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1H-Indole, 6-bromo-3-iodo-1-(phenylsulfonyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

180633-66-3

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180633-66-3 Usage

Derivative of indole

A heterocyclic compound commonly found in nature with diverse biological activities

Contains bromine, iodine, and a phenylsulfonyl group

These functional groups can impart specific characteristics and properties to the molecule

Potentially valuable for pharmaceutical and medicinal chemistry research

The presence of these functional groups makes it of interest for various applications in drug discovery and development

Suitable for further modification and optimization

The structure of the compound may allow for enhancements in biological activity or selectivity for particular targets

Check Digit Verification of cas no

The CAS Registry Mumber 180633-66-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,6,3 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 180633-66:
(8*1)+(7*8)+(6*0)+(5*6)+(4*3)+(3*3)+(2*6)+(1*6)=133
133 % 10 = 3
So 180633-66-3 is a valid CAS Registry Number.

180633-66-3SDS

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 1-benzenesulfonyl-6-bromo-3-iodo-1H-indole

1.2 Other means of identification

Product number -
Other names 1-Benzenesulfonyl-6-bromo-3-iodo-1H-indole

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:180633-66-3 SDS

180633-66-3Relevant academic research and scientific papers

Convenient access to bis-indole alkaloids. Application to the synthesis of?topsentins

Mal, Sajal K.,Bohé, Luis,Achab, Sa?d

, p. 5904 - 5914 (2008/12/20)

Topsentins and related bis-indole alkaloids may be efficiently synthesized through an addition/oxidation sequence leading to 2-(3-indolylcarbonyl)-imidazole derivatives followed by a Pd-catalyzed heteroarylation with the appropriate 3-stannylindoles.

Low molecular weight indole fragments as IMPDH inhibitors

Beevers, Rebekah E.,Buckley, George M.,Davies, Natasha,Fraser, Joanne L.,Galvin, Francis C.,Hannah, Duncan R.,Haughan, Alan F.,Jenkins, Kerry,Mack, Stephen R.,Pitt, William R.,Ratcliffe, Andrew J.,Richard, Marianna D.,Sabin, Verity,Sharpe, Andrew,Williams, Sophie C.

, p. 2535 - 2538 (2007/10/03)

The study of non-oxazole containing indole fragments as inhibitors of inosine monophosphate dehydrogenase (IMPDH) is described. The synthesis and in vitro inhibitory values for IMPDH II are discussed.

A three-component coupling approach to the marine bis-indole alkaloids: Topsentin, deoxytopsentin and bromotopsentin

Achab, Said

, p. 5503 - 5506 (2007/10/03)

The total syntheses of three marine bis-indole alkaloids (1, 2, 4) of the topsentin family together with the synthesis of unnatural deoxybromotopsentin (33) are described. Key elements include, a 1,2-addition-oxidation sequence to construct the bis-hetero

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