5925-75-7 Usage
Description
METHYL THIOPROPIONATE is an organic compound with the chemical formula C4H8OS. It is a colorless liquid with a fruity, milk-like aroma. METHYL THIOPROPIONATE is known for its various applications across different industries due to its unique properties.
Uses
Used in Flavor and Fragrance Industry:
METHYL THIOPROPIONATE is used as a flavoring agent for its fruity, milk-like aroma, adding a pleasant taste and scent to various products in the food and beverage industry.
Used in Chemical Synthesis:
METHYL THIOPROPIONATE serves as an important intermediate in the synthesis of various chemicals, including pharmaceuticals and agrochemicals, due to its reactive thiol group.
Used in the Production of Plasticizers:
METHYL THIOPROPIONATE is used as a raw material in the production of plasticizers, which are additives that increase the flexibility and workability of plastics.
Used in the Rubber Industry:
METHYL THIOPROPIONATE is utilized as an additive in the rubber industry to enhance the properties of rubber, such as its flexibility and durability.
Used in the Pharmaceutical Industry:
METHYL THIOPROPIONATE is employed as a starting material for the synthesis of various pharmaceutical compounds, contributing to the development of new drugs and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 5925-75-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,2 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5925-75:
(6*5)+(5*9)+(4*2)+(3*5)+(2*7)+(1*5)=117
117 % 10 = 7
So 5925-75-7 is a valid CAS Registry Number.
InChI:InChI=1S/C4H8OS/c1-3-4(5)6-2/h3H2,1-2H3
5925-75-7Relevant articles and documents
Processes for preparing carbapenem derivatives
-
, (2008/06/13)
The invention relates to carbapenem derivatives useful as antimicrobial agents, more particularly to intermediate compounds for the preparations thereof of the formula STR1
Acid-Catalyzed Hydrolysis of Ketene Dithioacetals and Trithioorthocarboxylates. Effect of β-Methyl Substitution
Okuyama, Tadashi,Kawao, Shoji,Fueno, Takayuki
, p. 85 - 88 (2007/10/02)
Hydrolysis rates of β-methyl-substituted ketene dithioacetals were measured. β-Monomethyl and β,β-dimethyl substitutions reduced the reactivity of the parent acetal by factors of 26 and 6.7 x 105, respectively.Similar methyl substitutions of trithioorthoacetate, however, enhanced the hydrolysis reactivity by 3 and 23 times.The reversibility of protonation of ketene dithioacetal during hydrolysis was slightly increased by a β-methyl group, but dimethyl substitution seemed to inhibit reversibility by raising the potential barrier to protonation.
ACTION DE L'OZONE SUR DES DERIVES VINYLIQUES; REACTIONS CONSERVANT L'ENCHAINEMENT CARBONE.
Strobel, Marie-Paule,Morin, Luc,Paquer, Daniel
, p. 523 - 524 (2007/10/02)
Ozone reacts with vinyl derivatives (sulphides, enamines, ethers) and gives abnormal reactions or/and double bond cleavages.