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4431-79-2

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4431-79-2 Usage

Description

([(benzylthio)methyl]thiomethyl)benzene, also known as benzylthiomethylbenzene, is a chemical compound characterized by its molecular formula C15H16S2. It presents as a white crystalline solid with a molecular weight of 260.41 g/mol. This versatile compound is utilized across various industries, particularly in the synthesis of organic compounds and pharmaceuticals, as well as in the production of dyes and perfumes.

Uses

Used in Chemical Industry:
([(benzylthio)methyl]thiomethyl)benzene serves as an intermediate in the synthesis of a variety of organic compounds. Its unique structure allows it to be a key component in creating complex molecules that are used in different chemical processes.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, ([(benzylthio)methyl]thiomethyl)benzene is employed as an intermediate for the development of new drugs. Its properties make it suitable for the synthesis of medicinal compounds that can address various health conditions.
Used in Dye Production:
([(benzylthio)methyl]thiomethyl)benzene is utilized in the production of dyes due to its chemical properties that contribute to the color and stability of the dyes. This makes it a valuable component in the textile and other industries that rely on colorants.
Used in Perfumery:
Its application extends to the creation of perfumes, where ([(benzylthio)methyl]thiomethyl)benzene contributes to the development of unique fragrances. Its role in perfumery is to provide specific scent profiles that can be used in various fragrance formulations.
It is crucial to handle ([(benzylthio)methyl]thiomethyl)benzene with care and adhere to proper safety protocols to ensure the safety of individuals and the environment during its use in these applications.

Check Digit Verification of cas no

The CAS Registry Mumber 4431-79-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,3 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4431-79:
(6*4)+(5*4)+(4*3)+(3*1)+(2*7)+(1*9)=82
82 % 10 = 2
So 4431-79-2 is a valid CAS Registry Number.

4431-79-2SDS

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 benzylsulfanylmethylsulfanylmethylbenzene

1.2 Other means of identification

Product number -
Other names formaldehyde dibenzylthioketal

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:4431-79-2 SDS

4431-79-2Relevant articles and documents

Preparation method of dithioacetal derivative

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Paragraph 0029-0031, (2021/02/10)

The invention discloses a method for preparing a dithioacetal derivative, which specifically comprises the steps of sequentially adding sodium borohydride and thiophenol or mercaptan into a reaction tube filled with a dichloromethane solvent, sealing the

Straightforward chemoselective access to unsymmetrical dithioacetals through a thiosulfonate homologation-nucleophilic substitution sequence

Ielo, Laura,Pillari, Veronica,Gajic, Natalie,Holzer, Wolfgang,Pace, Vittorio

supporting information, p. 12395 - 12398 (2020/10/30)

A sequential C1-homologation-nucleophilic substitution tactic is presented for the preparation of rare unsymmetrical dithioacetals. The judicious selection of thiosulfonates as convenient sulfur electrophilic sources - upon the homologation event conducted on an intermediate a-halothioether - guarantees the release of the non-reactive sulfonate group, thus enabling the subsequent nucleophilic displacement with an external added thiol [(hetero)- aromatic and/or aliphatic]. Uniform high yields and excellent chemocontrol were deduced during the extensive scope study, thus documenting the versatility of the direct technique for the preparation of these unique and manipulable materials.

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