1223573-30-5 Usage
Description
Ethyl 2-(thietan-3-ylidene)acetate, also known as ethyl 3-thietanecarboxylate, is a chemical compound with the molecular formula C7H10O2S. It is classified as an ester and is known for its fruity and sulfurous aroma. Ethyl 2-(thietan-3-ylidene)acetate can be found in various fruits and vegetables and is commonly used in the fragrance and flavor industry.
Uses
Used in Fragrance Industry:
Ethyl 2-(thietan-3-ylidene)acetate is used as a fragrance ingredient for its tropical or citrusy scent. It is added to perfumes to impart a refreshing and fruity aroma, enhancing the overall scent profile.
Used in Flavor Industry:
In the flavor industry, Ethyl 2-(thietan-3-ylidene)acetate is used as a flavoring agent to provide a fruity and sulfurous taste to food products. It is commonly added to beverages, candies, and other food items to enhance their flavor and create a unique taste experience.
Used in Consumer Product Production:
Ethyl 2-(thietan-3-ylidene)acetate is considered safe for use in various consumer products, including perfumes and food items. Its wide usage in the production of these products is due to its ability to impart a pleasant aroma and taste, making it a popular choice in the industry.
Check Digit Verification of cas no
The CAS Registry Mumber 1223573-30-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,3,5,7 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1223573-30:
(9*1)+(8*2)+(7*2)+(6*3)+(5*5)+(4*7)+(3*3)+(2*3)+(1*0)=125
125 % 10 = 5
So 1223573-30-5 is a valid CAS Registry Number.
1223573-30-5Relevant articles and documents
Synthesis of 6-Azaspiro[4.3]alkanes: Innovative Scaffolds for Drug Discovery
Chalyk, Bohdan A.,Isakov, Andrei A.,Butko, Maryna V.,Hrebeniuk, Kateryna V.,Savych, Olena V.,Kucher, Olexandr V.,Gavrilenko, Konstantin S.,Druzhenko, Tetiana V.,Yarmolchuk, Vladimir S.,Zozulya, Sergey,Mykhailiuk, Pavel K.
, p. 4530 - 4542 (2017/08/30)
New scaffolds for drug discovery, 6-azaspiro[4.3]alkanes, have been synthesized in two steps from four-membered-ring ketones: cyclobutanone, thienone, N-Boc-azetidinone (Boc = tert-butoxycarbonyl), etc. The key transformation was the reaction between electron-deficient exocyclic alkenes and an in-situ generated N-benzylazomethine ylide.
AZA-OXO-INDOLES FOR THE TREATMENT AND PROPHYLAXIS OF RESPIRATORY SYNCYTIAL VIRUS INFECTION
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Page/Page column 119, (2014/12/12)
The invention provides compounds having the general formula: wherein R1, R2, R3, R4, R5, R6, W1, W2, W3, A and X are as described herein, compositions including the compounds and methods of using the compounds.