82310-95-0 Usage
Uses
Used in Pharmaceutical Synthesis:
(R)-2-AMINO-4-(4-METHOXY-PHENYL)-BUTYRIC ACID is used as a key building block for the synthesis of various pharmaceuticals and bioactive molecules. Its unique structure allows for the creation of novel compounds with potential therapeutic applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (R)-2-AMINO-4-(4-METHOXY-PHENYL)-BUTYRIC ACID is utilized as a structural component in the design and development of new drugs. Its chiral nature and functional groups make it a versatile candidate for creating molecules with specific biological activities.
Used in Drug Development:
(R)-2-AMINO-4-(4-METHOXY-PHENYL)-BUTYRIC ACID holds promise in drug development due to its potential to be incorporated into molecules with targeted biological effects. Further research into its interactions with biological systems may lead to the discovery of new therapeutic agents.
Used in Research and Development:
(R)-2-AMINO-4-(4-METHOXY-PHENYL)-BUTYRIC ACID is also used in research and development settings to study its structural properties and biological activity. Understanding how (R)-2-AMINO-4-(4-METHOXY-PHENYL)-BUTYRIC ACID interacts with biological targets can provide valuable insights for the development of new pharmaceuticals and therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 82310-95-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,3,1 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 82310-95:
(7*8)+(6*2)+(5*3)+(4*1)+(3*0)+(2*9)+(1*5)=110
110 % 10 = 0
So 82310-95-0 is a valid CAS Registry Number.
82310-95-0Relevant academic research and scientific papers
PREPARATION OF HOMOLOGS OF L-2-AMINO-5-(p-METOXYPHENYL)PENTANOIC ACID
Kosui, Nobuo,Waki, Michinori,Kato, Tetsuo,Izumiya, Nobuo
, p. 918 - 920 (2007/10/02)
Lower and higher homologs, L-2-amino-4-(p-methoxyphenyl)butanoic acid (L-amb) and L-2-amino-6-(p-methoxyphenyl)hexanoic acid (L-Amh), of L-2-amino-5-(p-methoxyphenyl)pentanoic acid were prepared by optical resolution of N-acetyl-DL-Amb and of N-acetyl-DL-Amh with Aspergillus acylase.N-acetyl DL-Amb or N-acetyl-DL-Amh was synthesized from (acetamido malonic acid by heating with p-xylene.
