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METHYL 3-AMINO-4-CHLORO-1-BENZOTHIOPHENE-2-CARBOXYLATE is a synthetic chemical compound with the molecular formula C11H8ClNO2S. It features a benzothiophene ring with a chlorine substituent and a carboxylate group attached to the second carbon atom. METHYL 3-AMINO-4-CHLORO-1-BENZOTHIOPHENE-2-CARBOXYLATE is commonly used as a building block in organic chemistry for the creation of more complex molecules and serves as a synthetic intermediate in the production of pharmaceuticals and agrochemicals. Its potential applications in medicinal chemistry and drug development make it a valuable component in the field of chemical research.

35212-86-3

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35212-86-3 Usage

Uses

Used in Pharmaceutical Industry:
METHYL 3-AMINO-4-CHLORO-1-BENZOTHIOPHENE-2-CARBOXYLATE is used as a synthetic intermediate for the development of various pharmaceuticals. Its unique structure allows for the creation of complex molecules with potential therapeutic properties, contributing to the advancement of new drug discoveries.
Used in Agrochemical Industry:
In the agrochemical sector, METHYL 3-AMINO-4-CHLORO-1-BENZOTHIOPHENE-2-CARBOXYLATE is utilized as a building block for the synthesis of agrochemicals. Its incorporation into these products can enhance their effectiveness in agricultural applications, such as pest control and crop protection.
Used in Medicinal Chemistry Research:
METHYL 3-AMINO-4-CHLORO-1-BENZOTHIOPHENE-2-CARBOXYLATE is employed as a key component in medicinal chemistry research. Its versatile structure enables the exploration of new chemical pathways and the development of innovative therapeutic agents.
It is important to handle METHYL 3-AMINO-4-CHLORO-1-BENZOTHIOPHENE-2-CARBOXYLATE with care and adhere to proper safety measures due to its potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 35212-86-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,2,1 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 35212-86:
(7*3)+(6*5)+(5*2)+(4*1)+(3*2)+(2*8)+(1*6)=93
93 % 10 = 3
So 35212-86-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H8ClNO2S/c1-14-10(13)9-8(12)7-5(11)3-2-4-6(7)15-9/h2-4H,12H2,1H3

35212-86-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 3-amino-4-chloro-1-benzothiophene-2-carboxylate

1.2 Other means of identification

Product number -
Other names 3-amino-4-chloro-benzo[b]thiophene-2-carboxylic acid methyl ester

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:35212-86-3 SDS

35212-86-3Relevant academic research and scientific papers

Cu-Catalyzed Denitrogenative Transannulation of 3-Aminoindazoles to Assemble 1-Aminoisoquinolines and 3-Aminobenzothiophenes

Zhou, Yao,Wang, Ya,Lou, Yixian,Song, Qiuling

, p. 8869 - 8873 (2019/09/12)

We disclose a novel Cu-catalyzed denitrogenative transannulation of 3-aminoindazoles to afford diverse functionalized 3-aminobenzothiophenes and 1-aminoisoquinolines, in which denitrogenative transannulation of 3-aminoindazoles is reported for the first t

BENZOFURAN AND BENZOTHIOPHENE DERIVATIVES SUBSTITUTED WITH AMIDE, PROCESS FOR THE PREPARATION THEREOF, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME

-

Page/Page column 23, (2009/05/28)

The present invention relates to a novel benzofuran or benzothiophene derivative substituted with amide. The inventive benzofuran or benzothiophene derivative substituted with amide effectively inhibits ischemic cell death, and thus, can be advantageously

New Synthesis with Elemental Sulfur. - Preparation of 1,2-Benzisothiazoles and Some Secondary Reactions

Markert, Juergen,Hagen, Helmut

, p. 768 - 778 (2007/10/02)

The preparation of new 1,2-benzisothiazoles 2,3,5 and of thienoisothiazole 4 is described.The thioethers 8 have been obtained from 2 and 3 by ring opening with alcoholate and reaction with halomethyl compounds.On cyclisation, the thioethers 8 give the thionaphthenes 11.The ring systems of thionaphthenopyrimidines 10 and 12 have been prepared from 11.

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