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17402-82-3

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17402-82-3 Usage

General Description

Benzo[b]thiophen-3-ylamine, also known as 3-Aminobenzothiophene, is a chemical compound that belongs to the class of thiophene derivatives. It consists of a benzene ring fused to a thiophene ring with an amino group attached at the third position of the thiophene ring. Benzo[b]thiophen-3-ylamine is used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is also used in research and development as a starting material for the preparation of biologically active molecules. Benzo[b]thiophen-3-ylamine has potential applications in the field of medicinal chemistry and drug discovery due to its pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 17402-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,0 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17402-82:
(7*1)+(6*7)+(5*4)+(4*0)+(3*2)+(2*8)+(1*2)=93
93 % 10 = 3
So 17402-82-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H7NS/c9-7-5-10-8-4-2-1-3-6(7)8/h1-5H,9H2

17402-82-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzothiophen-3-amine

1.2 Other means of identification

Product number -
Other names 3-Aminobenzothiophene

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:17402-82-3 SDS

17402-82-3Relevant articles and documents

Functionalization of C-H bonds in acetophenone oximes with arylacetic acids and elemental sulfur

Nguyen, Khang X.,Nguyen, Tung T.,Pham, Hoai T. B.,Pham, Phuc H.,Phan, Nam T. S.,Tran, Thien T.

, p. 11024 - 11032 (2020/04/03)

Fused thieno[3,2-d]thiazoles were synthesized via a coupling of acetophenone ketoximes, arylacetic acids, and elemental sulfur in the presence of Li2CO3 base. Functionalities including chloro, bromo, fluoro, trifluoromethyl, and pyridyl groups were compatible with reaction conditions. High yields and excellent regioselectivities were obtained even if meta-substituted ketoxime acetates were used. Ethyl esters of heteroarylacetic acids were competent substrates, which is very rare in the literature. Our method would offer a convenient protocol to afford polyheterocyclic structures from simple substrates.

Homo- A nd Heteroannulation of sp3 C-H Bonds in Acetophenones for Divergent Synthesis of Thienothiazoles

Pham, Phuc H.,Nguyen, Khang X.,Pham, Hoai T. B.,Nguyen, Tung T.,Phan, Nam T. S.

supporting information, p. 8795 - 8799 (2019/11/11)

A synthesis of fused thieno[3,2-d]thiazoles via direct functionalization of C(sp3)-H bonds in acetophenones was reported. The transformation is divergent to afford either 2-phenylbenzo[4,5]thieno[3,2-d]thiazoles or benzo[4,5]thieno[3,2-d]thiazo

Synthesis and properties of symmetric and unsymmetric dibenzothienopyrroles

Balaji, Ganapathy,Valiyaveettil, Suresh

supporting information; experimental part, p. 3358 - 3361 (2009/12/03)

Symmetrical and unsymmetrical heteroacenes containing thiophene and pyrrole rings were synthesized. The unsymmetrical heteroacene was synthesized in two steps involving an unexpected palladium catalyzed amination of alkyl or aryl amines with benzo[b]thiop

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