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676273-39-5

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676273-39-5 Usage

General Description

3-Iodo-1-tosyl-1h-indole-5-carbonitrile is a chemical compound also known as 5-Cyano-3-iodo-1-tosylindole. It is a heterocyclic compound with a tosyl group and a cyano group attached to an indole ring, along with a substituent of iodine. 3-Iodo-1-tosyl-1h-indole-5-carbonitrile is widely used in medicinal chemistry as a precursor for the synthesis of various biologically active molecules. It has been studied for its potential as a drug candidate in the treatment of various diseases, including cancer and neurological disorders. Its unique structural properties and reactivity make it a valuable intermediate in organic synthesis and drug discovery research.

Check Digit Verification of cas no

The CAS Registry Mumber 676273-39-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,6,2,7 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 676273-39:
(8*6)+(7*7)+(6*6)+(5*2)+(4*7)+(3*3)+(2*3)+(1*9)=195
195 % 10 = 5
So 676273-39-5 is a valid CAS Registry Number.

676273-39-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-iodo-1-tosyl-1H-indole-5-carbonitrile

1.2 Other means of identification

Product number -
Other names 3-Iodo-1-(toluene-4-sulfonyl)-1H-indole-5-carbonitrile

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:676273-39-5 SDS

676273-39-5Relevant articles and documents

H-bonding vs Protonation of Alkynes in Regioselective Hydroamination Reactions: A Glimpse into the Reactivity of Arylogous Ynolethers and Ynamines

Abe, Masahiro,Jean, Alexandre,Blanchet, Jér?me,Rouden, Jacques,Maddaluno, Jacques,De Paolis, Micha?l

, p. 15448 - 15475 (2019/11/29)

In this paper is described the competition and transition between hydrogen bonding and protonation of alkynes connected, on one side, to various aromatic rings and to chiral amino ester appendages on the other side. While the first mode of activation indu

Synthesis of a serotonin reuptake inhibitor

-

Page/Page column, (2014/09/29)

Process for the preparation of the piperazinyl derivative vilazodone, having activity as a serotonin reuptake inhibitor and used in therapy for treating serious symptoms of depression in adults, and its synthetic intermediates.

AZOLE COMPOUNDS AS PIM INHIBITORS

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, (2012/10/08)

The invention relates to bicyclic compounds of formulas I and Ia, and salts thereof. In some embodiments, the invention relates to inhibitors or modulators of Pim-1 and/or Pim-2, and/or Pim-3 protein kinase activity or enzyme function. In still further em

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