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180623-97-6

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180623-97-6 Usage

Derivative of indole

A heterocyclic organic compound commonly found in natural products and pharmaceuticals

Iodine atoms

Two atoms located at positions 2 and 3 in the indole ring

Potential applications

Organic synthesis, medicinal chemistry, and materials science

Unique properties

May be useful for research and development in chemistry and related disciplines

Structural features

The presence of two iodine atoms in the indole ring gives this compound its unique properties and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 180623-97-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,6,2 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 180623-97:
(8*1)+(7*8)+(6*0)+(5*6)+(4*2)+(3*3)+(2*9)+(1*7)=136
136 % 10 = 6
So 180623-97-6 is a valid CAS Registry Number.

180623-97-6SDS

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 2,3-diiodo-1-methylindole

1.2 Other means of identification

Product number -
Other names N-methyl-2,3-diiodoindole

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:180623-97-6 SDS

180623-97-6Relevant articles and documents

Decarboxylative Halogenation and Cyanation of Electron-Deficient Aryl Carboxylic Acids via Cu Mediator as Well as Electron-Rich Ones through Pd Catalyst under Aerobic Conditions

Fu, Zhengjiang,Li, Zhaojie,Song, Yuanyuan,Yang, Ruchun,Liu, Yanzhu,Cai, Hu

, p. 2794 - 2803 (2016/04/26)

Simple strategies for decarboxylative functionalizations of electron-deficient benzoic acids via using Cu(I) as promoter and electron-rich ones by employing Pd(II) as catalyst under aerobic conditions have been established, which lead to smooth synthesis of aryl halides (-I, Br, and Cl) through the decarboxylative functionalization of benzoic acids with readily available halogen sources CuX (X = I, Br, Cl), and easy preparation of benzonitriles from decarboxylative cyanation of aryl carboxylic acids with nontoxic and low-cost K4Fe(CN)6 under an oxygen atmosphere for the first time.

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