245323-38-0 Usage
Description
(S)-4-TERT-BUTOXY-4-OXO-2-PHENYLBUTANOIC ACID, with the molecular formula C16H20O4, is a carboxylic acid derivative and a member of the phenylbutanoic acids class within organic compounds. As an enantiomer of 4-tert-butoxy-4-oxo-2-phenylbutanoic acid, it holds potential for applications in both the pharmaceutical and agricultural sectors, possibly serving as a precursor in the synthesis of biologically active molecules or as an intermediate in agrochemical production.
Uses
Used in Pharmaceutical Industry:
(S)-4-TERT-BUTOXY-4-OXO-2-PHENYLBUTANOIC ACID is used as a building block for the synthesis of biologically active molecules due to its unique chemical structure and properties, which may contribute to the development of new pharmaceutical agents.
Used in Agricultural Industry:
(S)-4-TERT-BUTOXY-4-OXO-2-PHENYLBUTANOIC ACID is used as an intermediate in the production of agrochemicals, potentially enhancing the effectiveness of these products and contributing to advancements in agricultural technology.
However, it is important to note that further research is required to fully explore and understand the potential applications and effects of (S)-4-TERT-BUTOXY-4-OXO-2-PHENYLBUTANOIC ACID in these industries.
Check Digit Verification of cas no
The CAS Registry Mumber 245323-38-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,5,3,2 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 245323-38:
(8*2)+(7*4)+(6*5)+(5*3)+(4*2)+(3*3)+(2*3)+(1*8)=120
120 % 10 = 0
So 245323-38-0 is a valid CAS Registry Number.
245323-38-0Relevant articles and documents
Preparation of chiral 3-arylpyrrolidines via the enantioselective 1,4-addition of arylboronic acids to fumaric esters catalyzed by Rh(I)/chiral diene complexes
Chung, Yu-Chiang,Janmanchi, Damodar,Wu, Hsyueh-Liang
, p. 2766 - 2769 (2012/07/17)
A highly efficient rhodium-catalyzed protocol for the preparation of 2-arylsuccinic esters and 3-arylpyrrolidines of high optical purity has been achieved. In the presence of 1 mol % of a chiral diene/Rh(I) catalyst, asymmetric addition of various arylbor
A general method for the synthesis of enantiomerically pure β- substituted, β-amino acids through α-substituted succinic acid derivatives
Evans, David A.,Wu, Leester D.,Wiener, John J. M.,Johnson, Jeffrey S.,Ripin, David H. B.,Tedrow, Jason S.
, p. 6411 - 6417 (2007/10/03)
A general procedure for the synthesis of enantiopure β-substituted, β- amino acids is presented. Alkylation of the sodium enolates derived from chiral N-acyloxazolidinone imides 2 (R = Me, i-Pr, t-Bu, Ph, Bn) with tert- butyl bromoacetate afforded the 2-substituted succinate derivatives 3 in good yields (82-89%) and with high selectivity (≥ 93;7). Following hydrolysis, Curtius rearrangement of the resulting carboxylic acid provided the enantiopure benzyloxycarbonyl (Cbz)-protected β-amino esters 6 in good yields (74-79%).
