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Benzene, 1-[bis[(phenylmethyl)thio]methyl]-4-bromo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32188-44-6

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32188-44-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32188-44-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,1,8 and 8 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 32188-44:
(7*3)+(6*2)+(5*1)+(4*8)+(3*8)+(2*4)+(1*4)=106
106 % 10 = 6
So 32188-44-6 is a valid CAS Registry Number.

32188-44-6Downstream Products

32188-44-6Relevant academic research and scientific papers

A mild and chemoselective dithioacetalization of aldehydes in the presence of anhydrous copper (II) sulfate

Moghaddam, Firouz Matloubi,Bardajee, Ghasem Rezanejade,Oskui, Afsane Arefi

, p. 1445 - 1450 (2006)

Various aldehydes have been protected with different thiols as dithioacetals with excellent yields using anhydrous copper sulfate as a mild and chemoselective catalyst. The reaction is carried out in a solvent and/or under solvent-free conditions. The transthioacetalization of oxyacetals into dithioacetals was also achieved in an excellent yield. Copyright Taylor & Francis Group, LLC.

Direct Synthesis of Unsymmetrical Dithioacetals

Bognar, Sabine,van Gemmeren, Manuel

supporting information, p. 4859 - 4863 (2021/02/03)

Dithioacetals are a frequently used motif in synthetic organic chemistry and have recently seen increasing attention as structural motif in promising antiviral agents against plant pathogens. Most existing reports, however, only discuss symmetrical dithioacetals. Examples of mixed dithioacetals are scarce and no general method for the selective synthesis of these compounds exists. Herein, a synthetically simple general one-step protocol was developed for the synthesis of a broad range of unsymmetrical dithioacetals consisting of one aromatic and one aliphatic thiol moiety from the corresponding aldehyde/thiol mixture. The mixed S,S-acetals were obtained in high yields, and a great variety of functional groups was tolerated. Kinetic control enabled an excellent selectivity in regard to the unsymmetrical dithioacetal.

λ3-Iodanes as Visible Light Photocatalyst in Thioacetalization of Aldehydes

Choudhuri, Khokan,Pramanik, Milan,Mal, Prasenjit

supporting information, p. 4822 - 4826 (2019/07/31)

Introduction of an iodine(III) reagent as visible-light photocatalyst for chemoselective dithioacetalization has been the limelight of the current methodology. The mechanistic investigations reveal that the reactions proceeded via radical pathway upon lig

Silica-supported phosphorus pentoxide: A reusable catalyst for S,S-acetalization of carbonyl groups under ambient conditions

Shaterian, Hamid Reza,Azizi, Kobra,Fahimi, Nafiseh

experimental part, p. 85 - 91 (2012/01/06)

Phosphorus pentoxide supported on silica gel (P2O 5/SiO2) efficiently acts as a highly active and reusable catalyst for cyclic and non-cyclic S,S-acetalization of a variety of carbonyl compounds under mild, solvent-free an

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