54582-01-3 Usage
Description
(R)-(4-hydroxyphenyl)(phenylacetamido)acetic acid is a chiral chemical compound characterized by its molecular structure, which features a phenylacetamido group and a 4-hydroxyphenyl group attached to an acetic acid molecule. (R)-(4-hydroxyphenyl)(phenylacetamido)acetic acid's stereochemistry is denoted as (R), which specifies the configuration of its chiral center. The presence of phenylacetamido and 4-hydroxyphenyl groups, commonly found in various medications and natural compounds, suggests that (R)-(4-hydroxyphenyl)(phenylacetamido)acetic acid may possess pharmacological or biological activities. Further research and analysis are required to ascertain its exact properties and potential applications.
Uses
Used in Pharmaceutical Industry:
(R)-(4-hydroxyphenyl)(phenylacetamido)acetic acid is used as a potential pharmaceutical compound for its possible pharmacological or biological activities. The presence of phenylacetamido and 4-hydroxyphenyl groups, which are known to be active in various medications, indicates that this compound could be a promising candidate for the development of new drugs or therapies.
Used in Research and Development:
In the field of chemical research and development, (R)-(4-hydroxyphenyl)(phenylacetamido)acetic acid serves as a valuable compound for studying its properties, interactions, and potential applications. Its chiral nature and the presence of specific functional groups make it an interesting subject for further investigation, which could lead to the discovery of new chemical reactions, synthesis methods, or applications in various industries.
Used in Chemical Synthesis:
(R)-(4-hydroxyphenyl)(phenylacetamido)acetic acid may be utilized as a building block or intermediate in the synthesis of more complex molecules, particularly in the pharmaceutical, agrochemical, or material science industries. Its unique structure and functional groups could be exploited to create novel compounds with specific properties or applications.
Please note that the specific applications and uses mentioned above are hypothetical and based on the general knowledge of similar chemical structures. The actual applications of (R)-(4-hydroxyphenyl)(phenylacetamido)acetic acid would depend on the results of further research and analysis.
Check Digit Verification of cas no
The CAS Registry Mumber 54582-01-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,8 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 54582-01:
(7*5)+(6*4)+(5*5)+(4*8)+(3*2)+(2*0)+(1*1)=123
123 % 10 = 3
So 54582-01-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H15NO4/c18-13-8-6-12(7-9-13)15(16(20)21)17-14(19)10-11-4-2-1-3-5-11/h1-9,15,18H,10H2,(H,17,19)(H,20,21)/t15-/m1/s1
54582-01-3Relevant articles and documents
One-pot, regioselective synthesis of substituted arylglycines for kinetic resolution by penicillin G acylase
Grundmann, Peter,Fessner, Wolf-Dieter
experimental part, p. 1729 - 1735 (2009/07/24)
Amido-alkylation of electron-rich arenes with phenylacetamide and glyoxylic acid offers an in-expensive route to a large variety of N-phenylacetylated arylglycines that are suited for immediate enzymatic resolution by penicillin G acylase. When performed under mild conditions at 5 °C in acetic acid/HCl, this simple one-pot operation resulted in the formation of single regioisomers only (≥98%). Subsequent kinetic resolution of the amino acid derivatives by penicillin G acylase at pH 8.0 occurred generally with E values >100 and thus furnished free (S)-configurated arylglycines with high enantiomeric purity. The corresponding enantiopure (R)-substrates, easily separable by a phase-selective extraction process, provided the corresponding (R)-enantiomers upon conventional hydrolysis. This one-pot, two-step procedure for arylglycine synthesis, resolution and work-up requires a minimum of equipment and grants rapid access to both enantiopure (S)- and (R)-antipodes of non-natural α-amino acids in small-to large-scale quantities.
