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3-Cyano-7-methylindole, also known as 3-Cyano-7-methyl-1H-indole, is a chemical compound with the molecular formula C10H8N2. It is a substituted indole derivative featuring a nitrile functional group at the 3-position and a methyl group at the 7-position of the indole ring. 3-CYANO-7-METHYLINDOLE has garnered interest due to its potential biological and pharmaceutical applications, including its role as a building block in the synthesis of various organic molecules. Additionally, it demonstrates intriguing properties as a fluorescent probe, making it a candidate for use in bioimaging studies. Its potential as a pharmaceutical intermediate in the development of new drugs targeting a range of diseases and conditions is also being explored.

194490-22-7

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194490-22-7 Usage

Uses

Used in Organic Synthesis:
3-Cyano-7-methylindole is utilized as a building block in the synthesis of various organic molecules. Its unique structure allows for the creation of a wide array of chemical entities, making it a valuable component in organic chemistry.
Used as a Fluorescent Probe in Bioimaging Studies:
3-CYANO-7-METHYLINDOLE serves as a fluorescent probe due to its interesting optical properties. It is used in bioimaging studies to visualize and track specific biological processes or structures within living organisms, contributing to advancements in life sciences research.
Used in Pharmaceutical Development:
3-Cyano-7-methylindole is recognized for its potential as a pharmaceutical intermediate. It plays a crucial role in the development of new drugs that target a variety of diseases and conditions, showcasing its versatility and importance in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 194490-22-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,4,9 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 194490-22:
(8*1)+(7*9)+(6*4)+(5*4)+(4*9)+(3*0)+(2*2)+(1*2)=157
157 % 10 = 7
So 194490-22-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H8N2/c1-7-3-2-4-9-8(5-11)6-12-10(7)9/h2-4,6,12H,1H3

194490-22-7SDS

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 7-methyl-1H-indole-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 1H-Indole-3-carbonitrile,7-methyl

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:194490-22-7 SDS

194490-22-7Downstream Products

194490-22-7Relevant academic research and scientific papers

GaCl3-Catalyzed C-H Cyanation of Indoles with N-Cyanosuccinimide

Wang, Xue,Makha, Mohamed,Chen, Shu-Wei,Zheng, Huaiji,Li, Yuehui

, p. 6199 - 6206 (2019/05/24)

An efficient GaCl3-catalyzed direct cyanation of indoles and pyrroles using bench-stable electrophilic cyanating agent N-cyanosuccinimide was achieved and afforded 3-cyanoindoles and 2-cyanopyrroles in good yields and excellent regioselectivities. Notably, this protocol exhibited high reactivity for unprotected indoles and was applicable to a broad range of indole and pyrrole substrates.

NITROGENATED HETEROCYCLIC COMPOUND AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME

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Page/Page column 15; 21, (2008/12/06)

The present invention relates to novel compounds having a xanthine oxidase inhibitory effect and an uricosuric effect and pharmaceutical compositions comprising the same as an active ingredient. That is, the present invention relates nitrogen-containing heterocyclic compounds represented by the following general formula (I): wherein Y1 represents N or C(R4) ; Y2 represents N or C(R5) ; R4 and R5 independently represent an alkyl group, a hydrogen atom etc. ; one of R1 and R2 represents an optionally substituted aryl group, an alkoxygroup or an optionally substituted heterocyclic group; the other of R1 and R2 represents a haloalkyl group, a cyanogroup, ahalogenatometc.; and R3 represents a 5-tetrazolyl group or a carboxy group, and pharmaceutically acceptable salts thereof, and pharmaceutical compositions comprising the same as an active ingredient.

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