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Ethyl 5-bromo-1H-indole-7-carboxylate is a chemical compound belonging to the indole family, characterized by the molecular formula C12H10BrNO2. It features a bromo group and an ethyl ester functional group, which contribute to its unique structure and reactivity. Ethyl 5-broMo-1H-indole-7-carboxylate is recognized for its potential bioactivity and pharmacological properties, making it a valuable intermediate in the synthesis of various pharmaceuticals and bioactive molecules.

1065181-58-9

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1065181-58-9 Usage

Uses

Used in Organic Synthesis:
Ethyl 5-bromo-1H-indole-7-carboxylate is used as a building block in organic synthesis for the creation of diverse chemical compounds. Its structure and reactivity make it a versatile intermediate, facilitating the production of a wide range of molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Ethyl 5-bromo-1H-indole-7-carboxylate is utilized as a key intermediate for the synthesis of pharmaceuticals. Its presence in the indole ring suggests potential bioactivity, which is of interest for drug discovery and development, as it may contribute to the creation of new therapeutic agents.
Used in Drug Discovery and Development:
Ethyl 5-bromo-1H-indole-7-carboxylate is employed as a target for research in drug discovery and development due to its potential pharmacological properties. Ethyl 5-broMo-1H-indole-7-carboxylate's structure and functional groups make it a promising candidate for the exploration of new therapeutic applications and the advancement of existing treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 1065181-58-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,5,1,8 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1065181-58:
(9*1)+(8*0)+(7*6)+(6*5)+(5*1)+(4*8)+(3*1)+(2*5)+(1*8)=139
139 % 10 = 9
So 1065181-58-9 is a valid CAS Registry Number.

1065181-58-9SDS

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 Ethyl 5-bromo-1H-indole-7-carboxylate

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 -
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More Details:1065181-58-9 SDS

1065181-58-9Relevant academic research and scientific papers

3,5-Disubstituted-indole-7-carboxamides as IKKβ Inhibitors: Optimization of Oral Activity via the C3 Substituent

Kerns, Jeffrey K.,Busch-Petersen, Jakob,Fu, Wei,Boehm, Jeffrey C.,Nie, Hong,Muratore, Michael,Bullion, Ann,Lin, Guoliang,Li, Huijie,Davis, Roderick,Lin, Xichen,Lakdawala, Ami S.,Cousins, Rick,Field, Rita,Payne, Jeremy,Miller, David D.,Bamborough, Paul,Christopher, John A.,Baldwin, Ian,Osborn, Ruth R.,Yonchuk, John,Webb, Edward,Rumsey, William L.

, p. 1164 - 1169 (2018/11/23)

IκB kinase β (IKKβ or IKK2) is a key regulator of nuclear factor kappa B (NF-κB) and has received attention as a therapeutic target. Herein we report on the optimization of a series of 3,5-disubstituted-indole-7-carboxamides for oral activity. In doing so

INDOLE CARBOXAMIDES AS IKK2 INHIBITORS

-

, (2008/12/04)

The invention is directed to novel indole carboxamide compounds. Specifically, the invention is directed to compounds according to formula (I): wherein R1, R2, R3, R4, and m are as defined herein. The compounds of the invention are inhibitors of IKK2 and can be useful in the treatment of disorders associated with inappropriate IKK2 (also known as IKKβ) activity, such as rheumatoid arthritis, asthma, rhinitis, and COPD (chronic obstructive pulmonary disease). Accordingly, the invention is further directed to pharmaceutical compositions comprising a compound of the invention. The invention is still further directed to methods of inhibiting IKK2 activity and treatment of disorders associated therewith using a compound of the invention or a pharmaceutical composition comprising a compound of the invention.

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