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1H-Pyrrolo[2,3-c]pyridine, 7-bromo-5-chlorois a chemical compound with a unique heterocyclic structure characterized by a pyrrolopyridine ring system. It is distinguished by the presence of a bromine atom at the 7th position and a chlorine atom at the 5th position on the aromatic ring. 1H-Pyrrolo[2,3-c]pyridine, 7-bromo-5-chlorois of interest in the field of medicinal chemistry and drug discovery due to its potential pharmacological properties.

945840-69-7

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945840-69-7 Usage

Uses

Used in Pharmaceutical Development:
1H-Pyrrolo[2,3-c]pyridine, 7-bromo-5-chlorois used as a potential pharmaceutical agent for the development of novel therapeutics. Its unique structure and potential pharmacological properties make it a promising candidate for various therapeutic indications.
Used in Organic Synthesis:
1H-Pyrrolo[2,3-c]pyridine, 7-bromo-5-chlorois used as a building block in organic synthesis for the creation of diverse molecular structures with potential biological activities. Its unique heterocyclic structure allows for the development of new compounds with potential applications in various fields.
Further research and investigation into the properties and potential applications of 1H-Pyrrolo[2,3-c]pyridine, 7-bromo-5-chloroare warranted to fully understand its scientific and commercial potential.

Check Digit Verification of cas no

The CAS Registry Mumber 945840-69-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,8,4 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 945840-69:
(8*9)+(7*4)+(6*5)+(5*8)+(4*4)+(3*0)+(2*6)+(1*9)=207
207 % 10 = 7
So 945840-69-7 is a valid CAS Registry Number.

945840-69-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Pyrrolo[2,3-c]pyridine, 7-bromo-5-chloro-

1.2 Other means of identification

Product number -
Other names 7-Bromo-5-chloro-1H-pyrrolo[2,3-c]pyridine

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:945840-69-7 SDS

945840-69-7Downstream Products

945840-69-7Relevant academic research and scientific papers

A Unique Approach to Design Potent and Selective Cyclic Adenosine Monophosphate Response Element Binding Protein, Binding Protein (CBP) Inhibitors

Bronner, Sarah M.,Murray, Jeremy,Romero, F. Anthony,Lai, Kwong Wah,Tsui, Vickie,Cyr, Patrick,Beresini, Maureen H.,De Leon Boenig, Gladys,Chen, Zhongguo,Choo, Edna F.,Clark, Kevin R.,Crawford, Terry D.,Jayaram, Hariharan,Kaufman, Susan,Li, Ruina,Li, Yingjie,Liao, Jiangpeng,Liang, Xiaorong,Liu, Wenfeng,Ly, Justin,Maher, Jonathan,Wai, John,Wang, Fei,Zheng, Aijun,Zhu, Xiaoyu,Magnuson, Steven

, p. 10151 - 10171 (2018/01/10)

The epigenetic regulator CBP/P300 presents a novel therapeutic target for oncology. Previously, we disclosed the development of potent and selective CBP bromodomain inhibitors by first identifying pharmacophores that bind the KAc region and then building into the LPF shelf. Herein, we report the "hybridization" of a variety of KAc-binding fragments with a tetrahydroquinoline scaffold that makes optimal interactions with the LPF shelf, imparting enhanced potency and selectivity to the hybridized ligand. To demonstrate the utility of our hybridization approach, two analogues containing unique Asn binders and the optimized tetrahydroquinoline moiety were rapidly optimized to yield single-digit nanomolar inhibitors of CBP with exquisite selectivity over BRD4(1) and the broader bromodomain family.

ALKYNYL ALCOHOLS AND METHODS OF USE

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Paragraph 0577; 0578, (2015/03/04)

The invention relates to compounds of Formula (0): wherein A1-A8, R4 and R5 each has the meaning as described herein. Compounds of Formula (0) and pharmaceutical compositions thereof are useful in the treatment of diseases and disorders in which undesired or over-activation of NF-kB signaling is observed.

ALKYNYL ALCOHOLS AND METHODS OF USE

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Page/Page column 142; 143, (2015/03/13)

The invention relates to compounds of Formula (0): wherein A1-A8, R4 and R5 each has the meaning as described herein. Compounds of Formula (0) and pharmaceutical compositions thereof are useful in the treatment of diseases and disorders in which undesired or over-activation of NF-kB signaling is observed.

Heterobicyclic amide compounds

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Page/Page column 9, (2010/11/28)

Compounds of formula I processes for their preparation and pharmaceutical compositions comprising them.

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