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3-Iodo-1-tosyl-1H-indole-5-carbonitrile, also known as 5-Cyano-3-iodo-1-tosylindole, is a heterocyclic chemical compound characterized by the presence of a tosyl group and a cyano group attached to an indole ring, along with an iodine substituent. 3-Iodo-1-tosyl-1h-indole-5-carbonitrile is recognized for its unique structural properties and reactivity, making it a valuable intermediate in the fields of organic synthesis and drug discovery research.

676273-39-5

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676273-39-5 Usage

Uses

Used in Medicinal Chemistry:
3-Iodo-1-tosyl-1H-indole-5-carbonitrile is utilized as a precursor in the synthesis of various biologically active molecules, playing a crucial role in the development of new pharmaceuticals.
Used in Drug Synthesis:
In the pharmaceutical industry, 3-Iodo-1-tosyl-1H-indole-5-carbonitrile is employed as a key intermediate for the creation of potential drug candidates aimed at treating a range of diseases, including cancer and neurological disorders.
Used in Organic Synthesis Research:
3-Iodo-1-tosyl-1H-indole-5-carbonitrile serves as a versatile building block in organic synthesis, facilitating the development of complex molecular structures and contributing to the advancement of chemical science.
3-Iodo-1-tosyl-1h-indole-5-carbonitrile's potential as a drug candidate is attributed to its unique structural features, which allow for targeted interactions with biological targets, thus offering therapeutic benefits in various medical conditions.

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 academic research and scientific papers

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

HETEROARYL COMPOUNDS AS AGROCHEMICAL FUNGICIDES

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Page/Page column 162, (2018/12/13)

Heteroaryl compounds as agrochemical fungicides Formula (I) The present invention relates to heteroaryl compounds of formula (I) or a compound in the form of a stereoisomer, an agriculturally acceptable salt, a tautomer, an isotopic form, a N-oxide, a S- oxide, a prodrug or mixture thereof. The present invention further relates to the use of a com- pound of formula (I). Furthermore, the present invention relates to methods for combating phy- topathogenic harmful fungi, which methods comprising the steps of treatment of the phytopatho- genic fungi, the plant orthe plant propagation material selected from seeds, roots, fruits, tubers, bulbs, rhizomes, shoots, sprouts and other parts of plants, including seedlings and young plants to be protected against fungal attack, stored materials or harvest, or alternatelythe locus or soil or soil substituents or surfaces therefrom, with at least one compound of formula (I).

SYNTHESIS OF A SEROTONIN REUPTAKE INHIBITOR

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Paragraph 0062; 0063, (2014/09/30)

Process for the preparation of a piperazinyl derivative, and its intermediates, which has known activity as a serotonin reuptake inhibitor and is used in therapy for treating serious symptoms of depression in adults.

Synthesis of a serotonin reuptake inhibitor

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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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Page/Page column 193, (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

Conformationally restricted homotryptamines. Part 5: 3-(trans-2-aminomethylcyclopentyl)indoles as potent selective serotonin reuptake inhibitors

Denhart, Derek J.,Deskus, Jeffrey A.,Ditta, Jonathan L.,Gao, Qi,Dalton King,Kozlowski, Edward S.,Meng, Zhaoxing,LaPaglia, Melissa A.,Mattson, Gail K.,Molski, Thaddeus F.,Taber, Matthew T.,Lodge, Nicholas J.,Mattson, Ronald J.,Macor, John E.

scheme or table, p. 4031 - 4033 (2010/03/05)

A series of racemic 3-(trans-2-aminomethylcyclopentyl)indoles was synthesized and found to have potent binding to the human serotonin transporter (hSERT). The most active analog was synthesized stereospecifically and the active enantiomer was shown to hav

Compounds for the treatment of premature ejaculation

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Page/Page column 9, (2010/11/30)

The present invention relates to compounds of Formula (I) and pharmaceutically acceptable salts or solvates thereof and pharmaceutically acceptable formulations comprising said compounds useful for the treatment of premature ejaculation, depression, atten

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