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Benzeneacetic acid, 1-(phenylmethyl)hydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112157-90-1

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112157-90-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112157-90-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,1,5 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 112157-90:
(8*1)+(7*1)+(6*2)+(5*1)+(4*5)+(3*7)+(2*9)+(1*0)=91
91 % 10 = 1
So 112157-90-1 is a valid CAS Registry Number.

112157-90-1SDS

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-phenylacetohydrazide

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:112157-90-1 SDS

112157-90-1Downstream Products

112157-90-1Relevant academic research and scientific papers

Optodynamers: Expression of color and fluorescence at the interface between two films of different dynamic polymers

Ono, Takashi,Fujii, Shunsuke,Nobori, Tadahito,Lehn, Jean-Marie

, p. 4360 - 4362 (2008/04/01)

Color and fluorescence changes were expressed at the interface between two different polyhydrazone polymer films, induced by hydrazone bond exchange and component recombination through the interface, resulting in an extension of conjugation. The Royal Society of Chemistry.

NEW SYNTHETIC "TRICKS". FROM ALIPHATIC AMINES AND AMIDES TO AZIDES AND/OR HOW TO CONVERT RNHCOR' INTO RNHCOR" AVOIDING DRASTIC HYDROLYSES

Garcia, Jordi,Vilarrasa, Jaume

, p. 341 - 342 (2007/10/02)

Controlled reduction of N-alkyl-N-nitrosoamides to hydrazides followed by nitrosation and fragmentation affords azides in 80percent overall yields, under mild conditions.This simple idea is the basis of methods for the conversion of alkylamines and N-alkylamides to alkyl azides, of RNHCOR' into RNHCOR" or RN(COR''')2, and of lactames into ω-azido esters or ω-azido acids.

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