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1H-Indole, 2,3-dihydro-1-[(2-iodophenyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138154-63-9

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138154-63-9 Usage

Molecular structure

A 2,3-dihydro-1H-indole core with an iodophenylmethyl substituent attached

Derivative of

Tryptophan (an amino acid)

Primary use

Research and drug development

Potential biological activity

Being studied for its potential use in the treatment of various diseases, including cancer and neurological disorders

Use as a precursor

In the synthesis of other pharmaceutical compounds

Unique property

As an iodinated indole derivative, it has the potential to interact with biological systems in unique ways

Value in research

It is a valuable tool for studying the molecular mechanisms of disease and for the development of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 138154-63-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,1,5 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 138154-63:
(8*1)+(7*3)+(6*8)+(5*1)+(4*5)+(3*4)+(2*6)+(1*3)=129
129 % 10 = 9
So 138154-63-9 is a valid CAS Registry Number.

138154-63-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(2-iodophenyl)methyl]-2,3-dihydroindole

1.2 Other means of identification

Product number -
Other names 1-(2-iodobenzyl)indoline

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:138154-63-9 SDS

138154-63-9Relevant academic research and scientific papers

Samarium Diiodide Mediated Alkylation of Saturated Heterocycles alpha to Nitrogen

Booth, Susan E.,Benneche, Tore,Undheim, Kjell

, p. 3665 - 3674 (2007/10/02)

A method for α-alkylation of saturated 5-, 6-, 7- and 8-membered aza-heterocycles is described.The auxiliary is an o-iodobenzyl group attached at the nitrogen.A radical introduced in the o-position is transferred to the amine α-position which subsequently leads to an addition reaction with pentan-3-one.

Generation and Alkylation of Carbanions α to the Nitrogen of Amines by a New Metalation Procedure

Murakami, Masahiro,Hayashi, Minoru,Ito, Yoshihiko

, p. 793 - 794 (2007/10/02)

Treatment of a tertiary amine having a pendent o-iodobenzyl group on nitrogen with SmI2 generates α-amino organosamarium, which reacts with electrophiles giving the corresponding C-C bond formation products in good yield.

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