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2166-25-8

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2166-25-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2166-25-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,6 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2166-25:
(6*2)+(5*1)+(4*6)+(3*6)+(2*2)+(1*5)=68
68 % 10 = 8
So 2166-25-8 is a valid CAS Registry Number.

2166-25-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 4-methylpyridazine-3,6-dicarboxylate

1.2 Other means of identification

Product number -
Other names 3,6-Bis-methoxycarbonyl-4-methyl-pyridazin

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:2166-25-8 SDS

2166-25-8Upstream product

2166-25-8Downstream Products

2166-25-8Relevant articles and documents

Study of the formation and thermal decomposition of an azo-bridged tricyclic ring system

Novak, Zoltan,Vincze, Zoltan,Czegeny, Zsuzsanna,Magyarfalvi, Gabor,Smith, David M.,Kotschy, Andras

, p. 3358 - 3363 (2007/10/03)

1-Amino-2-methyl-1,3-pentadienes were treated with dimethyl 1,2,4,5-tetrazine-3,6-dicarboxylate to give diazatricyclo[2.2.2.0]octenes and dimethyl 4-methylpyridazine-3,6-dicarboxylate, the product distribution being largely dependent on the nature of the amino substituent. Under similar conditions the analogous 1-morpholino-1,3-butadiene afforded dimethyl pyridazine-3,6-dicarboxylate as the major product. The tricyclic products underwent selective thermal decomposition to give dimethyl 4-methylpyridazine-3, 6-dicarboxylate in excellent yield. The proposed mechanism of the formation as well as of the decomposition was supported by quantum chemical calculations and experimental evidence. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.

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