476334-33-5 Usage
Uses
Used in Pharmaceutical Synthesis:
(R)-BorohomoPhe-(+)-Pinanediol-HCl is utilized as a chiral auxiliary for the enantioselective reduction of ketones and imines, which is crucial in the production of pharmaceuticals. Its ability to influence the stereochemistry of target molecules ensures the creation of enantiomerically pure compounds, a critical factor in drug efficacy and safety.
Used in Agrochemical Synthesis:
In the agrochemical industry, (R)-BorohomoPhe-(+)-Pinanediol-HCl serves as a chiral auxiliary, aiding in the enantioselective synthesis of active ingredients for pesticides and herbicides. The precise control over stereochemistry provided by this reagent is essential for developing agrochemicals with targeted effects on pests and weeds, minimizing impact on non-target organisms and the environment.
Used in Fine Chemicals Synthesis:
(R)-BorohomoPhe-(+)-Pinanediol-HCl is employed as a chiral auxiliary in the synthesis of fine chemicals, which are high-purity chemicals used in various applications such as fragrances, flavors, dyes, and high-value specialty chemicals. The reagent's capacity to guide the stereoselective reduction of ketones and imines contributes to the production of enantiomerically pure fine chemicals, which is vital for their performance and quality.
Overall, (R)-BorohomoPhe-(+)-Pinanediol-HCl is a valuable asset in the fields of pharmaceuticals, agrochemicals, and fine chemicals, providing a reliable means to achieve the desired stereochemistry in a wide range of chemical syntheses.
Check Digit Verification of cas no
The CAS Registry Mumber 476334-33-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,6,3,3 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 476334-33:
(8*4)+(7*7)+(6*6)+(5*3)+(4*3)+(3*4)+(2*3)+(1*3)=165
165 % 10 = 5
So 476334-33-5 is a valid CAS Registry Number.
476334-33-5Relevant academic research and scientific papers
P1 Phenethyl peptide boronic acid inhibitors of HCV NS3 protease
Priestley,De Lucca, Indawati,Ghavimi, Bahman,Erickson-Viitanen, Susan,Decicco, Carl P.
, p. 3199 - 3202 (2007/10/03)
A series of peptide boronic acids containing extended, hydrophobic P1 residues was prepared to probe the shallow, hydrophobic S1 region of HCV NS3 protease. The p-trifluoromethylphenethyl P1 substituent was identified as optimal with respect to inhibitor potency for NS3 and selectivity against elastase and chymotrypsin.
