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1160112-78-6

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1160112-78-6 Usage

General Description

2H-Pyrrolo[2,3-b]pyridin-2-one, 1,3-dihydro-5-iodo- is a chemical compound with the molecular formula C8H7INO. It is a heterocyclic compound with a pyrrolopyridine core and a dihydro-2-one structure. 2H-Pyrrolo[2,3-b]pyridin-2-one,1,3-dihydro-5-iodo- is commonly used as a building block in the synthesis of pharmaceuticals and other organic compounds. The presence of the iodine atom in the molecule gives it unique properties and makes it valuable for use in organic chemistry reactions. Additionally, it has the potential to exhibit biological activity, making it of interest in medicinal chemistry research.

Check Digit Verification of cas no

The CAS Registry Mumber 1160112-78-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,0,1,1 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1160112-78:
(9*1)+(8*1)+(7*6)+(6*0)+(5*1)+(4*1)+(3*2)+(2*7)+(1*8)=96
96 % 10 = 6
So 1160112-78-6 is a valid CAS Registry Number.

1160112-78-6SDS

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 5-iodo-1,3-dihydropyrrolo[2,3-b]pyridin-2-one

1.2 Other means of identification

Product number -
Other names 5-iodo-1H-pyrrolo[2,3-b]pyridin-2(3H)-one

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:1160112-78-6 SDS

1160112-78-6Downstream Products

1160112-78-6Relevant articles and documents

Synthesis, kinase inhibitory potencies and in vitro antiproliferative activity of isoindigo and 7′-azaisoindigo derivatives substituted by Sonogashira cross-coupling

Bouchikhi, Fadoua,Anizon, Fabrice,Moreau, Pascale

experimental part, p. 2705 - 2710 (2009/10/02)

In the course of structure-activity relationship studies we were interested in the synthesis of isoindigo and 7′-azaisoindigo derivatives substituted at the N-1 position by a 1-(2,3,4,6-tetra-O-acetyl-β-d-glucopyranosyl), at the 5′-position by various cha

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