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126921-19-5

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126921-19-5 Usage

Description

1H-Indole-3-carbonylchloride, 1-methylis an organic compound that serves as a key intermediate in the synthesis of various pharmaceuticals and organic compounds. It is characterized by its indole ring structure with a carbonyl chloride group attached to the 3-position and a methyl group at the 1-position. This unique structure endows it with reactivity and properties that make it a valuable building block in organic synthesis.
Used in Pharmaceutical Industry:
1H-Indole-3-carbonylchloride, 1-methylis used as a reactant for the preparation of indolo[2,3-a]pyrimido[5,4-c]carbazole derivatives, which are of significant interest due to their potential as anti-cancer agents. The incorporation of this compound into the synthesis process allows for the development of novel and more effective cancer treatments, targeting specific molecular pathways and mechanisms involved in tumor growth and progression.

Check Digit Verification of cas no

The CAS Registry Mumber 126921-19-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,9,2 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 126921-19:
(8*1)+(7*2)+(6*6)+(5*9)+(4*2)+(3*1)+(2*1)+(1*9)=125
125 % 10 = 5
So 126921-19-5 is a valid CAS Registry Number.

126921-19-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methylindole-3-carbonyl chloride

1.2 Other means of identification

Product number -
Other names 1H-Indole-3-carbonylchloride,1-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:126921-19-5 SDS

126921-19-5Relevant articles and documents

Prodrug compound and application thereof in treatment of cancer

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Paragraph 0135-0136, (2021/03/06)

The present invention provides a compound indicated by a formula (I), pharmaceutically acceptable salts or esters thereof, a pharmaceutical composition of the compound, and the use of the compound andthe pharmaceutical composition in inhibition or regulation of tyrosine kinase activity, and treatment of tyrosine kinase mediated disease symptoms or disorders including cancer.

Palladium-Catalyzed Tandem Dehydrogenative [4 + 2] Annulation of Terminal Olefins with N-Sulfonyl Amides via C-H Activations

Sun, Manman,Chen, Weida,Xia, Xiangyu,Shen, Guodong,Ma, Yongmin,Yang, Jianguo,Ding, Hanfeng,Wang, Zhiming

supporting information, p. 3229 - 3233 (2020/04/10)

A palladium-catalyzed tandem dehydrogenative [4 + 2] annulation of terminal olefins with N-sulfonyl amides via C(sp2)-H activation, allylic C(sp3)-H activation, and homoallylic C(sp3)-H elimination processes has been developed. Promoted by the DMSO ligand, various benzamides, heterocyclic arylamides, alkenyl carboxamides, and commercial olefins are found to be efficient substrates to construct important heterocyclic compounds bearing a vinyl substituent with high E stereoselectivity. Using air as the terminal oxidant also provides a great advantage regarding environmental friendliness.

Preparation method for synthesizing spiro indolone based on furan and indole aryloxy bifunctionalization and application thereof

-

Paragraph 0021, (2020/05/05)

The invention discloses a preparation method for synthesizing spiro indolone based on furan and indole aryloxy bifunctionalization. An indole derivative (N-(o-bromophenyl)-3-indole formamide) which issimple and easy to synthesize is used for regioselectiv

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