22946-45-8 Usage
Uses
Used in Fragrance Industry:
(TRIS-METHYLSULFANYL-VINYL)-BENZENE is used as a fragrance ingredient for its distinctive scent, contributing to the creation of perfumes and personal care products. Its strong odor makes it a valuable addition to the fragrance industry.
Used in Organic Synthesis:
In the field of organic chemistry, (TRIS-METHYLSULFANYL-VINYL)-BENZENE serves as a key component in the synthesis of various organic compounds. Its unique structure allows for the development of a wide range of chemical products.
Used in Food Industry:
(TRIS-METHYLSULFANYL-VINYL)-BENZENE is also utilized as a flavoring agent in the food industry, where its strong scent can enhance the taste and aroma of different products.
Used in Antioxidant and Antimicrobial Applications:
Research has explored the potential antioxidant and antimicrobial properties of (TRIS-METHYLSULFANYL-VINYL)-BENZENE, which could lead to its use in various applications where these properties are beneficial.
Safety Precautions:
It is crucial to handle (TRIS-METHYLSULFANYL-VINYL)-BENZENE with care, as it may cause irritation to the skin, eyes, and respiratory system. Proper safety measures should be taken to minimize any adverse effects during its use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 22946-45-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,4 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22946-45:
(7*2)+(6*2)+(5*9)+(4*4)+(3*6)+(2*4)+(1*5)=118
118 % 10 = 8
So 22946-45-8 is a valid CAS Registry Number.
22946-45-8Relevant academic research and scientific papers
Highly stereoselective one-pot procedure to prepare bis- and tris-chalcogenide alkenes via addition of disulfides and diselenides to terminal alkynes
Moro, Angelica Venturini,Nogueira, Cristina W.,Barbosa, Nilda B. V.,Menezes, Paulo Henrique,Teixeira Da Rocha, Joao Batista,Zeni, Gilson
, p. 5257 - 5268 (2007/10/03)
We present here the reaction of diorganoyl dichalcogenides with terminal alkynes under catalyst-free conditions, by a one-pot procedure, to prepare bis- and tris-chalcogenide alkenes selectively, avoiding the previous preparation of chalcogen alkynes. The reaction proceeded cleanly under mild reaction conditions, and the addition of dichalcogenides to alkynes occurred stereoselectively to give exclusively the corresponding Z isomers. We observed that the selectivity control was governed by the effective participation of the hydroxyl group from propargyl alcohols. In addition, the bis-chalcogenide alkenes were exclusively obtained with propargyl alcohol having the acidic hydroxyl group proton. Conversely, the alkynes with no potentially acidic hydroxyl group proton, at propargyl positons, gave exclusively the tris-chalcogenide alkenes.
New synthetic routes to vinyl sulfides, ketene thioacetals and their seleno analogues from carbonyl compounds
Denis,Desauvage,Hevesi,Krief
, p. 4009 - 4012 (2007/10/02)
Title compounds have been prepared from carbonyl compounds by formal removal of hydroxyl and sulfenyl or hydroxyl and selenyl moieties from the corresponding functionalized β-hydroxysulfides or β-hydroxyselenides.
