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Dimethallyl sulphide, with the chemical formula CH2=CHCH2SCH2CH=CH2, is a highly reactive oily liquid characterized by a pungent garlic-like odor. It is a naturally occurring compound found in garlic and other Allium family members, contributing to their distinctive smell. Studies have explored its potential health benefits, such as anti-inflammatory and anti-cancer properties, while also noting its potential toxicity and irritancy at high concentrations.

52444-06-1

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52444-06-1 Usage

Uses

Used in Flavoring Industry:
Dimethallyl sulphide is utilized as a flavoring agent in food products, capitalizing on its characteristic garlic-like aroma to enhance the taste and appeal of various culinary creations.
Used in Traditional Medicine:
In traditional medicine, dimethallyl sulphide is considered a potential therapeutic compound, harnessing its anti-inflammatory and anti-cancer properties for the treatment and management of specific health conditions. However, its use is carefully regulated due to the associated risks of toxicity and irritation at high concentrations.

Check Digit Verification of cas no

The CAS Registry Mumber 52444-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,4 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 52444-06:
(7*5)+(6*2)+(5*4)+(4*4)+(3*4)+(2*0)+(1*6)=101
101 % 10 = 1
So 52444-06-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H14S/c1-7(2)5-9-6-8(3)4/h1,3,5-6H2,2,4H3

52444-06-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-4-amino-N-[(1R,2S,3S,4R,5S)-5-amino-4-[(2R,3R,6S)-3-amino-6-(aminomethyl)oxan-2-yl]oxy-2-[(2S,3R,4S,5S,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-hydroxycyclohexyl]-2-hydroxybutanamide

1.2 Other means of identification

Product number -
Other names Arbekacina

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:52444-06-1 SDS

52444-06-1Downstream Products

52444-06-1Relevant academic research and scientific papers

Selectivity between deprotonation and attack on tellurium in the reaction of 1,4-thiatellurins with strongly basic reagents

Schoufs, H.J.M.,Maercker, A.,Brandsma, L.

, p. 1 - 6 (1992)

Reaction of 1,4-thiatellurin and some of its alkyl derivatives with n-butyllithium in tetrahydrofuran gives Z,Z-2,2'-dilithiodivinyl sulfide or alkyl derivatives and dibutyl telluride.With lithium diisopropylamide in tetrahydrofuran, in the case of 3,5'-dialkyl-1,4-thiatellurins, deprotonation with concomitant ring opening is the main reaction.

α,α'-DIIDOSULFIDES A USEFUL PREPARATION OF DIVINYLIC SULFIDES

Aida, T.,Chan, T. H.,Harpp, David N.

, p. 1089 - 1092 (2007/10/02)

Symmetric and unsymmetric divinylic sulfides can be prepared almost quantitatively by the elimination of HI by base from the corresponding α,α'-diidosulfide.These molecules are quantitatively formed in situ from α,α'-bistrimethylsiloxysulfides and iodotri

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