57500-00-2 Usage
Description
Methyl furfuryl disulfide is an organic compound with a distinct berry, fruity, and vegetable odor and flavor. It is commonly found in various food items such as wheat bread, pork, liver, coffee, and malt.
Uses
Used in Flavor Industry:
Methyl furfuryl disulfide is used as a flavoring agent for its characteristic berry, fruity, and vegetable flavor. It adds a unique taste to the products, enhancing their overall flavor profile.
Used in Fragrance Industry:
Methyl furfuryl disulfide is used as a component in the creation of various fragrances due to its pleasant and distinctive odor. It contributes to the development of scents that are reminiscent of berries, fruits, and vegetables, making it a valuable addition to the fragrance industry.
Used in Food Industry:
Methyl furfuryl disulfide is used as an additive in the food industry to impart a specific flavor to various products. Its natural occurrence in certain food items makes it a suitable choice for enhancing the taste and aroma of different dishes and food products.
Used in Cosmetic Industry:
Methyl furfuryl disulfide can be used in the cosmetic industry for its pleasant odor, potentially being incorporated into products like perfumes, body lotions, and other personal care items to provide a fresh and appealing scent.
Check Digit Verification of cas no
The CAS Registry Mumber 57500-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,5,0 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 57500-00:
(7*5)+(6*7)+(5*5)+(4*0)+(3*0)+(2*0)+(1*0)=102
102 % 10 = 2
So 57500-00-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H8OS2/c1-8-9-5-6-3-2-4-7-6/h2-4H,5H2,1H3
57500-00-2Relevant articles and documents
NFSI-catalyzed S[sbnd]S bond exchange reaction for the synthesis of unsymmetrical disulfides
Hu, Qingyue,Li, Zheng-Yi,Song, Mengjie,Sun, Xiaoqiang,Yang, Ke
supporting information, (2022/01/26)
The metal-free S[sbnd]S bond exchange reaction of symmetrical disulfides catalyzed by NFSI is described. This novel protocol provides a facile and efficient approach to accessing important unsymmetrical disulfides. Furthermore, this strategy could also be utilized in the late-stage functionalization of amino acids, drugs, and natural products. The broad substrate scope, good functional group tolerance and easy accessibility of catalyst indicate that this strategy affords a green and practical complementary method to various unsymmetrical disulfides.
Potassium fluoride on alumina: A convenient synthesis of O-alkyl methyldithiocarbonates. Pyrolysis of O-benzyl-S-methyldithiocarbonates
Villemin, Didier,Hachemi, Messaoud
, p. 2449 - 2459 (2007/10/03)
Xanthates were easily prepared by adsorption of alcohol on KF-Al2O3 followed by treatment of carbon disulfide and iodomethane at room temperature. Pyrolysis of benzyl xanthate affords to a complex mixture of products. A radical process was proposed to explain the nature of products obtained.
The Reaction of Ph3P+SR with Thiols: A Simple, Efficient Synthesis of Unsymmetrical Disulphides
Masui, Masaichiro,Mizuki, Yasuyuki,Sakai, Kiyoshi,Ueda, Chihiro,Ohmori, Hidenobu
, p. 843 - 844 (2007/10/02)
Reaction of Ph3P+SRClO4-, prepared electrochemically from RSSR and Ph3P, with thiols in n-hexane at room temperature gave unsymmetrical disulphides in excellent yields with recovery of Ph3P.
