52444-06-1 Usage
General Description
Dimethallyl sulphide is a chemical compound with the formula CH2=CHCH2SCH2CH=CH2. It is a highly reactive oily liquid with a pungent garlic-like odor. Dimethallyl sulphide is found in garlic and other members of the Allium family, and it is responsible for the characteristic smell associated with these plants. DIMETHALLYL SULPHIDE has been studied for its potential health benefits, including its anti-inflammatory and anti-cancer properties. However, it can also be toxic in high concentrations and may cause irritation to the eyes, skin, and respiratory tract. Dimethallyl sulphide is used as a flavoring agent in food products and as a potential therapeutic compound in traditional medicine.
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
52444-06-1Relevant articles and documents
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
