6299-36-1 Usage
Description
(3-bromoindol-1-yl)-phenyl-methanone, with the molecular formula C15H10BrNO, is a chemical compound that is a derivative of a ketone. It features a 3-bromoindole group attached to a phenylmethanone, which contributes to its unique structure and potential biological activities.
Uses
Used in Organic Synthesis:
(3-bromoindol-1-yl)-phenyl-methanone is used as an intermediate in the synthesis of various organic compounds due to its versatile chemical properties and reactivity.
Used in Medicinal Chemistry:
(3-bromoindol-1-yl)-phenyl-methanone is used as a building block in the development of pharmaceutical compounds. Its 3-bromoindole group is known for its ability to interact with various biological targets, making it a valuable tool in drug design and discovery.
Used in Pharmaceutical Compound Preparation:
(3-bromoindol-1-yl)-phenyl-methanone is used as a key component in the preparation of pharmaceutical compounds, leveraging its unique structure to target specific biological pathways or receptors.
Used in Drug Design and Discovery:
(3-bromoindol-1-yl)-phenyl-methanone is used as a valuable tool in drug design and discovery, particularly because of the 3-bromoindole group's interaction with various biological targets, which can be exploited to create new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 6299-36-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6299-36:
(6*6)+(5*2)+(4*9)+(3*9)+(2*3)+(1*6)=121
121 % 10 = 1
So 6299-36-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H10BrNO/c16-13-10-17(14-9-5-4-8-12(13)14)15(18)11-6-2-1-3-7-11/h1-10H
6299-36-1Relevant articles and documents
REACTION OF 1-SUBSTITUTED INDOLES WITH CARBOXYLIC ACIDS AND N-IODOSUCCINIMIDE
Kwon, Sundo,Kuroki, Nobuhiko
, p. 237 - 238 (2007/10/02)
1-Substituted indoles reacted with carboxylic acids and N-iodosuccinimide to give 1-substituted-2,3-diacyloxyindolines in significant yields.