32298-34-3 Usage
Description
2-[(2-methoxyphenyl)methyl]butanedioic acid, also known as Methoxyphenyl Acetone or MPA, is an organic compound with a molecular formula C12H14O4. It is a white, crystalline solid that serves as a versatile precursor in the synthesis of various pharmaceuticals and agrochemicals. As a chiral compound, MPA possesses two enantiomers, each with distinct properties and applications. It is a common reagent in organic chemistry and is utilized as a building block in the synthesis of a wide range of organic compounds. MPA is also recognized for its role as a precursor in the development of novel drugs and its involvement in numerous chemical reactions.
Uses
Used in Pharmaceutical Industry:
2-[(2-methoxyphenyl)methyl]butanedioic acid is used as a precursor in the synthesis of various pharmaceuticals for its ability to contribute to the development of novel drugs with potential therapeutic applications.
Used in Agrochemical Industry:
2-[(2-methoxyphenyl)methyl]butanedioic acid is used as a precursor in the synthesis of agrochemicals to develop new compounds that can enhance crop protection and yield.
Used in Organic Chemistry:
2-[(2-methoxyphenyl)methyl]butanedioic acid is used as a common reagent in organic chemistry for its role in the synthesis of various organic compounds, contributing to the advancement of chemical research and development.
Used in Chiral Compounds Research:
2-[(2-methoxyphenyl)methyl]butanedioic acid, as a chiral compound with two distinct enantiomers, is used in research to explore the different properties and applications of each enantiomer, furthering the understanding of stereochemistry and its impact on chemical reactions and biological activity.
Check Digit Verification of cas no
The CAS Registry Mumber 32298-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,2,9 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 32298-34:
(7*3)+(6*2)+(5*2)+(4*9)+(3*8)+(2*3)+(1*4)=113
113 % 10 = 3
So 32298-34-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O5/c1-17-10-5-3-2-4-8(10)6-9(12(15)16)7-11(13)14/h2-5,9H,6-7H2,1H3,(H,13,14)(H,15,16)
32298-34-3Relevant articles and documents
Benzoxaborole antimalarial agents. Part 2: Discovery of fluoro-substituted 7-(2-carboxyethyl)-1,3-dihydro-1-hydroxy-2,1-benzoxaboroles
Zhang, Yong-Kang,Plattner, Jacob J.,Freund, Yvonne R.,Easom, Eric E.,Zhou, Yasheen,Ye, Long,Zhou, Huchen,Waterson, David,Gamo, Francisco-Javier,Sanz, Laura M.,Ge, Min,Li, Zhiya,Li, Lingchao,Wang, Hailong,Cui, Han
, p. 1299 - 1307 (2012/03/26)
A series of new boron-containing benzoxaborole compounds was designed and synthesized for a continuing structure-activity relationship (SAR) investigation to assess the antimalarial activity changes derived from side-chain structural variation, substituent modification on the benzene ring and removal of boron from five-membered oxaborole ring. This SAR study demonstrated that boron is required for the antimalarial activity, and discovered that three fluoro-substituted 7-(2-carboxyethyl)-1,3-dihydro-1-hydroxy-2,1-benzoxaboroles (9, 14 and 20) have excellent potencies (IC50 0.026-0.209 μM) against Plasmodium falciparum.
