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87544-94-3

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87544-94-3 Usage

Potential biological activities

+ Slow-reacting substance of anaphylaxis (SRS-A) antagonist
+ Histamine H2-receptor antagonist
+ Potential anti-inflammatory properties
+ Potential analgesic properties
Target for further research in drug discovery and development
+ Allergy and inflammation therapies

Check Digit Verification of cas no

The CAS Registry Mumber 87544-94-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,4 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 87544-94:
(7*8)+(6*7)+(5*5)+(4*4)+(3*4)+(2*9)+(1*4)=173
173 % 10 = 3
So 87544-94-3 is a valid CAS Registry Number.

87544-94-3SDS

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-[(1-oxo-2H-pyrido[3,4-d]pyridazin-4-yl)amino]ethyl acetate

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:87544-94-3 SDS

87544-94-3Upstream product

87544-94-3Downstream Products

87544-94-3Relevant articles and documents

PYRIDAZINES CONDENSED WITH A HETERO RING, II. PYRIDO AMINOPYRIDAZINES, I. SEPARATION AND STRUCTURE DETERMINATION OF THE ISOMERIC MONOCHLORO COMPOUNDS OBTAINED BY HYDROLYSIS OF 1,4-DICHLOROPYRIDOPYRIDAZINE

Koermendy, K.,Kovacs, T.,Ruff, F.,Koevesdi, I.

, p. 487 - 500 (2007/10/02)

The separation of the mixture of isomers 2 and 3, obtained by hydrolysis of 1,4-dichloropyrido pyridazine, was accomplished and the structures of the isomers (2: 1-Cl; 3:4-Cl) were verified by synthesis.Aminolysis of 2 and 3 yielded the hydroxy-ethylamino derivatives 4 and 5; a mixture of these compounds can also be synthesized from 2-tosyloxyethylcinchomeronic imide (20 -> 4, 5) in a good yield (84percent).

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