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1,3-Dithiolane, 2,2-diphenyl-, 1-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92548-83-9

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92548-83-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92548-83-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,5,4 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 92548-83:
(7*9)+(6*2)+(5*5)+(4*4)+(3*8)+(2*8)+(1*3)=159
159 % 10 = 9
So 92548-83-9 is a valid CAS Registry Number.

92548-83-9SDS

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 2,2-diphenyl-1,3-dithiolane S-oxide

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:92548-83-9 SDS

92548-83-9Relevant academic research and scientific papers

ENANTIOSELECTIVE OXIDATION OF CYCLIC DITHIOACETALS AND DITHIOKETALS

Furia, Fulvio Di,Licini, Giulia,Modena, Giorgio

, p. 165 - 170 (2007/10/02)

The asymmetric oxidation of a series of dithio acetals and dithio ketals to their corresponding monosulphoxides by the procedure developed in our laboratory has been carried out.Simple 1,3-dithiolanes pr

PHOTOSENSITIZED ELECTRON TRANSFER OXIDATION OF 2-SUBSTITUTED 1,3-DITHIOLANE TO 1,3-DITHIOLANE-1-OXIDE

Pandey, Bipin,Bal, Smita Y.,Khire, Uday R.

, p. 4007 - 4008 (2007/10/02)

Irradation of a solution of 1,3-dithiolane, 1-cyanonaphthalene in O2-saturated CH3CN:H2O (3:1) at 350 nm furnishes good yields of 1,3-dithiolane-1-oxide.

Thioketones and Enethiolates by 1,3-Anionic Cycloreversion of Dithiolane Derivatives

Schaumann, Ernst,Ruehter, Gerd

, p. 1159 - 1164 (2007/10/02)

The reactive (ar)aliphatic thioketones 3a-c are generated by cycloreversion of the anions 2 of 1,3-dithiolane-4,5-dicarboxylates 1 and are trapped by mesitonitrile oxide (5) in a 1,3-dipolar cycloaddition to give 7.From the fragmentation of anions 12 of 1,3-dithiolane 1,1-dioxides 11, thiobenzophenone (3d) and thiocamphor (3e) are isolated, wheras thioketones 3a,c with α-hydrogen are deprotonated in situ to provide enethiolates 13.Anions 13 add nitrile oxide 5 to yield thiohydroximates 8.

The Lithium Diisopropylamide-Induced Fragmentation of 2,2-Diphenyl-1,3-dithiolane S-Oxide and Several 2,2-Diaryl-1,3-dithiolane S,S'-Dioxides

Inoue, Yoshihiko,Tanimoto, Shigeo,Oida, Tatsuo

, p. 3897 - 3900 (2007/10/02)

The reaction of 2,2-diphenyl-1,3-dithiolane S-oxide with lithium diisopropylamide results in fragmentation to thiobenzophenone followed by further conversion leading to alkyl diphenylmethyl sulfide on trapping with alkyl halide.The reaction of 2,2-diaryl-

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