46988-94-7 Usage
Uses
Used in Pharmaceutical Industry:
(2S)-(+)-N-tert-Butoxycarbonyl-2-(3-hydroxyphenyl)glycine is used as a building block for the preparation of various peptides and peptidomimetics. Its unique structure and properties make it valuable for the development of pharmaceuticals and bioactive compounds.
Used in Organic Synthesis:
(2S)-(+)-N-tert-Butoxycarbonyl-2-(3-hydroxyphenyl)glycine is used as a key intermediate in organic synthesis, enabling the creation of complex organic molecules and compounds.
Used in Enantioselective Synthesis:
(2S)-(+)-N-tert-Butoxycarbonyl-2-(3-hydroxyphenyl)glycine is used as a chiral building block for enantioselective synthesis in the pharmaceutical industry and academic research, allowing for the creation of enantiomerically pure compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 46988-94-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,9,8 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 46988-94:
(7*4)+(6*6)+(5*9)+(4*8)+(3*8)+(2*9)+(1*4)=187
187 % 10 = 7
So 46988-94-7 is a valid CAS Registry Number.
46988-94-7Relevant academic research and scientific papers
Nonproteinogenic Amino Acids, IV. - EPC Synthesis of L-(+)-Forphenicine
Weinges, Klaus,Reinel, Ute,Maurer, Wolfgang,Gaessler, Norbert
, p. 833 - 838 (2007/10/02)
Enantiomerically pure L-(+)-forphenicine (12) is synthesized starting from purchasable 3-methoxybenzaldehyde (1) by the use of (4S,5S)-(+)-5-amino-2,2-dimethyl-4-phenyl-1,3-dioxane (2) as a chiral auxiliary and prussic acid. 12 is identical with the natural product which has been isolated from the culture broth of an Actinomyces species and which is known to be a potent inhibitor of alkaline phosphatase.
