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141102-07-0

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141102-07-0 Usage

General Description

1-propyl-1H-indole-3-carboxylic acid, also known as 3-(1-propyl-1H-indol-3-yl)propanoic acid, is a chemical compound with the molecular formula C14H15NO2. It is an indole derivative, with a propyl group attached to the 1-position of the indole ring and a carboxylic acid group at the 3-position. 1-propyl-1H-indole-3-carboxylic acid has been studied for its potential pharmaceutical properties, including as a potential anti-inflammatory and analgesic agent. It may also have potential applications in the field of medicinal chemistry for the development of novel drugs. However, further research is needed to fully understand the pharmacological and biological properties of 1-propyl-1H-indole-3-carboxylic acid.

Check Digit Verification of cas no

The CAS Registry Mumber 141102-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,1,0 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 141102-07:
(8*1)+(7*4)+(6*1)+(5*1)+(4*0)+(3*2)+(2*0)+(1*7)=60
60 % 10 = 0
So 141102-07-0 is a valid CAS Registry Number.

141102-07-0SDS

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 1-propylindole-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-propyl-1H-indole-3-carboxylic acid

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:141102-07-0 SDS

141102-07-0Downstream Products

141102-07-0Relevant articles and documents

Synthesis and biological evaluation of novel indole derivatives containing sulfonamide scaffold as potential tubulin inhibitor

Man, Ruo-Jun,Tang, Dan-Jie,Lu, Xiao-Yuan,Duan, Yong-Tao,Tao, Xiang-Xiang,Yang, Meng-Ru,Wang, Le-Le,Wang, Bao-Zhong,Xu, Chen,Zhu, Hai-Liang

, p. 1759 - 1767 (2016/09/23)

Microtubule-targeted drugs play a critical role in various types of cancer therapy worldwide. In our study, a series of novel indole derivatives containing a sulfonamide scaffold were designed, synthesized and biologically evaluated as potential tubulin p

Design, synthesis, and biological activity of potent and selective inhibitors of mast cell tryptase

Hopkins, Corey R.,Czekaj, Mark,Kaye, Steven S.,Gao, Zhongli,Pribish, James,Pauls, Henry,Liang, Guyan,Sides, Keith,Cramer, Dona,Cairns, Jennifer,Luo, Yongyi,Lim, Heng-Keang,Vaz, Roy,Rebello, Sam,Maignan, Sebastian,Dupuy, Alain,Mathieu, Magali,Levell, Julian

, p. 2734 - 2737 (2007/10/03)

A new series of novel mast cell tryptase inhibitors is reported, which features the use of an indole structure as the hydrophobic substituent on a m-benzylaminepiperidine template. The best members of this series display good in vitro activity and excellent selectivity against other serine proteases.

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