19112-35-7 Usage
Description
3-(2-CHLORO-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER is an organic compound that serves as a versatile intermediate in the synthesis of various chemical products. It is characterized by its ester functional group and a chlorophenyl moiety, which contribute to its reactivity and potential applications in different industries.
Uses
Used in Pharmaceutical Industry:
3-(2-CHLORO-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER is used as a reactant for the preparation of diaryl-substituted pyrazoles, which are potent CCR2 receptor antagonists. These antagonists have potential applications in the treatment of various inflammatory and autoimmune diseases, such as rheumatoid arthritis and multiple sclerosis.
Used in Chemical Synthesis:
3-(2-CHLORO-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER is used as a reactant in cerium ammonium nitrate-mediated oxidative coupling reactions. This process allows for the formation of new carbon-carbon bonds, which are essential in the synthesis of complex organic molecules.
Used in Hydrosilylation Reactions:
In the field of organometallic chemistry, 3-(2-CHLORO-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER is used as a reactant in hydrosilylation reactions. These reactions involve the addition of a silicon-hydrogen bond to an unsaturated carbon-carbon bond, leading to the formation of new organic compounds with potential applications in various industries.
Used in Agrochemical Industry:
3-(2-CHLORO-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER is used as a reactant in the preparation of potential herbicidal agents. These agents are designed to control the growth of unwanted plants in agricultural fields, thereby increasing crop yield and reducing the need for manual labor.
Used in Asymmetric Catalysis:
3-(2-CHLORO-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER is used as a reactant in ruthenium-catalyzed asymmetric hydrogenation reactions. This process allows for the selective reduction of prochiral compounds, leading to the formation of enantiomerically pure products. These products have potential applications in the synthesis of chiral pharmaceuticals and other specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 19112-35-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,1 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19112-35:
(7*1)+(6*9)+(5*1)+(4*1)+(3*2)+(2*3)+(1*5)=87
87 % 10 = 7
So 19112-35-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H11ClO3/c1-2-15-11(14)7-10(13)8-5-3-4-6-9(8)12/h3-6H,2,7H2,1H3
19112-35-7Relevant articles and documents
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Wierenga,W.,Skulnick,H.I.
, p. 310 - 311 (1979)
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Double Enzyme-Catalyzed One-Pot Synthesis of Enantiocomplementary Vicinal Fluoro Alcohols
Fan, Jiajie,Lin, Xianfu,Peng, Yongzhen,Wang, Anlin,Wu, Qi,Xu, Jian,Xu, Weihua,Yu, Huilei
supporting information, (2020/07/24)
A double-enzyme-catalyzed strategy for the synthesis of enantiocomplementary vicinal fluoro alcohols through a one-pot, three-step process including lipase-catalyzed hydrolysis, spontaneous decarboxylative fluorination, and subsequent ketoreductase-catalyzed reduction was developed. With this approach, β-ketonic esters were converted to the corresponding vicinal fluoro alcohols with high isolated yields (up to 92percent) and stereoselectivities (up to 99percent). This new cascade process addresses some issues in comparison with traditional methods such as environmentally hazardous reaction conditions and low stereoselectivity outcome.
Tetrazolinone compound and application for same
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Paragraph 0675; 0676; 0677; 0678, (2016/10/08)
Provided is a tetrazolinone compound given by formula (1) (wherein E represents a 5-membered aromatic hetero group, such as the pyrazolyl group, the thiazolyl group, or the imidazolyl group; R4 and R5 represent hydrogen atoms or the like; R6 represents a C1-12 alkyl group; R7, R8, and R9 represent hydrogen atoms or the like; R10 represents a C1-3 alkyl group, or a C1-3 haloalkyl group; Y represents an oxygen atom or the like; and Q represents an oxygen atom or the like), and having exceptional efficacy in controlling harmful organisms.