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80360-26-5 Usage

Chemical class

Indole derivatives

Characteristic features

Two iodine atoms, a phenylsulfonyl group attached to the indole ring

Potential applications

Organic chemistry, pharmaceuticals

Unique attributes

Structural features, reactivity

Usage

Building block for synthesis of organic molecules, possible biological activity

Relevance

Interest for drug discovery and development, valuable tool for chemical research and synthesis processes

Check Digit Verification of cas no

The CAS Registry Mumber 80360-26-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,3,6 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 80360-26:
(7*8)+(6*0)+(5*3)+(4*6)+(3*0)+(2*2)+(1*6)=105
105 % 10 = 5
So 80360-26-5 is a valid CAS Registry Number.

80360-26-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	1-(benzenesulfonyl)-2,3-diiodoindole

1.2 Other means of identification

Product number	-
Other names	2,3-diiodo-1-phenylsulfonylindole

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:80360-26-5 SDS

80360-26-5Upstream product

80360-26-5Downstream Products

80360-26-5Relevant articles and documents

Decarboxylative halogenation of indolecarboxylic acids using hypervalent iodine(III) reagent and its application to the synthesis of polybromoindoles

Hamamoto, Hiromi,Umemoto, Hideaki,Umemoto, Misako,Ohta, Chiaki,Fujita, Emi,Nakamura, Akira,Maegawa, Tomohiro,Miki, Yasuyoshi

, p. 561 - 572 (2015/05/20)

Hypervalent iodine mediated decarboxylative halogenation of indoledicarboxylic acid derivatives was studied. The treatment of 1-methylindole-2,3-dicarboxylic acid with phenyliodine diacetate (PIDA) in the presence of lithium bromide gave 1-methyl-3,3-brom

Hypervalent iodine(III) mediated decarboxylative halogenation of indolecarboxylic acids for the synthesis of haloindole derivatives

Hamamoto, Hiromi,Umemoto, Hideaki,Umemoto, Misako,Ohta, Chiaki,Dohshita, Masashi,Miki, Yasuyoshi

scheme or table, p. 2593 - 2596 (2010/11/24)

The treatment of 1-methylindole-2,3-dicarboxylic acid with hypervalent iodine(III) reagent, phenyliodine diacetate (PIDA), in the presence of lithium bromide gave 1-methyl-3,3-dibromooxindole. However, the reaction of 1-(phenylsulfonyl)indole-2,3-dicarboxylic acid with PIDA in the presence of lithium bromide afforded 2,3-dibromo-1-(phenylsulfonyl)indole. In a similar manner, the 2,3-dichloro- and 2,3-diiodo-indole derivatives were obtained by the reaction of the indole-2,3-dicarboxylic acids with PIDA in the presence of lithium chloride and iodide. Georg Thieme Verlag Stuttgart New York.

Efficient Synthesis of 2-Chloro-, 2-Bromo-, and 2-Iodoindole

Bergman, Jan,Venemalm, Lennart

, p. 2495 - 2497 (2007/10/02)

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CAS

80360-26-5