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121003-24-5

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121003-24-5 Usage

Chemical structure

Bicyclic heterocyclic compound containing a seven-membered ring with a sulfur atom and a nitrogen atom

Also known as

1-acetylhexahydro-2H-azepine-2-thione

Usage

Building block in organic synthesis, pharmaceutical industry for synthesis of drugs and drug intermediates

Potential applications

Medicinal chemistry, drug development

Check Digit Verification of cas no

The CAS Registry Mumber 121003-24-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,0,0 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 121003-24:
(8*1)+(7*2)+(6*1)+(5*0)+(4*0)+(3*3)+(2*2)+(1*4)=45
45 % 10 = 5
So 121003-24-5 is a valid CAS Registry Number.

121003-24-5SDS

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-(2-Thioxo-azepan-1-yl)-ethanone

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:121003-24-5 SDS

121003-24-5Downstream Products

121003-24-5Relevant articles and documents

A New Synthesis of β-Lactams via Photochemical γ-Hydrogen Abstraction of Monothioimides

Sakamoto, Masami,Watanabe, Shoji,Fujita, Tsutomu,Tohnishi, Masakazu,Aoyama, Hiromu,Omote, Yoshimori

, p. 2203 - 2208 (2007/10/02)

Photochemical reactions of acyclic and semicyclic monothioimides were studied.Photolysis of acyclic monothioimides gave β-lactams (Type II cyclization products) and thioamides (Type II cleavage products). 4-Mercapto-β-lactams were isolated as 4-acylthio-β-lactams by acylation with benzoyl chloride or acetyl chloride in the presence of triethylamine.Irradation of six- or seven- membered semicyclic monothioimides gave bicyclic β-lactams, but five-membered semicyclic monothioimides gave only Type II cleavage products.

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