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1H-Pyrrolo[3,2-c]pyridine-7-carboxamide,2,3-dihydro-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84646-50-4

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84646-50-4 Usage

Molecular Structure

Pyrrolopyridine derivative

Potential Activity

Antineoplastic (cancer treatment potential)

Mechanism of Action

Selectively inhibits the WDR5-MLL interaction, disrupting the MLL complex and leading to downregulation of genes involved in leukemia cell proliferation and development

Current Status

Being studied for potential therapeutic applications in the treatment of leukemia and other types of cancer

Check Digit Verification of cas no

The CAS Registry Mumber 84646-50-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,6,4 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 84646-50:
(7*8)+(6*4)+(5*6)+(4*4)+(3*6)+(2*5)+(1*0)=154
154 % 10 = 4
So 84646-50-4 is a valid CAS Registry Number.

84646-50-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-carbamoyl-5-azaindoline

1.2 Other means of identification

Product number -
Other names 2,3-Dihydro-1H-pyrrolo[3,2-c]pyridine-7-carboxylic acid amide

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:84646-50-4 SDS

84646-50-4Downstream Products

84646-50-4Relevant academic research and scientific papers

AZAINDOLINE DERIVATIVES: 62.* SYNTHESIS AND TRANSFORMATIONS OF CONDENSED THREE-RING SYSTEMS THAT INCLUDE A 5-AZAINDOLINE FRAGMENT

Azimov, V. A.,Bychikhina, N. N.,Yakhontov, L. N.

, p. 1061 - 1064 (2007/10/02)

The reaction of 7-carbamoyl and 7-cyano-6-chloro-5-azaindolines with hydrazine leads to the formation of pyrrolopyrazolopyridine, whereas the reaction of 7-carbamoyl-5-azaindolines with dimethylformamide diethylacetal gives pyrrolopyr

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