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14229-27-7

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14229-27-7 Usage

General Description

3-amino-5,6-dichloropyrazine-2-carboxamide is a chemical compound with the molecular formula C5H4Cl2N4O. It is a pyrazine derivative that contains an amino group and two chlorine atoms. 3-amino-5,6-dichloropyrazine-2-carboxamide has various applications in the pharmaceutical and agricultural industries, including serving as an intermediate in the synthesis of pharmaceutical drugs and in the development of new agrochemicals. Additionally, it can also be used as a building block in organic synthesis and in the study of chemical reactions and mechanisms. Its properties and structure make it a valuable component in various research and industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 14229-27-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,2 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14229-27:
(7*1)+(6*4)+(5*2)+(4*2)+(3*9)+(2*2)+(1*7)=87
87 % 10 = 7
So 14229-27-7 is a valid CAS Registry Number.

14229-27-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Amino-5,6-dichloropyrazine-2-carboxamide

1.2 Other means of identification

Product number -
Other names 3-amino-5,6-dichloropyrazine-2-carboxamide

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:14229-27-7 SDS

14229-27-7Relevant articles and documents

2-Amidino analogs of glycine-amiloride conjugates: Inhibitors of urokinase-type plasminogen activator

Massey, Archna P.,Harley, William R.,Pasupuleti, Nagarekha,Gorin, Fredric A.,Nantz, Michael H.

supporting information; experimental part, p. 2635 - 2639 (2012/05/20)

The relative non-toxicity of the diuretic amiloride, coupled with its selective inhibition of the protease urokinase plasminogen activator (uPA), makes this compound class attractive for structure-activity studies. Herein we substituted the C(2)-acylguani

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