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92814-42-1

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92814-42-1 Usage

General Description

(R)-6-amino-1,4-thiazepan-5-one is a chemical compound with the molecular formula C5H10N2OS. It is a heterocyclic organic compound that contains a thiazepane ring with an amino group at the 6th carbon and a carbonyl group at the 5th carbon. (R)-6-amino-1,4-thiazepan-5-one has potential pharmaceutical applications, particularly in the development of novel drugs for neurological and psychiatric disorders. It is also being researched for its potential use in treating mood disorders and anxiety. Additionally, (R)-6-amino-1,4-thiazepan-5-one has been investigated for its anti-inflammatory and immunomodulatory properties, making it a potentially important compound for the development of new therapies for various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 92814-42-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,8,1 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 92814-42:
(7*9)+(6*2)+(5*8)+(4*1)+(3*4)+(2*4)+(1*2)=141
141 % 10 = 1
So 92814-42-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H10N2OS/c6-4-3-9-2-1-7-5(4)8/h4H,1-3,6H2,(H,7,8)

92814-42-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (6R)-6-amino-1,4-thiazepan-5-one

1.2 Other means of identification

Product number -
Other names (6R)-6-aminotetrahydro-1,4-thioazepin-5(2H)-one

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:92814-42-1 SDS

92814-42-1Relevant articles and documents

Synthesis and evaluation of thiazepines as interleukin-1β converting enzyme (ICE) inhibitors

Ellis, Christopher D.,Oppong, Kofi A.,Laufersweiler, Michael C.,O'Neil, Steven V.,Soper, David L.,Wang, Yili,Wos, John A.,Fancher, Amy N.,Lu, Wei,Suchanek, Maureen K.,Wang, Richard L.,De, Biswanath,Demuth Jr., Thomas P.

, p. 4728 - 4732 (2007/10/03)

A series of monocyclic thiazepine inhibitors of interleukin-1β converting enzyme (ICE) were synthesized in eight steps from commercially available intermediates. In vitro biological evaluation showed the thiazepines to be moderately potent ICE inhibitors,

DERIVATIVES OF AZEPINE AND THIAZERAN AS INTERLEUKIN CONVERTING ENZYME INHIBITORS

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Page 87, (2010/02/04)

The present invention relates to interleukin - Iβ converting enzyme inhibitors of formula I: wherein each X is independently selected from: i) -C(W)2-; ii) -C(O)-; iii) -NR2-; iv) -S-; v) -S(O)-; vi) -S(O)2-; vii) two units, one from each adjacent X unit,

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