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55320-82-6

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55320-82-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55320-82-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,3,2 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 55320-82:
(7*5)+(6*5)+(5*3)+(4*2)+(3*0)+(2*8)+(1*2)=106
106 % 10 = 6
So 55320-82-6 is a valid CAS Registry Number.

55320-82-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-diphenyl-2-propylimidazolidine

1.2 Other means of identification

Product number -
Other names Imidazolidine,1,3-diphenyl-2-propyl

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:55320-82-6 SDS

55320-82-6Downstream Products

55320-82-6Relevant articles and documents

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone, a Mild Catalyst for the Formation of Carbon-Nitrogen Bonds

Eynde, Jean Jacques Vanden,Delfosse, Florence,Lor, Pascal,Haverbeke, Yves Van

, p. 5813 - 5818 (2007/10/02)

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) catalyzes the preparation of N-tetrahydropyranylbenzazoles, 2-substituted 1,3-diphenylimidazolidines, and N-(arylmethylene)benzene-1,2-diamines.In the latter case, use of one equivalent of DDQ provides a novel one-pot method for the synthesis of 1H-benzimidazoles.

NOVEL SYNTHESES OF HETEROCYCLES WITH N-(1-HALOALKYL)AZINIUM HALIDES PART 1. PREPARATION OF IMIDAZOLIDINES

Eynde, J.-J. Vanden,Mayence, A.,Maquestiau, A.,Anders, E.

, p. 233 - 236 (2007/10/02)

N-(1-Chloroalkyl)pyridinium chlorides, prepared from thionyl chloride, pyridine, and an aldehyde, readily react with N,N'-disubstituted 1,2-ethanediamine to yield imidazolidines under mild and neutral conditions.

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