457654-75-0 Usage
Uses
Used in Pharmaceutical Industry:
(R)-3-chlorophenylalanine methyl ester hydrochloride is used as a building block for the synthesis of peptides and biologically active compounds. The presence of the chlorophenyl group allows for the modulation of properties and activities of peptides and proteins, which can be crucial in the development of new drugs and therapies.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (R)-3-chlorophenylalanine methyl ester hydrochloride is used as a research tool to study the effects of the chlorophenyl group on the properties and activities of peptides and proteins. This can lead to a better understanding of molecular interactions and the development of more effective drugs.
Used in Laboratory Settings:
The hydrochloride salt form of (R)-3-chlorophenylalanine methyl ester hydrochloride increases its water solubility and stability, making it easier to handle and utilize in laboratory settings. This enhances the compound's practicality for various research and development applications.
Check Digit Verification of cas no
The CAS Registry Mumber 457654-75-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,7,6,5 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 457654-75:
(8*4)+(7*5)+(6*7)+(5*6)+(4*5)+(3*4)+(2*7)+(1*5)=190
190 % 10 = 0
So 457654-75-0 is a valid CAS Registry Number.
457654-75-0Relevant articles and documents
A diastereoselective construction of pyrazinoisoquinoline skeletons via tandem cyclization of phenylalanine derivatives: A facile synthesis of optically active pyrazinoisoquinolines
Seki, Maki,Ogiku, Tsuyoshi
, p. 3864 - 3870 (2014/06/09)
A facile and stereocontrolled construction of optically active pyrazinoisoquinoline skeletons based on tandem cyclization of enantiopure phenylalanine derivatives was examined. The reaction provided optically active 6,11b-trans pyrazinoisoquinoline ring systems in excellent diastereoselectivity, and this method was applicable to the cyclization of phenylalanine derivatives with diverse substituents.
