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 alanine and proline amino acids with amino or guanidinium substitution on the side chain
Zhang, Zhenyu,Aerschot, Arthur Van,Hendrix, Chris,Busson, Roger,David, Frank,Sandra, Pat,Herdewijn, Piet
, p. 2513 - 2522 (2007/10/03)
Competitive binding of peptides containing basic amino acids to disrupt or prevent the Tat-TAR interaction could result in diminished transcription as well as translation and hence constitutes an alternative way of controlling HIV replication. Therefore, we synthesized guanidinium and amino containing amino acids, based on a proline or an alanine scaffold. The introduction of the guanidinium moiety was best accomplished using 1H- pyrazole-1-carboxamidine hydrochloride, with Pmc used for its protection. The absence of racemization, maintained throughout the whole synthesis, was confirmed by chiral purity determination. These building blocks were smoothly incorporated into oligopeptides, which proved their suitability for use in a combinatorial approach for selecting TAR binding ligands. (C) 2000 Elsevier Science Ltd.
Synthesis and NMDA antagonistic properties of the enantiomers of 4-(3-phosphonopropyl)piperazine-2-carboxylic acid (CPP) and of the unsaturated analogue (E)-4-(3-phosphonoprop-2-enyl)piperazine-2-carboxylic acid (CPP-ene)
Aebischer,Frey,Haerter,Herrling,Mueller,Olverman,Watkins
, p. 1043 - 1051 (2007/10/02)
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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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