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65880-18-4

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65880-18-4 Usage

General Description

Ethyl 4,5,6,7-tetrahydro-1H-indole-2-carboxylate is a chemical compound with the molecular formula C13H17NO2. It is an ester of indole-2-carboxylic acid and ethyl alcohol. ethyl 4,5,6,7-tetrahydro-1H-indole-2-carboxylate is commonly used as a precursor in the synthesis of various pharmaceuticals and industrial chemicals. It exhibits biological activity and has been studied for its potential therapeutic applications, particularly in the field of medicinal chemistry. The compound is also of interest in the development of new materials and research in the field of organic chemistry. Overall, ethyl 4,5,6,7-tetrahydro-1H-indole-2-carboxylate has a range of potential uses and applications in various scientific and industrial disciplines.

Check Digit Verification of cas no

The CAS Registry Mumber 65880-18-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,8,8 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 65880-18:
(7*6)+(6*5)+(5*8)+(4*8)+(3*0)+(2*1)+(1*8)=154
154 % 10 = 4
So 65880-18-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO2/c1-2-14-11(13)10-7-8-5-3-4-6-9(8)12-10/h7,12H,2-6H2,1H3

65880-18-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4,5,6,7-tetrahydro-1H-indole-2-carboxylate

1.2 Other means of identification

Product number -
Other names 4,5,6,7-Tetrahydro-indol-2-carbonsaeure-aethylester

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:65880-18-4 SDS

65880-18-4Downstream Products

65880-18-4Relevant articles and documents

Discovery of Potent and Selective Tricyclic Inhibitors of Bruton's Tyrosine Kinase with Improved Druglike Properties

Wang, Xiaojing,Barbosa, James,Blomgren, Peter,Bremer, Meire C.,Chen, Jacob,Crawford, James J.,Deng, Wei,Dong, Liming,Eigenbrot, Charles,Gallion, Steve,Hau, Jonathon,Hu, Huiyong,Johnson, Adam R.,Katewa, Arna,Kropf, Jeffrey E.,Lee, Seung H.,Liu, Lichuan,Lubach, Joseph W.,Macaluso, Jen,Maciejewski, Pat,Mitchell, Scott A.,Ortwine, Daniel F.,Dipaolo, Julie,Reif, Karin,Scheerens, Heleen,Schmitt, Aaron,Wong, Harvey,Xiong, Jin-Ming,Xu, Jianjun,Zhao, Zhongdong,Zhou, Fusheng,Currie, Kevin S.,Young, Wendy B.

supporting information, p. 608 - 613 (2017/06/13)

In our continued effort to discover and develop best-in-class Bruton's tyrosine kinase (Btk) inhibitors for the treatment of B-cell lymphomas, rheumatoid arthritis, and systemic lupus erythematosus, we devised a series of novel tricyclic compounds that improved upon the druglike properties of our previous chemical matter. Compounds exemplified by G-744 are highly potent, selective for Btk, metabolically stable, well tolerated, and efficacious in an animal model of arthritis.

HETEROARYL PYRIDONE AND AZA-PYRIDONE AMIDE COMPOUNDS

-

, (2015/01/16)

Heteroaryl pyridone and aza-pyridone amide compounds of Formula (I) are provided, and various substituents including stereoisomers, tautomers, and pharmaceutically acceptable salts thereof, useful for inhibiting Btk, and for treating cancer and immune disorders such as inflammation mediated by Btk. Methods of using compounds of Formula I for in vitro, in situ, and in vivo diagnosis, and treatment of such disorders in mammalian cells, or associated pathological conditions, are disclosed.

ALKYLATED PIPERAZINE COMPOUNDS

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Paragraph 0406; 0407, (2013/05/21)

Alkylated piperazine compounds of Formula I are provided, including stereoisomers, tautomers, and pharmaceutically acceptable salts thereof, useful for inhibiting Btk kinase, and for treating immune disorders such as inflammation mediated by Btk kinase. Methods of using compounds of Formula I for in vitro, in situ, and in vivo diagnosis, and treatment of such disorders in mammalian cells, or associated pathological conditions, are disclosed.

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