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1,3-Dimethyl-2-(4-methylphenyl)imidazolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23229-38-1

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23229-38-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23229-38-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,2,2 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 23229-38:
(7*2)+(6*3)+(5*2)+(4*2)+(3*9)+(2*3)+(1*8)=91
91 % 10 = 1
So 23229-38-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H18N2/c1-10-4-6-11(7-5-10)12-13(2)8-9-14(12)3/h4-7,12H,8-9H2,1-3H3

23229-38-1SDS

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 1,3-dimethyl-2-(4-methylphenyl)imidazolidine

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:23229-38-1 SDS

23229-38-1Downstream Products

23229-38-1Relevant academic research and scientific papers

Reductive lithiation of 1,3-dimethyl-2-arylimidazolidines

Azzena, Ugo,Dettori, Giovanna,Pisano, Luisa,Siotto, Immacolata

, p. 3177 - 3182 (2007/10/03)

Naphthalene catalyzed lithiation of 1,3-dimethyl-2-phenylimidazolidine led to cleavage of the benzylic carbon-nitrogen bond, with formation of an intermediate dianion. Under similar conditions, 1,3-dimethyl-2-(4-chlorophenyl) imidazolidine underwent regioselective cleavage of the aromatic carbon-chlorine bond, leading to a 4-formylphenyllithium equivalent, whilst 1,3-dimethyl-2-(4- methoxymethylphenyl)imidazolidine underwent regioselective cleavage of the benzylic carbon-oxygen bond, leading to a 4-formylbenzyllithium equivalent.

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