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1-methyl-2-phenylimidazolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53370-26-6

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53370-26-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53370-26-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,7 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53370-26:
(7*5)+(6*3)+(5*3)+(4*7)+(3*0)+(2*2)+(1*6)=106
106 % 10 = 6
So 53370-26-6 is a valid CAS Registry Number.

53370-26-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-2-phenylimidazolidine

1.2 Other means of identification

Product number -
Other names IMIDAZOLIDINE,1-METHYL-2-PHENYL

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:53370-26-6 SDS

53370-26-6Downstream Products

53370-26-6Relevant academic research and scientific papers

Comparative radioprotective activity of various pentagonal compounds with two heteroatomes

Robbe,Fernandez,Dubief,et al.

, p. 235 - 243 (2007/10/02)

Various heterocyclic compounds with two heteroatomes were synthesized and their potential radioprotective activity was tested. This study shows the interest of phenylthiazolidines derivatives in chemical radioprotection.

RING-CHAIN TAUTOMERISM OF IMIDAZOLIDINE SYSTEM

Witek, Stanislaw,Bielawska, Alicja,Bielawski, Jacek

, p. 1313 - 1317 (2007/10/02)

The existance of the tautomeric equilibrium of imidazolidine system 34has been established.Due to a higher reactivity of NH group in 4, the reaction of the system 34 with PhNCO unbalances the tautomeric equilibrium, and causes an increase in the content of the open-chain urea derivative 6 in the reaction mixture.The use of isocyanates or other similar reagents, e.g., isothiocyanates, seems to be a convenient method for studies of the tautomerism in similar system.

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