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1312581-09-1

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1312581-09-1 Usage

General Description

4-chloro-2-iodo-1-methyl-1H-pyrrolo[2,3-b]pyridine is a chemical compound with a molecular formula C8H7ClIN2. It is an organic compound with a pyrrolopyridine backbone and substituents at the 2 and 4 positions. 4-chloro-2-iodo-1-Methyl-1H-pyrrolo[2,3-b]pyridine is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It possesses potential biological activity and is of interest to researchers and pharmaceutical companies for its potential use in the development of new drugs. Additionally, it has applications in the field of organic chemistry for the synthesis of complex molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 1312581-09-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,2,5,8 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1312581-09:
(9*1)+(8*3)+(7*1)+(6*2)+(5*5)+(4*8)+(3*1)+(2*0)+(1*9)=121
121 % 10 = 1
So 1312581-09-1 is a valid CAS Registry Number.

1312581-09-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-2-iodo-1-methylpyrrolo[2,3-b]pyridine

1.2 Other means of identification

Product number -
Other names QC-4427

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:1312581-09-1 SDS

1312581-09-1Relevant articles and documents

Discovery of N-substituted 7-azaindoles as PIM1 kinase inhibitors – Part I

Barberis, Claude,Moorcroft, Neil,Arendt, Chris,Levit, Mikhail,Moreno-Mazza, Sandra,Batchelor, Joseph,Mechin, Ingrid,Majid, Tahir

, p. 4730 - 4734 (2017/09/27)

Novel N-substituted azaindoles have been discovered as PIM1 inhibitors. X-ray structures have played a significant role in orienting the chemistry effort in the initial phase of hit confirmation. Disclosure of an unconventional binding mode for 1 and 2, as demonstrated by X-ray crystallography, is presented and was an important factor in selecting and advancing a lead series.

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