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Tetrazolo[1,5-b]pyridazine-8-carboxylic acid, 6,7-diphenyl-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

646996-79-4

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646996-79-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 646996-79-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,6,9,9 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 646996-79:
(8*6)+(7*4)+(6*6)+(5*9)+(4*9)+(3*6)+(2*7)+(1*9)=234
234 % 10 = 4
So 646996-79-4 is a valid CAS Registry Number.

646996-79-4SDS

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 ethyl 6,7-diphenyltetrazolo[1,5-b]pyridazine-8-carboxylate

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:646996-79-4 SDS

646996-79-4Relevant academic research and scientific papers

Pyridazine derivatives and related compounds, part 9. Tetrazolo[1,5-b]pyridazine-8-carbohydrazide synthesis and some reactions

Deeb, Ali,Saad, Hosam

, p. 1873 - 1879 (2007/10/03)

The reaction of the hydrazide of 6,7-diphenyltetrazolo[1,5-b]pyridazine-8-carboxylic acid (3) with aromatic aldehydes gave 8-arylidenecarbohydrazide derivatives. The reaction of 3 with methanesulfonyl chloride, benzenesulfonyl chloride, phenyl and benzyl isothiocyanates afforded the corresponding N-substituted derivatives. The reaction of 3 with potassium ethylxanthate gave 5-(6,7-diphenyltetrazolo[1,5-blpyridazin-8-yl)-1,3,4-oxadiazole-2-thione (7). The alkylation of this product in an alkaline medium proceeds at the sulfur atom, while the aminomethylation and acylation proceed at the nitrogen atom. Compound (3) also reacted with N-aminothiosemicarbazide to give 4-amino-5-(6,7-diphenyltetrazolo[1,5-b]pyridazin-8-yl)-1,2,4-triazole-3-thione (11).

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