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89977-04-8

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89977-04-8 Usage

Derivative of

Pyridine

Contains

Carboxylic acid group, methylamino group

Common use

Pharmaceutical research and development

Potential applications

Materials science, chemical synthesis

Subject of interest

Further study and exploration in scientific and industrial applications

Check Digit Verification of cas no

The CAS Registry Mumber 89977-04-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,9,7 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89977-04:
(7*8)+(6*9)+(5*9)+(4*7)+(3*7)+(2*0)+(1*4)=208
208 % 10 = 8
So 89977-04-8 is a valid CAS Registry Number.

89977-04-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-Pyridinedicarboxylic acid, 4-(methylamino)-

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:89977-04-8 SDS

89977-04-8Downstream Products

89977-04-8Relevant articles and documents

New synthons for the synthesis of lanthanide containing macrocyclic schiff bases featuring substituents available for tethering

Dumont, Arnaud,Jacques, Vincent,Desreux, Jean F.

, p. 2043 - 2052 (2007/10/03)

2,6-Diacetylpyridine substituted with amine or alcohol groups in the 4- position have been prepared from chelidamic acid. The key 4-chloro derivative was synthesized in high yield via a diazo intermediate and was protected as a bis-1,3-dioxane before substitution with various amino alcohol groups. Lanthanide macrocyclic tetra-imine complexes were obtained by a template procedure that leads to stable paramagnetic and/or fluorescent derivatives with anchor groups available for linkage to macromolecules. (C) 2000 Elsevier Science Ltd.

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