62234-37-1 Usage
Description
CBZ-BETA-AMINO-D-ALANINE, also known as Nalpha-Benzyloxycarbonyl-D-2,3-diaminopropionic Acid, is a chemical compound with the chemical properties of a white to light yellow crystal powder. It is a derivative of amino acids and has potential applications in various industries due to its unique structure and properties.
Uses
Used in Pharmaceutical Industry:
CBZ-BETA-AMINO-D-ALANINE is used as an intermediate in the synthesis of various pharmaceutical compounds for [application reason]. Its unique structure allows it to be a key component in the development of new drugs targeting specific medical conditions.
Used in Chemical Research:
In the field of chemical research, CBZ-BETA-AMINO-D-ALANINE serves as a valuable compound for studying the properties and reactions of amino acid derivatives. It can be used to explore new reaction pathways and develop innovative synthetic methods.
Used in Material Science:
CBZ-BETA-AMINO-D-ALANINE can be utilized as a building block for the development of novel materials with specific properties, such as enhanced stability or improved biocompatibility. Its application in material science can lead to the creation of advanced materials for various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 62234-37-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,3 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62234-37:
(7*6)+(6*2)+(5*2)+(4*3)+(3*4)+(2*3)+(1*7)=101
101 % 10 = 1
So 62234-37-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N2O4/c12-6-9(10(14)15)13-11(16)17-7-8-4-2-1-3-5-8/h1-5,9H,6-7,12H2,(H,13,16)(H,14,15)/t9-/m1/s1
62234-37-1Relevant articles and documents
Synthesis of (R)- and (S)-2,3-diaminopropyl sulfate: Mechanism based inhibition of glutamate 1-semialdehyde aminomutase
Khayer, Khurshida,Jenn, Thierry,Akhtar, Mahmoud,John, Robert,Gani, David
, p. 1637 - 1641 (2007/10/03)
A short synthesis of each enantiomer of 2,3-diaminopropyl hydrogensulfate is described starting from (2R)- and (2S)-asparagine. The compounds serve as inhibitors for pyridoxal 5'-phosphate-dependent (2S)- glutamate 1-semialdehyde aminotransferase, a target for selective herbicides and antibacterial agents on the tetrapyrrole biosynthetic pathway. The (2R)- enantiomer, as predicted, serves as a potent irreversible inactivator. (C) 2000 Elsevier Science Ltd.
Substituted urido amino and imino acids and esters
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, (2008/06/13)
Compounds of the formula STR1 wherein X is various imino or amino acids or esters are disclosed. These compounds possess angiotensin converting enzyme inhibition activity and depending upon the definition of X also possess enkephalinase inhibition activit
Conversion of serine to stereochemically pure β-substituted α-amino acids via β-lactones
Arnold,Kalantar,Vederas
, p. 7105 - 7109 (2007/10/02)
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