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N-benzoyl-3-methoxy-benzohydrazide is a chemical compound with the molecular formula C15H13N2O3. It is a derivative of benzohydrazide, featuring a benzoyl group attached to the nitrogen atom and a methoxy group at the 3-position of the benzene ring. This white crystalline solid is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the preparation of compounds with biological activity. The compound's structure allows for further functionalization and modification, making it a valuable building block in organic chemistry.

7154-74-7

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7154-74-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7154-74-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,5 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7154-74:
(6*7)+(5*1)+(4*5)+(3*4)+(2*7)+(1*4)=97
97 % 10 = 7
So 7154-74-7 is a valid CAS Registry Number.

7154-74-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methoxy-benzoic acid N'-benzoyl-hydrazide

1.2 Other means of identification

Product number -
Other names 1-Benzoyl-2-<3-methoxy-benzoyl>-hydrazin

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:7154-74-7 SDS

7154-74-7Relevant academic research and scientific papers

1,3,4-Oxadiazole formation as traceless release in solid phase organic synthesis

Cesarini, Sara,Colombo, Nicoletta,Pulici, Maurizio,Felder, Eduard R.,Brill, Wolfgang K.-D.

, p. 10223 - 10236 (2007/10/03)

Oxadiazoles were generated upon a dehydrative cyclization reaction with 2-acyl hydrazides bound to the polymeric support via one of their N atoms using TFAA as a dehydration agent.

The Hydroxy Derivatives of 2,5-Diphenyl-1,3,4-oxadiazole

Jacobsen, Noel W.,Philippides, Athena E.

, p. 1911 - 1914 (2007/10/02)

An unambiguous synthesis for each of the monohydroxy derivatives of 2,5-diphenyl-1,3,4-oxadiazole is reported.

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