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1242329-23-2

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1242329-23-2 Usage

General Description

3,5-Dibromo-4-chloro-pyridin-2-ylamine is a chemical compound belonging to the class of aminopyridines. It is an organic compound with the molecular formula C5H4Br2ClN2. 3,5-DibroMo-4-chloro-pyridin-2-ylaMine is commonly used as a building block in organic synthesis, particularly in the pharmaceutical industry for the development of various medications. Its chemical structure contains two bromine atoms and one chlorine atom attached to a pyridine ring, making it a halogenated aromatic amine. 3,5-Dibromo-4-chloro-pyridin-2-ylamine is considered to be a valuable intermediate in the synthesis of various chemical compounds and is an important component in the development of pharmaceutical products.

Check Digit Verification of cas no

The CAS Registry Mumber 1242329-23-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,2,3,2 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1242329-23:
(9*1)+(8*2)+(7*4)+(6*2)+(5*3)+(4*2)+(3*9)+(2*2)+(1*3)=122
122 % 10 = 2
So 1242329-23-2 is a valid CAS Registry Number.

1242329-23-2SDS

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 3,5-dibromo-4-chloropyridin-2-amine

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:1242329-23-2 SDS

1242329-23-2Upstream product

1242329-23-2Downstream Products

1242329-23-2Relevant articles and documents

Synthesis and evaluation of the anticoccidial activity of trifluoropyrido[1,2-a]pyrimidin-2-one derivatives

Silpa, Laurence,Niepceron, Alisson,Laurent, Fabrice,Brossier, Fabien,Pénichon, Mélanie,Enguehard-Gueiffier, Cécile,Abarbri, Mohamed,Silvestre, Anne,Petrignet, Julien

supporting information, p. 114 - 120 (2015/12/18)

Screening of our chemical library to discover new molecules exhibiting in vitro activity against the invasion of host cells by Eimeria tenella revealed a lead compound with an IC50 of 15 μM. Structure-activity relationship studies were conducted with 34 newly synthesized compounds to identify more active molecules and enhance in vitro activity against the parasite. Four compounds were more effective in inhibiting MDBK cell invasion in vitro than the lead compound.

PYRIDINE DERIVATIVE

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Page/Page column 31, (2012/02/04)

The present invention relates to a novel pyridine derivative or a pharmacologically acceptable ester thereof, or a pharmacologically acceptable salt of the derivative or ester, which has an excellent hypoglycemic effect or treats and/or prevents the onset

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