25333-24-8 Usage
Description
METHYL 3-BENZOYLPROPIONATE, also known as Methyl 3-(phenylcarbonyl)propanoate, is an organic compound that serves as a chemical and organic intermediate. It is a clear colorless to yellow liquid with unique chemical properties that make it suitable for various applications across different industries.
Uses
Used in Chemical Industry:
METHYL 3-BENZOYLPROPIONATE is used as a chemical intermediate for the synthesis of various compounds and materials. Its chemical structure allows it to be a versatile building block in the creation of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
METHYL 3-BENZOYLPROPIONATE is used as an organic intermediate in the development of new drugs and pharmaceutical compounds. Its unique properties enable it to be a key component in the synthesis of novel therapeutic agents, potentially contributing to the advancement of medical treatments.
Used in Agrochemical Industry:
METHYL 3-BENZOYLPROPIONATE is used as an organic intermediate in the formulation of agrochemicals, such as pesticides and herbicides. Its role in these products helps to improve the efficiency and effectiveness of these chemicals in agricultural applications.
Used in Specialty Chemicals Industry:
METHYL 3-BENZOYLPROPIONATE is used as a chemical intermediate in the production of specialty chemicals, which are tailored to meet specific requirements in various industries, such as cosmetics, coatings, and plastics. Its unique properties make it a valuable component in the development of these specialized products.
Check Digit Verification of cas no
The CAS Registry Mumber 25333-24-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,3 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 25333-24:
(7*2)+(6*5)+(5*3)+(4*3)+(3*3)+(2*2)+(1*4)=88
88 % 10 = 8
So 25333-24-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O3/c1-14-11(13)8-7-10(12)9-5-3-2-4-6-9/h2-6H,7-8H2,1H3
25333-24-8Relevant articles and documents
3,6-bis(triphenylphosphonium)cyclohexene peroxodisulfate: A highly efficient oxidant for the selective oxidation of benzylic alcohols
Badri,Shalbaf,Heidary
, p. 3473 - 3479 (2001)
The synthesis of 3,6-bis(triphenylphosphonium)cyclohexene peroxodisulfate and its application for the selective oxidation of benzylic alcohols is reported.
Tandem homologation-acylation chemistry: Single and double homologation
Henderson, Carley S.,Mazzone, Jennifer R.,Moore, Amanda M.,Zercher, Charles K.
supporting information, (2021/06/01)
Treatment of β-dicarbonyls with the Furakawa-variant of the Simmons-Smith reagent results in homologation and production of an intermediate zinc enolate. Treatment of the enolate with various acylating agents generate products with both γ-dicarbonyl funct
LIGHT INDUCED CATALYTIC C-H OXYGENATION OF ALKANES
-
Paragraph 00219, (2021/04/02)
A method of oxygenating a benzylic C-H bond is provided. The method comprises light induced activation of an initiator and subsequent reaction with oxygen, resulting in the formation of free radicals. Subsequently, free radicals catalyze the reaction of the benzylic C-H bond with oxygen, thereby forming an oxygenated compound.
Metal-free reduction of unsaturated carbonyls, quinones, and pyridinium salts with tetrahydroxydiboron/water
Li, Tiejun,Peng, Henian,Tang, Wenjun,Tian, Duanshuai,Xu, Guangqing,Yang, He
, p. 4327 - 4337 (2021/05/31)
A series of unsaturated carbonyls, quinones, and pyridinium salts have been effectively reduced to the corresponding saturated carbonyls, dihydroxybenzenes, and hydropyridines in moderate to high yields with tetrahydroxydiboron/water as a mild, convenient, and metal-free reduction system. Deuterium-labeling experiments have revealed this protocol to be an exclusive transfer hydrogenation process from water. This journal is