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55275-98-4

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55275-98-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55275-98-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,7 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 55275-98:
(7*5)+(6*5)+(5*2)+(4*7)+(3*5)+(2*9)+(1*8)=144
144 % 10 = 4
So 55275-98-4 is a valid CAS Registry Number.

55275-98-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dimethyl-3-N,5-N-diphenylpyridine-3,5-dicarboxamide

1.2 Other means of identification

Product number -
Other names 3,5-bis[N-(phenyl)carbamoyl]-2,6-dimethylpyridine

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:55275-98-4 SDS

55275-98-4Downstream Products

55275-98-4Relevant articles and documents

Convenient synthesis of 3,5-biscarbamoyl-pyridine derivatives

Wang, Xiayun,Zhu, Yiwen,Zhang, Min,Lu, Dongliang,Qian, Qun,Chen, Yali,Cao, Weiguo,Song, Liping,Deng, Hongmei

, p. 2119 - 2123 (2012/03/11)

An efficient and convenient method for synthesis of 3,5-bis-carbamoyl-2,6- dimethylpyridine derivatives was achieved in good to excellent yields by reaction of anilines with 3,5-bis(3',5'-dimethyl-1'-pyrazolyl-carbonyl)-2,6- dimethylpyridine, in which pyr

Reductions with NADH Models. 3. The High Reactivity of Hantzsch Amides

Gelbard, Georges,Lin, Jian,Roques, Nathalie

, p. 1789 - 1793 (2007/10/02)

Aromatic ketones and aldehydes are rapidly reduced by various 1,4-dihydropyridines, several of which can be considered to be a model of NADH.The reducing agents bear amide groups and are closely related to Hantzsch esters.They exhibit the highest reactivity among NADH models so far described.In some cases, the rate and completeness of reduction by Hantzsch amides compare favorably with those of reduction by the usually employed metal hydrides.

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