54644-28-9 Usage
Description
1,2,4-Trithiolane, 3,5-diethylis an organic compound with a characteristic sulfur odor. It is reportedly present in garlic (Allium sativum L.) and exists in two isomers, (+/-)-cis and trans, with distinct aroma threshold values in water.
Uses
Used in Flavor Industry:
1,2,4-Trithiolane, 3,5-diethylis used as a flavoring agent for its distinct sulfur odor. 1,2,4-Trithiolane, 3,5-diethyl-'s aroma threshold values in water for the cis isomer (0.000032 ppm) and the trans isomer (0.000015 ppm) make it suitable for enhancing the flavor of various food products.
Used in Aroma Industry:
1,2,4-Trithiolane, 3,5-diethylis used as an aroma additive in the perfumery and fragrance industry. The unique sulfur odor of this compound can contribute to the creation of various scent profiles, adding depth and complexity to perfumes and other fragrance products.
Used in Chemical Research:
1,2,4-Trithiolane, 3,5-diethylcan be utilized in chemical research and development, particularly in the study of sulfur-containing compounds and their applications in various fields, such as pharmaceuticals, materials science, and environmental science.
Preparation
Reportedly produced in a patented process from filamentous fungi by heating them in water at a temperature sufficient to
reduce their nucleic acid content. The resulting aqueous solution is concentrated to separate the solids
Check Digit Verification of cas no
The CAS Registry Mumber 54644-28-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,4 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 54644-28:
(7*5)+(6*4)+(5*6)+(4*4)+(3*4)+(2*2)+(1*8)=129
129 % 10 = 9
So 54644-28-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H12S3/c1-3-5-7-6(4-2)9-8-5/h5-6H,3-4H2,1-2H3
54644-28-9Relevant articles and documents
1,3,5-Trithianes and sulfur monochloride/sodium sulfide: an alternative route to 3,5-disubstituted 1,2,4-trithiolanes
Tanini, Damiano,Trapani, Francesca,Capperucci, Antonella
, p. 635 - 644 (2020/09/01)
Treatment of substituted 1,3,5-trithianes with S2Cl2 and Na2S under mild conditions provides 3,5-disubstituted 1,2,4-trithiolanes, as mixture of diastereoisomers.
DIMERES ET OLIGOMERES DES DITHIOACIDES ALIPHATIQUES OBTENUS PAR ACTION DE PEROXYDES OU DU RAYONNEMENT U. V.
Bonnans-Plaisance, Chantal,Mahjoub, Ahmed,Levesque, Guy
, p. 1941 - 1942 (2007/10/02)
Carbodithioic acids when heated with peroxydes lead to linear oligomers whose thermolysis gives rise to trithiolannes and tetrathiannes; U V irradiation leads to tetrathianne and cyclic oligomers.
