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Thiazesim is a chemical compound belonging to the class of thiazoles, which are heterocyclic organic molecules containing a sulfur atom and a nitrogen atom in a five-membered ring. These compounds are known for their diverse range of applications, including pharmaceuticals, agrochemicals, and dyes. Thiazesim, in particular, is characterized by its unique structure and properties, which can be further modified through various chemical reactions to create derivatives with specific functionalities. Due to its versatility, Thiazesim and its derivatives have been widely studied for their potential use in the development of new drugs, pesticides, and other industrial applications.

5845-26-1

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5845-26-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5845-26-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,4 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5845-26:
(6*5)+(5*8)+(4*4)+(3*5)+(2*2)+(1*6)=111
111 % 10 = 1
So 5845-26-1 is a valid CAS Registry Number.
InChI:InChI=1/C19H22N2OS/c1-20(2)12-13-21-16-10-6-7-11-17(16)23-18(14-19(21)22)15-8-4-3-5-9-15/h3-11,18H,12-14H2,1-2H3

5845-26-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[2-(dimethylamino)ethyl]-2-phenyl-2,3-dihydro-1,5-benzothiazepin-4-one

1.2 Other means of identification

Product number -
Other names 5-<2-Dimethylamino-aethyl>-4-oxo-2-phenyl-2,3,4,5-tetrahydro-1,5-benzothiazepin

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:5845-26-1 SDS

5845-26-1Downstream Products

5845-26-1Relevant academic research and scientific papers

Asymmetric Hydrogenation of Vinylthioethers: Access to Optically Active 1,5-Benzothiazepine Derivatives

Li, Wei,Schlepphorst, Christoph,Daniliuc, Constantin,Glorius, Frank

, p. 3300 - 3303 (2016/03/22)

A novel asymmetric hydrogenation of vinylthioethers was developed using a ruthenium(II) NHC complex. This method provides an efficient approach to optically active 1,5-benzothiazepines featuring stereocenters with C-S bonds. Excellent enantioselectivities

A 1,5-benzothiazepine synthesis

Phippen, Christopher B.W.,McErlean, Christopher S.P.

supporting information; experimental part, p. 1490 - 1492 (2011/05/16)

The pharmaceutically active compound (±)-thiazesim was synthesized in four steps and 62% overall yield. This new approach to biologically relevant benzothiazepine ring systems features the use of water as a solvent, co-solvent or catalyst in three of the

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