88455-08-7 Usage
Description
(2S)-3-methyl-2-[[(2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl]amino]buta noic acid, also known as 3-methylthreonine, is a naturally occurring amino acid and a key building block of proteins. It is classified as a beta-amino acid due to the presence of an additional carbon atom between the alpha and beta carbons. This unique chemical structure and functional properties make it an essential component of the biochemical pathways that support life, playing a crucial role in the biosynthesis of various peptides and proteins, contributing to the structural and functional diversity of biological molecules.
Uses
Used in Pharmaceutical Industry:
(2S)-3-methyl-2-[[(2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl]amino]buta noic acid is used as a key building block for the development of new pharmaceutical compounds. Its unique structure and functional properties make it a promising candidate for the design and synthesis of novel drugs with improved therapeutic effects.
Used in Biochemical Research:
(2S)-3-methyl-2-[[(2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl]amino]buta noic acid is used as a research tool in biochemical studies. Its unique chemical structure allows scientists to investigate the role of beta-amino acids in the biosynthesis of peptides and proteins, as well as their contribution to the structural and functional diversity of biological molecules.
Used in Nutritional Supplements:
(2S)-3-methyl-2-[[(2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl]amino]buta noic acid is used as an ingredient in nutritional supplements. Its role in the biosynthesis of peptides and proteins can support the maintenance of healthy bodily functions and contribute to overall well-being.
Used in Cosmetics Industry:
(2S)-3-methyl-2-[[(2S,3R,4R,5R)-2,3,4,5,6-pentahydroxyhexyl]amino]buta noic acid is used as an active ingredient in cosmetics. Its unique properties can contribute to the development of innovative skincare and beauty products with enhanced efficacy and benefits for the users.
Check Digit Verification of cas no
The CAS Registry Mumber 88455-08-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,4,5 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 88455-08:
(7*8)+(6*8)+(5*4)+(4*5)+(3*5)+(2*0)+(1*8)=167
167 % 10 = 7
So 88455-08-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H23NO7/c1-5(2)8(11(18)19)12-3-6(14)9(16)10(17)7(15)4-13/h5-10,12-17H,3-4H2,1-2H3,(H,18,19)/t6-,7+,8-,9+,10+/m0/s1
88455-08-7Relevant articles and documents
SYNTHETIC ROUTES TO N-(1-DEOXY-D-FRUCTOS-1-YL)AMINO ACIDS BY WAY OF REDUCTIVE AMINATION OF HEXOS-2-ULOSES
Walton, Donald J.,McPherson, John D.
, p. 123 - 130 (2007/10/02)
There are described two routes to the synthesis of N-(1-deoxy-D-fructos-1-yl) derivatives of L-valine, L-leucine, L-methionine, L-phenylalanine, and 6-aminohexanoic acid.One route involved reductive amination of D-arabino-hexos-2-ulose in the presence of
