233665-96-8 Usage
Description
ETHYL 3-(METHYLTHIO)BUTYRATE is an organic compound with a sulfury odor and a mild sulfurous taste with tropical overripe fruity pulpy notes, vegetative, and cheesy nuances. It is characterized by its aroma threshold values, with a detection level at 19 ppb and a 1.0% solution exhibiting tropical fruity, red fruit, pineapple, and earthy, fatty, and waxy nuances.
Uses
Used in Flavor Industry:
ETHYL 3-(METHYLTHIO)BUTYRATE is used as a flavoring agent for its unique tropical fruity, red fruit, and pineapple aroma with sulfurous, earthy, fatty, and waxy nuances. It is particularly suitable for enhancing the taste and aroma of various food and beverage products.
Used in Fragrance Industry:
ETHYL 3-(METHYLTHIO)BUTYRATE is used as a fragrance ingredient for its mild sulfurous and tropical overripe fruity pulpy notes, as well as its vegetative and cheesy nuances. It can be employed in the creation of various perfumes, colognes, and other scented products to provide a distinct and appealing aroma profile.
Used in Chemical Research:
ETHYL 3-(METHYLTHIO)BUTYRATE can be utilized as a research compound in the field of organic chemistry, particularly for studying its chemical properties, reactivity, and potential applications in the synthesis of other compounds or materials.
Check Digit Verification of cas no
The CAS Registry Mumber 233665-96-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,3,6,6 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 233665-96:
(8*2)+(7*3)+(6*3)+(5*6)+(4*6)+(3*5)+(2*9)+(1*6)=148
148 % 10 = 8
So 233665-96-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O2S/c1-4-9-7(8)5-6(2)10-3/h6H,4-5H2,1-3H3
233665-96-8Relevant articles and documents
A facile generation of C-S bonds via one-pot, odourless and efficient thia-Michael addition reactions using alkyl, aryl or allyl halides, thiourea and electron-deficient alkenes in wet polyethylene glycol (PEG 200) under mild reaction conditions
Firouzabadi, Habib,Iranpoor, Nasser,Abbasi, Mohammad
experimental part, p. 5293 - 5301 (2009/11/30)
An efficient and odourless synthesis of thia-Michael adducts by the reaction of various organic halides (primary, secondary, tertiary, allylic, and benzylic), structurally diverse electron-deficient alkenes (ketones, esters, and acrylonitrile) and thioure
