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4H-1-Benzothiopyran, 5,6,7,8-tetrahydro-2,4-diphenyl- is a chemical compound belonging to the benzothiopyran family, characterized by a benzene ring fused with a thiopyran ring. This specific compound features a tetrahydro structure, meaning it has four hydrogen atoms attached to the carbon atoms in the ring, and two phenyl groups (C6H5) attached to the 2nd and 4th positions of the benzothiopyran core. The compound is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the production of other organic compounds. Its chemical formula is C20H18S, and it is often represented by the CAS number 23978-65-4.

7584-37-4

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7584-37-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7584-37-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,8 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7584-37:
(6*7)+(5*5)+(4*8)+(3*4)+(2*3)+(1*7)=124
124 % 10 = 4
So 7584-37-4 is a valid CAS Registry Number.

7584-37-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-diphenyl-5,6,7,8-tetrahydro-4H-thiochromene

1.2 Other means of identification

Product number -
Other names 2,4-Diphenyl-5,6-tetramethylene-4H-thiopyran

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:7584-37-4 SDS

7584-37-4Relevant academic research and scientific papers

REDOX PROPERTIES OF 2,4-DIARYL-SUBSTITUTED CYCLOHEXATHIOPYRYLIUM SALTS

Ivanova, N. N.,Berberova, N. T.,Archegova, A. S.,Klivov, E. S.,Shpakov, A. V.,et al.

, p. 292 - 296 (2007/10/02)

A scheme for formation of 6,6',7'7'-tetrahydro-2,2',4,4'-tetraaryl-8,8'-bis(5H-1-benzothiopyranyls) through intermediate radicals and cation radicals was substantiated as a result of a study of the electrochemical behavior of 2,4-diarylcyclohexathiopyr

CATALYTIC REDUCTION OF THIOPYRYLIUM SALTS AND THEIR CONDENSED ANALOGS

Kharchenko, V. G.,Bozhenova, O. A.,Shebaldova, A. D.

, p. 2158 - 2162 (2007/10/02)

A method was developed for the synthesis of substituted thiacyclohexanes, thiadecalins, and perhydrothioxanthenes by reduction of thiopyrylium salts and their condensed analogs under the conditions of catalytic hydrogenation in the presence of catalysts b

INTERCONVERSIONS, REACTIVITIES, AND STRUCTURES OF ISOMERIC HYDROTHIOCHROMENES

Stolbova, T. V.,Klimenko, S. K.,Shcherbakov, A. A.,Andrianov, V. G.,Struchkov, Yu. T.,et al.

, p. 1002 - 1006 (2007/10/02)

2,4-Diphenyl-5,6,7,9-tetrahydrothiochromene was isomerized to 2,4-diphenyl-5,6-tetramethylene-4H-thiopyran in the presence of HCl and DCl.The relative thermodynamic stabilities of 2,4-diphenyl-5,6-tetramethylene-6H-thiopyran and the compound thus obtaione

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