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40334-89-2

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40334-89-2 Usage

General Description

2,2-dimethyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one is a chemical compound with the molecular formula C12H15NOS. It is a derivative of benzothiazepine, a heterocyclic compound with a benzene ring fused to a thiophene ring. 2,2-dimethyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one has potential pharmaceutical properties and is being researched for its potential use in the treatment of various medical conditions. Due to its complex structure and unique properties, 2,2-dimethyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one is of interest to the scientific community for further study and potential applications in medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 40334-89-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,3 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 40334-89:
(7*4)+(6*0)+(5*3)+(4*3)+(3*4)+(2*8)+(1*9)=92
92 % 10 = 2
So 40334-89-2 is a valid CAS Registry Number.

40334-89-2SDS

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 2,3-dihydro-2,2-dimethyl-1,5-benzothiazepin-4(5H)-one

1.2 Other means of identification

Product number -
Other names 2,2-dimethyl-2,3-dihydro-5H-benzo[b][1,4]thiazepin-4-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:40334-89-2 SDS

40334-89-2Relevant articles and documents

N-Heteroaryl glycinamides and glycinamines as potent NPY5 antagonists

Wu, Lingyun,Lu, Kai,Desai, Mahesh,Packiarajan, Mathivanan,Joshi, Amita,Marzabadi, Mohammad R.,Jubian, Vrej,Andersen, Kim,Chandrasena, Gamini,Boyle, Noel J.,Walker, Mary W.

scheme or table, p. 5573 - 5576 (2011/10/09)

Subtype specific ligands are needed to evaluate the therapeutic potential of modulating the brain's neuropeptide Y system. The benzothiazepine glycinamide 1a was identified as an NPY5 antagonist lead. While having acceptable solubility, the compound was f

REACTIONS OF o-AMINOTHIOPHENOL WITH α,β-UNSATURATED DICARBONYL SYSTEMS. FACILE SYNTHESIS OF BENZOTHIAZINES AND BENZOTHIAZEPINES

Balasubramaniyan, V.,Balasubramaniyan, P.,Shaikh, A. S.

, p. 2731 - 2738 (2007/10/02)

When treated with maleanilic/fumaranilic acids or esters or the corresponding imides or isoimides, o-aminothiophenol furnishes benzothiazines, whereas treatment of o-aminothiophenol with acrylic acids/esters furnishes benzothiazepines.The orientational pr

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