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57042-61-2

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57042-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57042-61-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,0,4 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 57042-61:
(7*5)+(6*7)+(5*0)+(4*4)+(3*2)+(2*6)+(1*1)=112
112 % 10 = 2
So 57042-61-2 is a valid CAS Registry Number.

57042-61-2SDS

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 1-p-Methylphenyl-2-imidazolidinon

1.2 Other means of identification

Product number -
Other names 4-methyl-1-(4-nitro-benzyl)-pyridinium,bromide

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:57042-61-2 SDS

57042-61-2Relevant articles and documents

Aggregation enhanced responsiveness of rationally designed probes to hydrogen sulfide for targeted cancer imaging

Wang, Rongchen,Gu, Xianfeng,Li, Qizhao,Gao, Jie,Shi, Ben,Xu, Ge,Zhu, Tianli,Tian, He,Zhao, Chunchang

, p. 15084 - 15090 (2020)

Activatable molecular probes hold great promise for targeted cancer imaging. However, the hydrophobic nature of most conventional probes makes them generate precipitated agglomerate in aqueous media, thereby annihilating their responsiveness to analytes a

Reactions of N-benzyl-pyridinium or -isoquinolinium ylides with ethyl 3-fluoro-3-(fluoroalkyl)acrylates to give fluoroalkyl-substituted indolizine and pyrrolo[2,1-a]isoquinoline derivatives

Peng, Weimin,Zhu, Shizheng

, p. 3204 - 3210 (2007/10/03)

In the presence of base, N-benzylpyridinium and N-benzylisoquinolinium ylides generated in situ from the N-benzyl-pyridinium or -isoquinolinium bromides react with ethyl 3-fluoro-3-fluoroalkyl(except bromodifluoromethyl)acrylates to give one or two fluoro

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