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2,2-dimethyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one is a heterocyclic chemical compound with the molecular formula C12H15NOS. It is a derivative of benzothiazepine, characterized by a benzene ring fused to a thiophene ring. 2,2-dimethyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one is known for its potential pharmaceutical properties and is currently under investigation for its possible applications in treating various medical conditions. Its complex structure and unique characteristics have garnered interest within the scientific community for further research and potential uses in the medical field.

40334-89-2

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40334-89-2 Usage

Uses

Used in Pharmaceutical Industry:
2,2-dimethyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one is used as a pharmaceutical compound for its potential therapeutic effects. 2,2-dimethyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one is being researched for its possible use in the treatment of various medical conditions due to its unique properties and complex structure. Its potential applications in medicine make it a valuable candidate for further study and development.
Used in Research and Development:
2,2-dimethyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one is used as a subject of scientific research for its potential applications in medicine. 2,2-dimethyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one's unique properties and complex structure make it an interesting area of study for researchers seeking to understand its potential benefits and develop new treatments based on its characteristics.

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 academic research and scientific papers

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

Oxazepines and thiazepines, XXV: Chemical transformations of 2,3-dihydro-1,5-benzothiazepin-4(5H)-ones

Levai

, p. 721 - 726 (2007/10/02)

2,3-Dihydro-1,5-benzothiazepine-4(5H)-thiones 13-22 were prepared by the reaction of the appropriate 2,3-dihydro-1,5-benzothiazepin-4(5H)-ones with Lawesson's reagent. N-Acyl (23-25) and N-alkyl (26-28) derivatives have also been synthesized. Oxidation wi

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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