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2-Propenoic acid, 2-methyl-, 2-(methylphenylamino)ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52234-98-7

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52234-98-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52234-98-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,2,3 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52234-98:
(7*5)+(6*2)+(5*2)+(4*3)+(3*4)+(2*9)+(1*8)=107
107 % 10 = 7
So 52234-98-7 is a valid CAS Registry Number.

52234-98-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(N-methylanilino)ethyl 2-methylprop-2-enoate

1.2 Other means of identification

Product number -
Other names 2-Propenoic acid,2-methyl-,2-(methylphenylamino)ethyl ester

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:52234-98-7 SDS

52234-98-7Relevant academic research and scientific papers

New photosensitive methacrylate monomers with 4-aminoazobenzene type chromophore group

Janik,Kucharski,Kubainska,Lyko

, p. 241 - 252 (2007/10/03)

Photosensitive methacrylate monomers, derivatives of azobenzene, were synthesized. The route of syntheses was based on coupling of diazonium salts of sulfathiazole, sulfomethoxazole, sulfadiazine, 4-aminobenzoic acid and 4-nitroaniline with N-alkyl-N-[2-(methacryloyloxy)ethyl]aniline. The trans?cis isomerization of the monomers in DMSO solution was investigated by UV-VIS spectroscopy recording their spectra during illumination and thermal recovery periods. It was found that except for nitro derivatives the yield of trans-cis isomerization was ca. 50% and that the reverse reaction was a result of thermal relaxation. The spectroscopic studies were accompanied by quantum chemical calculations.

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