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13993-31-2

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13993-31-2 Usage

General Description

5-Bromo-indole-3-butyric acid is a chemical compound that belongs to the class of indole derivatives. It is a white solid with a molecular formula of C12H11BrNO2 and a molecular weight of 285.12 g/mol. 5-BROMO-INDOLE-3-BUTYRIC ACID is often used in research and pharmaceutical applications due to its potential biological and pharmacological properties. It has been studied for its potential role as a growth regulator in plants and as an intermediate in the synthesis of various pharmaceutical compounds. 5-Bromo-indole-3-butyric acid has also been investigated for its potential anti-inflammatory and anti-cancer properties, making it a subject of interest in the development of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 13993-31-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,9 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13993-31:
(7*1)+(6*3)+(5*9)+(4*9)+(3*3)+(2*3)+(1*1)=122
122 % 10 = 2
So 13993-31-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H12BrNO2/c13-9-4-5-11-10(6-9)8(7-14-11)2-1-3-12(15)16/h4-7,14H,1-3H2,(H,15,16)

13993-31-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(5-bromo-1H-indol-3-yl)butanoic acid

1.2 Other means of identification

Product number -
Other names 4-(5-bromo-indol-3-yl)-butyric 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:13993-31-2 SDS

13993-31-2Downstream Products

13993-31-2Relevant articles and documents

Deciphering DNA-based asymmetric catalysis through intramolecular Friedel-Crafts alkylations

Park, Soyoung,Ikehata, Keiichi,Watabe, Ryo,Hidaka, Yuta,Rajendran, Arivazhagan,Sugiyama, Hiroshi

, p. 10398 - 10400,3 (2020/09/09)

We describe asymmetric intramolecular Friedel-Crafts alkylations with a DNA-based hybrid catalyst and propose a plausible binding model. This study shows promise for studying relationships between the helical chirality of DNA and enantioselectivity of the chemical reaction.

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