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10486-58-5

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10486-58-5 Usage

General Description

2-Mercaptobenzselenazole is a chemical compound with the molecular formula C7H5NSeS. It is a selenazole derivative that contains a benzene ring and a selenium atom attached to a thiol group. 2-MERCAPTOBENZSELENAZOLE has been studied for its potential pharmaceutical and industrial applications, including its use as an antioxidant and as a pharmaceutical agent in the treatment of various diseases. 2-Mercaptobenzselenazole has also been researched for its antimicrobial and antiparasitic properties, as well as its potential use in the development of new materials and chemical processes. Its unique structure and properties make it a versatile and important compound in the field of chemistry and medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 10486-58-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,8 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10486-58:
(7*1)+(6*0)+(5*4)+(4*8)+(3*6)+(2*5)+(1*8)=95
95 % 10 = 5
So 10486-58-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H5NSSe/c9-7-8-5-3-1-2-4-6(5)10-7/h1-4H,(H,8,9)

10486-58-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3H-1,3-benzoselenazole-2-thione

1.2 Other means of identification

Product number -
Other names 3H-Benzoselenazol-2-thion

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:10486-58-5 SDS

10486-58-5Relevant articles and documents

Synthesis of diselenadiazafulvalenes and influence of steric strain on their anodic behavior

Casar, Zdenko,Leban, Ivan,Marechal, Alenka Majcen-Le,Lorcy, Dominique

, p. 1568 - 1573 (2002)

A novel family of π-donor molecules, the diselenadiazafulvalenes (DSeDAFs), is presented. The synthetic approach to these donors, from o-nitroaniline, allows the formation of N,N′-dimethyldibenzo DSeDAF and N,N′-ethylenedibenzo DSeDAF. Comparative electrochemical study of these π-donor molecules demonstrates their excellent donor ability and the stabilizing effect of the ethylene bridge on the cation radical species.

The Importance of 1,5-Oxygen???Chalcogen Interactions in Enantioselective Isochalcogenourea Catalysis

Cockroft, Scott L.,Elmi, Alex,Frost, Aileen B.,Ling, Kenneth B.,McLaughlin, Calum,Morris, Rylie K.,Pascoe, Dominic J.,Slawin, Alexandra M. Z.,Smith, Andrew D.,Smith, Terry K.,Willoughby, Patrick H.,Woods, Andrew M.,Young, Claire M.,de la Houpliere, Alix

supporting information, p. 3705 - 3710 (2020/02/11)

The importance of 1,5-O???chalcogen (Ch) interactions in isochalcogenourea catalysis (Ch=O, S, Se) is investigated. Conformational analyses of N-acyl isochalcogenouronium species and comparison with kinetic data demonstrate the significance of 1,5-O???Ch interactions in enantioselective catalysis. Importantly, the selenium analogue demonstrates enhanced rate and selectivity profiles across a range of reaction processes including nitronate conjugate addition and formal [4+2] cycloadditions. A gram-scale synthesis of the most active selenium analogue was developed using a previously unreported seleno-Hugerschoff reaction, allowing the challenging kinetic resolutions of tertiary alcohols to be performed at 500 ppm catalyst loading. Density functional theory (DFT) and natural bond orbital (NBO) calculations support the role of orbital delocalization (occurring by intramolecular chalcogen bonding) in determining the conformation, equilibrium population, and reactivity of N-acylated intermediates.

Meso-ionic se- and s-containing tetrazoles

-

, (2008/06/13)

This invention relates to meso-ionic tetrazole compounds of the formula: STR1 wherein X- is -S- or -Se- which are useful as photographic additives and to an intermediate useful in the preparation thereof having the formula: STR2

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