222842-90-2 Usage
Description
(S)-2-amino-3-(4-(2-tert-butoxy-2-oxoethyl)phenyl)propanoic acid is a chiral chemical compound derived from propanoic acid, featuring an amino group at the second position, a 3-carbon propanoic acid chain, and a phenyl group with a tert-butoxy and oxoethyl substituent at the 4-position. This molecule is of interest in organic synthesis and pharmaceutical research due to its potential bioactivity, making it a promising candidate for the development of new medicines and biologically active compounds.
Uses
Used in Pharmaceutical Research:
(S)-2-amino-3-(4-(2-tert-butoxy-2-oxoethyl)phenyl)propanoic acid is used as a key intermediate in the synthesis of various pharmaceutical compounds for [application reason]. Its unique structure and chirality allow for the creation of novel drugs with specific therapeutic targets.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-2-amino-3-(4-(2-tert-butoxy-2-oxoethyl)phenyl)propanoic acid is used as a building block for the development of complex molecular structures with potential applications in material science, chemical engineering, and other related industries.
Used in Drug Development:
(S)-2-amino-3-(4-(2-tert-butoxy-2-oxoethyl)phenyl)propanoic acid is utilized as a starting material for the design and synthesis of new drugs, particularly those targeting specific biological pathways or receptors. Its chiral nature enables the creation of enantiomer-specific pharmaceuticals, which can have different effects on the body.
Used in the Development of Biologically Active Compounds:
(S)-2-amino-3-(4-(2-tert-butoxy-2-oxoethyl)phenyl)propanoic acid is also used in the creation of biologically active molecules, which can interact with biological systems to produce a desired effect. The potential applications of these compounds span across various therapeutic areas, including but not limited to, cardiovascular, neurological, and anti-inflammatory treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 222842-90-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,2,8,4 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 222842-90:
(8*2)+(7*2)+(6*2)+(5*8)+(4*4)+(3*2)+(2*9)+(1*0)=122
122 % 10 = 2
So 222842-90-2 is a valid CAS Registry Number.
222842-90-2Relevant articles and documents
Synthesis of Fmoc-protected 4-carboxydifluoromethyl-L-phenylalanine: A phosphotyrosyl mimetic of potential use for signal transduction studies
Yao, Zhu-Jun,Gao, Yang,Voigt, Johannes H.,Ford Jr., Harry,Burke Jr., Terrence R.
, p. 2865 - 2874 (2007/10/03)
4-(Carboxymethyl)phenylalanine (2) and its α,α-difluoro homologue 4- (carboxydifluoromethyl)-phenylalanine (3) have been described as phosphotyrosyl mimetics. Herein we report the synthesis of N-Fmoc 4-(O-tert- butyl carboxymethyl)phenylalanine (4) and N-
