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1033265-51-8

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1033265-51-8 Usage

General Description

1H-Indole-3-carboxylic acid, 5-bromo-, 1,1-dimethylethyl ester, also known as 5-Bromoindole-3-carboxylic acid, is a chemical compound with the molecular formula C14H15BrN2O2. It is a derivative of indole, which is commonly found in plants and is known for its diverse biological activities. The 5-bromo substitution on the indole ring makes this compound useful for medicinal and biochemical research, as brominated indoles have been found to possess anti-cancer, anti-inflammatory, and anti-microbial properties. The 1,1-dimethylethyl ester group adds stability and volatility to the compound, making it suitable for use in various chemical reactions and synthesis processes. Overall, 1H-Indole-3-carboxylic acid, 5-bromo-, 1,1-dimethylethyl ester is a valuable chemical building block with potential applications in pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 1033265-51-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,3,2,6 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1033265-51:
(9*1)+(8*0)+(7*3)+(6*3)+(5*2)+(4*6)+(3*5)+(2*5)+(1*1)=108
108 % 10 = 8
So 1033265-51-8 is a valid CAS Registry Number.

1033265-51-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl 5-bromo-1H-indole-3-carboxylate

1.2 Other means of identification

Product number -
Other names tert-butyl 5-bromo-1H-indole-3-carboxylate

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:1033265-51-8 SDS

1033265-51-8Downstream Products

1033265-51-8Relevant articles and documents

Palladium-catalyzed synthesis of 3-indolecarboxylic acid derivatives

Soederberg, Bjoern C. G.,Banini, Serge R.,Turner, Michael R.,Minter, Aaron R.,Arrington, Amanda K.

, p. 903 - 912 (2008/09/21)

Indoles having an ester functionality in the 3-position were prepared from 2-(2-nitrophenyl)propenoic acid derivatives via a palladium-catalyzed reductive N-heteroannulation using carbon monoxide as the ultimate reducing agent. The starting materials were

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