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Isoquinoline, 1-chloro-3,4-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102183-41-5

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102183-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102183-41-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,1,8 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 102183-41:
(8*1)+(7*0)+(6*2)+(5*1)+(4*8)+(3*3)+(2*4)+(1*1)=75
75 % 10 = 5
So 102183-41-5 is a valid CAS Registry Number.

102183-41-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Chloro-3,4-diphenylisoquinoline

1.2 Other means of identification

Product number -
Other names 1-chloro-3,4-diphenyl-isoquinoline

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:102183-41-5 SDS

102183-41-5Downstream Products

102183-41-5Relevant academic research and scientific papers

SYNTHESIS OF 1-SUBSTITUTED 3,4-DIARYLISOQUINOLINE DERIVATIVES

Delcey, Martine Croisy,Huel, Christiane,Bisagni, Emile

, p. 1721 - 1730 (2007/10/03)

3,4-Diaryl-2H-isoquinolin-2-ones and corresponding 1-chloro derivatives were easily prepared in a way involving i) condensation of 2-aroylbenzyl chlorides with arylmethylamines; ii) treatment of the resulting 1-aryl-N-1-hydroxyarylmethylisoindol-3-ones wi

Synthesis of Isoquinolines by Cycloaddition of Arynes to 1,2,4-Triazines

Gonsalves, Antonio M. d'A. Rocha,Melo, Teresa M. V. D. Pinho e

, p. 6821 - 6826 (2007/10/02)

Benzyne has been generated from benzenediazonium-2-carboxylate in the presence of several 1,2,4-triazines 1 and isoquinolines 2 have been isolated in moderate yield. 1-Aminobenzotriazole was also used as the source of benzyne and isoquinolines were again isolated in moderate yield from these reactions. 4-Methylbenzyne, which was generated from 5-methylanthranilic acid, reacted unselectively with the triazines to give mixtures of 6- and 7-methylisoquinolines 3 and 4.On the other hand reactions of 3-methylbenzyne with the triazines 1d and 1e proceeded with high regioselectivity, giving only the 5-methylisoquinoline 5a and the 8-methylisoquinoline 6b, respectively.

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