phthalocyanine]aluminum chloride afford α-benzoylhydraz

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