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5-(4-methoxyphenyl)-1,3-thiaselenole-2-thione is an organic compound with the molecular formula C9H7OSeS. It is a derivative of 1,3-thiaselenole, which is a heterocyclic compound containing selenium and sulfur atoms. The compound features a 4-methoxyphenyl group attached to the 5-position of the thiaselenole ring, providing it with unique chemical and physical properties. This molecule is of interest in the field of organic chemistry, particularly in the synthesis of various selenium-containing compounds and their potential applications in materials science, pharmaceuticals, and agrochemicals. Its structure and reactivity make it a valuable building block for the development of new molecules with specific properties and functions.

65456-33-9

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65456-33-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65456-33-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,5 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 65456-33:
(7*6)+(6*5)+(5*4)+(4*5)+(3*6)+(2*3)+(1*3)=139
139 % 10 = 9
So 65456-33-9 is a valid CAS Registry Number.

65456-33-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-methoxyphenyl)-1,3-thiaselenole-2-thione

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

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More Details:65456-33-9 SDS

65456-33-9Relevant academic research and scientific papers

UNSATURATED THIOLATES AND THEIR ANALOGS IN CYCLOADDITION REACTIONS. XIII. REACTIONS OF POTASSIUM 2-ARYL- AND 2-ALKYLETHYNESELENOLATES WITH HETEROCUMULENES

Laishev, V. Z.,Petrov, M. L.,Petrov, A. A.

, p. 450 - 454 (2007/10/02)

Potassium 2-aryl- and 2-alkylethyneselenolates, obtained by the decomposition of 4-substituted 1,2,3-selenadiazoles, enter into a cyclization reaction with phenyl isothiocyanate to form isomeric N-(5-R-1,3-thiaselenol-2-ylidene)phenylamines.Measurement of the relative rate constants for cyclization of 2-(p-R-aryl)ethyneselenolates at the thione bond shows that the reaction is accelerated by donating substituents and retarded by withdrawing substituents.

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