62023-61-4 Usage
Description
(2R,3R)-3-AMINO-2-HYDROXY-4-PHENYL-BUTYRIC ACID is a chemical compound with the molecular formula C10H13NO3. It is an amino acid derivative characterized by its specific (2R,3R) stereochemistry. (2R,3R)-3-AMINO-2-HYDROXY-4-PHENYL-BUTYRIC ACID features an amino group, a hydroxy group, and a phenyl group, which contribute to its versatility in organic chemistry and biochemistry. Due to its structural similarity to naturally occurring amino acids, it may possess potential biological activity and can be utilized as a precursor in the synthesis of pharmaceuticals, agrochemicals, or other fine chemicals. (2R,3R)-3-AMINO-2-HYDROXY-4-PHENYL-BUTYRIC ACID's specific properties and applications are contingent upon its purity, stereochemistry, and the context of its use in chemical or biochemical research and development.
Uses
Used in Pharmaceutical Industry:
(2R,3R)-3-AMINO-2-HYDROXY-4-PHENYL-BUTYRIC ACID is used as a precursor in the synthesis of pharmaceuticals for its potential biological activity and structural resemblance to naturally occurring amino acids. This allows for the development of new drugs with specific therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical industry, (2R,3R)-3-AMINO-2-HYDROXY-4-PHENYL-BUTYRIC ACID is used as a building block in the creation of agrochemicals, potentially leading to the development of novel pesticides or other agricultural products that can enhance crop protection and yield.
Used in Fine Chemicals Synthesis:
(2R,3R)-3-AMINO-2-HYDROXY-4-PHENYL-BUTYRIC ACID serves as a versatile intermediate in the synthesis of fine chemicals, which are high-purity, specialty chemicals used in various industries such as fragrances, flavors, and cosmetics. Its unique functional groups and stereochemistry make it a valuable component in the production of these high-value compounds.
Used in Chemical Research and Development:
(2R,3R)-3-AMINO-2-HYDROXY-4-PHENYL-BUTYRIC ACID is utilized in chemical research and development for exploring its potential applications and properties. Its unique structure and stereochemistry make it an interesting subject for studies aimed at understanding its reactivity, stability, and interactions with other molecules, which can lead to new discoveries and applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 62023-61-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,2 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62023-61:
(7*6)+(6*2)+(5*0)+(4*2)+(3*3)+(2*6)+(1*1)=84
84 % 10 = 4
So 62023-61-4 is a valid CAS Registry Number.
62023-61-4Relevant articles and documents
N -Boc amines to oxazolidinones via Pd(II)/bis-sulfoxide/br?nsted acid Co-catalyzed allylic C-H oxidation
Osberger, Thomas J.,White, M. Christina
, p. 11176 - 11181 (2014/08/18)
A Pd(II)/bis-sulfoxide/Br?nsted acid catalyzed allylic C-H oxidation reaction for the synthesis of oxazolidinones from simple N-Boc amines is reported. A range of oxazolidinones are furnished in good yields (avg 63%) and excellent diastereoselectivities (avg 15:1) to furnish products regioisomeric from those previously obtained using allylic C-H amination reactions. Mechanistic studies suggest the role of the phosphoric acid is to furnish a Pd(II)bis-sulfoxide phosphate catalyst that promotes allylic C-H cleavage and π-allylPd functionalization with a weak, aprotic oxygen nucleophile and to assist in catalyst regeneration.
Regio- and stereo-specific synthesis of threo-3-amino-2-hydroxy-acids, novel amino-acids contained in aminopeptidase inhibitors of microbial origin.
Kato,Saino,Nishizawa,Takita,Umezawa
, p. 1618 - 1621 (2007/10/02)
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