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1-[bis(benzylsulfanyl)methyl]-4-methoxybenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32188-47-9

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32188-47-9 Usage

Type of compound

Benzene derivative

Benzylsulfanyl group

A sulfur-containing group attached to a benzene ring

Methoxy group

An oxygen-containing group attached to a benzene ring

Structure

a. Benzylsulfanyl group attached to a carbon atom
b. Methoxy group attached to another carbon atom

Color

White to light yellow

Physical state

Crystalline powder

Solubility

a. Sparingly soluble in water
b. Soluble in organic solvents

Applications

a. Synthesis of various pharmaceuticals
b. Intermediate in the production of organic compounds

Potential uses

a. Field of medicinal chemistry
b. Organic synthesis

Unique properties

a. Unique chemical structure
b. Reactivity due to the presence of functional groups

Check Digit Verification of cas no

The CAS Registry Mumber 32188-47-9 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 32188-47:
(7*3)+(6*2)+(5*1)+(4*8)+(3*8)+(2*4)+(1*7)=109
109 % 10 = 9
So 32188-47-9 is a valid CAS Registry Number.

32188-47-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[bis(benzylsulfanyl)methyl]-4-methoxybenzene

1.2 Other means of identification

Product number -
Other names Dibenzylthioacetal von p-Methoxybenzaldehyd

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:32188-47-9 SDS

32188-47-9Downstream Products

32188-47-9Relevant academic research and scientific papers

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.

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

TETRACHLOROSILANE CATALYZED DITHIOACETALIZATION

Ku, Bonchul,Oh, Dong Young

, p. 433 - 438 (2007/10/02)

Tetrachlorosilane was found to be a mild as well as selective catalyst for dithioacetalization of the carbonyl compounds.

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