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2-(1,3-dioxo-1,3-diphenyl-propan-2-yl)disulfanyl-1,3-diphenyl-propane-1,3-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72087-95-7

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72087-95-7 Usage

Molecular structure

Contains two disulfanyl groups and multiple phenyl groups, making it a highly conjugated molecule.

Functional groups

Di酮 (1,3-dione) and disulfanyl groups are present in the compound.

Potential applications

May have applications in organic synthesis and as a reagent in chemical reactions.

Laboratory handling

Due to its complex structure and potential reactivity, it must be handled and used with caution in a laboratory setting.

Further study

Exact properties and potential uses would likely need to be determined through additional research and experimentation.

Check Digit Verification of cas no

The CAS Registry Mumber 72087-95-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,0,8 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 72087-95:
(7*7)+(6*2)+(5*0)+(4*8)+(3*7)+(2*9)+(1*5)=137
137 % 10 = 7
So 72087-95-7 is a valid CAS Registry Number.

72087-95-7SDS

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-[(1,3-dioxo-1,3-diphenylpropan-2-yl)disulfanyl]-1,3-diphenylpropane-1,3-dione

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

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:72087-95-7 SDS

72087-95-7Upstream product

72087-95-7Relevant academic research and scientific papers

Selenosilane-Promoted Selective Mild Transformation of N -Thiophthalimides into Symmetric Disulfides

Viglianisi, Caterina,Bonardi, Chiara,Ermini, Elena,Capperucci, Antonella,Menichetti, Stefano,Tanini, Damiano

, p. 1819 - 1824 (2019/04/05)

The reactivity of N -thiophthalimides with silyl chalcogenides is described. Treatment of N -thiophthalimides with bis(trimethylsilyl) sulfide [(Me 3 Si) 2 S] leads to the formation of a mixture of the corresponding disulfides and tr

APPROACHES TO THE LIBERATION OF THIOSULFINES

Franek, Walter

, p. 381 - 382 (2007/10/02)

In 1979 A.Senning found a series of reactions that involve probably thiosulfines of thiocarbonyl S-sulfides.Now, disulfide 5a was chosen for a re-examination, as no rearrangements seem to be involved.F, Cl, Br, CH3, and CH3O are used to change the electro

SCHWEFELHALTIGE DERIVATIVE DES DIBENZOYLMETHANS.

Senning, Alexander

, p. 323 - 326 (2007/10/02)

A number of sulfur-containing derivatives of dibenzoylmethane were obtained by conversions involving the active methylene group.

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