145238-45-5 Usage
Description
(R)-Tetrahydro-1,3,3-triphenyl-1H,3H-pyrrolo[1,2-c][1,3,2]oxaborole, 99% (R)-Phenyl oxazaborolidine is a complex organic compound with a unique structure that features a tetrahydro-1,3,3-triphenyl-1H,3H-pyrrolo[1,2-c][1,3,2]oxaborole core and a phenyl oxazaborolidine group. (R)-Tetrahydro-1,3,3-triphenyl-1H,3H-pyrrolo[1,2-c][1,3,2]oxaborole, 99% (R)-Phenyl oxazaborolidine is characterized by its high purity (99%) and is known for its ability to act as a catalyst in various chemical reactions.
Uses
Used in Pharmaceutical Industry:
(R)-Tetrahydro-1,3,3-triphenyl-1H,3H-pyrrolo[1,2-c][1,3,2]oxaborole, 99% (R)-Phenyl oxazaborolidine is used as a convenient catalyst for the enantioselective borane reduction of ketones at ambient temperatures. This application is particularly important in the pharmaceutical industry, where the synthesis of chiral drugs with high enantiomeric purity is crucial. The use of this compound as a catalyst allows for the selective reduction of ketones to form chiral alcohols, which can be further utilized in the development of various pharmaceutical products.
Used in Chemical Synthesis:
In the field of chemical synthesis, (R)-Tetrahydro-1,3,3-triphenyl-1H,3H-pyrrolo[1,2-c][1,3,2]oxaborole, 99% (R)-Phenyl oxazaborolidine serves as a valuable catalyst for enantioselective borane reduction reactions. This enables chemists to synthesize a wide range of chiral compounds with high enantiomeric purity, which are essential for various applications, including the development of new drugs, agrochemicals, and other specialty chemicals.
Used in Research and Development:
(R)-Tetrahydro-1,3,3-triphenyl-1H,3H-pyrrolo[1,2-c][1,3,2]oxaborole, 99% (R)-Phenyl oxazaborolidine is also utilized in research and development laboratories for the study of enantioselective catalysis and the development of new synthetic methods. Its high purity and catalytic efficiency make it an ideal candidate for exploring the potential of enantioselective borane reduction in various chemical transformations, leading to the discovery of novel compounds and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 145238-45-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,2,3 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 145238-45:
(8*1)+(7*4)+(6*5)+(5*2)+(4*3)+(3*8)+(2*4)+(1*5)=125
125 % 10 = 5
So 145238-45-5 is a valid CAS Registry Number.
145238-45-5Relevant articles and documents
PROCESS TO MAKE A SELECTIVE CATHEPSIN CYSTEINE PROTEASE INHIBITOR
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Page/Page column 20-21, (2020/02/23)
A method of preparing a compound of Formula (I) comprising reacting the compound of Formula (A) with a base and a compound of Formula (B) to yield a compound of Formula (C).