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Pyridazino[1,6-a]benzimidazole, 2,4-dimethyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81889-93-2

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81889-93-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81889-93-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,8,8 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 81889-93:
(7*8)+(6*1)+(5*8)+(4*8)+(3*9)+(2*9)+(1*3)=182
182 % 10 = 2
So 81889-93-2 is a valid CAS Registry Number.

81889-93-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dimethylpyridazino<1,6-a>benzimidazole

1.2 Other means of identification

Product number -
Other names 2,4-Dimethyl-benzo[4,5]imidazo[1,2-b]pyridazine

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:81889-93-2 SDS

81889-93-2Downstream Products

81889-93-2Relevant academic research and scientific papers

Reactions of a series of 1-aminobenzimidazoles and 1-amino-3- methylbenzimidazolium chlorides with 2,4-pentanedione

Kaiya, Toyo,Aoyama, Shinsuke,Kohda, Kohfuku

, p. 37 - 42 (2007/10/03)

Reactions of a series of 1-aminobenzimidazoles and 1-amino-3- methylbenzimidazolium chlorides with 2,4-pentanedione were carried out and pyridazino[1,6-a]benzimidazoles and 2-pyrazolylanilines were generated. The product ratios of these compounds remarkably depended on the reaction conditions and on the electronic character of the substituent at the benzene moiety. The possible mechanisms involved in these reactions are discussed. (C) 2000 Elsevier Science Ltd.

REACTION OF 1-AMINOBENZIMIDAZOLES WITH β-DIKETONES. SYNTHESIS OF PYRIDAZINOBENZIMIDAZOLES

Kuz'menko, V. V.,Komissarov, V. N.,Simonov, A. M.

, p. 314 - 318 (2007/10/02)

The action of acetyl- and benzoylacetone on 1-aminobenzimidazoles in the presence of catalytic amounts of zinc chloride was used to synthesize 1-ylidene derivatives, which at higher temperatures undergo thermal cyclization to 2,4-disubstituted pyridazinobenzimidazoles.

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