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5-BROMO-INDOLE-3-BUTYRIC ACID, an indole derivative, is a white solid chemical compound characterized by a molecular formula of C12H11BrNO2 and a molecular weight of 285.12 g/mol. It is recognized for its potential biological and pharmacological properties, which have made it a valuable component in research and pharmaceutical applications.

13993-31-2

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13993-31-2 Usage

Uses

Used in Pharmaceutical Research and Development:
5-BROMO-INDOLE-3-BUTYRIC ACID is used as a research compound for its potential role in the development of new therapeutic agents. Its investigation into anti-inflammatory and anti-cancer properties highlights its potential as a precursor in the synthesis of pharmaceutical compounds.
Used in Plant Biology Research:
In the field of plant biology, 5-BROMO-INDOLE-3-BUTYRIC ACID is used as a growth regulator. It is studied for its influence on plant growth and development, providing insights into the mechanisms of plant hormone action and regulation.
Used in Organic Synthesis:
5-BROMO-INDOLE-3-BUTYRIC ACID is utilized as an intermediate in organic synthesis, particularly for the production of various pharmaceutical compounds. Its unique structure and reactivity make it a key component in the synthesis of complex organic molecules with potential medicinal applications.

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 academic research and scientific papers

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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