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2-[(4-bromophenyl)sulfanyl]ethanamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79270-75-0

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79270-75-0 Usage

Physical state

Colorless to light yellow liquid

Odor

Slightly unpleasant

Usage

Building block for various drugs and pharmaceuticals, key intermediate in the synthesis of pharmacologically active molecules, reagent in the preparation of other chemical compounds

Potential applications

Medicinal chemistry, drug development

Safety

Handle with caution, follow proper safety protocols

Check Digit Verification of cas no

The CAS Registry Mumber 79270-75-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,7 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79270-75:
(7*7)+(6*9)+(5*2)+(4*7)+(3*0)+(2*7)+(1*5)=160
160 % 10 = 0
So 79270-75-0 is a valid CAS Registry Number.

79270-75-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-bromophenyl)sulfanylethanamine,hydrochloride

1.2 Other means of identification

Product number -
Other names -

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:79270-75-0 SDS

79270-75-0Relevant academic research and scientific papers

Synthesis of 2,3,4,5-Tetrahydrobenzo[1,4]thiazepines via N-Acyliminium Cyclization

Deng, Shixian,Cheng, Zhenzhuang,Ingalls, Charles,Kontes, Ferenc,Yan, Jiaming,Belvedere, Sandro

, p. 1801 - 1805 (2017/11/24)

We report an efficient and scalable synthesis of 7-methoxy-2,3,4,5-tetrahydrobenzo[1,4]thiazepine, the core structure of biologically active molecules like JTV-519 and S107. This synthetic route, starting with 4-methoxythiophenol and proceeding via acyliminum cyclization, gives the target product in four steps and 68% overall yield and is a substantial improvement over previously published processes. Nine additional examples of tetrahydrobenzo[1,4]thiazepine synthesis via acyliminium ring closure are also presented.

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