1932326-29-8 Usage
Description
(R)-2-(3'-butenyl) alanine is a non-proteinogenic alpha-amino acid derivative of alanine, featuring an additional butenyl group attached to the alpha carbon. This chiral compound is not commonly found in proteins and serves as a valuable building block in organic synthesis and chemical research, particularly in the synthesis of complex molecules and pharmaceuticals. Its unique structure and reactivity contribute to its utility in various applications within the field of organic chemistry.
Uses
Used in Organic Synthesis:
(R)-2-(3'-butenyl) alanine is used as a building block for the synthesis of complex organic molecules, leveraging its unique structure and reactivity to facilitate the creation of novel compounds with potential applications in various industries.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (R)-2-(3'-butenyl) alanine is utilized as a key component in the development of new drugs, contributing to the design and synthesis of innovative medicinal compounds with potential therapeutic benefits.
Used in Chemical Research:
(R)-2-(3'-butenyl) alanine serves as a valuable tool in chemical research, enabling scientists to explore its properties and reactivity, furthering the understanding of organic chemistry and its applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1932326-29-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,9,3,2,3,2 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1932326-29:
(9*1)+(8*9)+(7*3)+(6*2)+(5*3)+(4*2)+(3*6)+(2*2)+(1*9)=168
168 % 10 = 8
So 1932326-29-8 is a valid CAS Registry Number.
1932326-29-8Relevant articles and documents
Influence of α-methylation in constructing stapled peptides with olefin metathesis
Zhang, Qingzhou,Shi, Xiaodong,Jiang, Yanhong,Li, Zigang
, p. 7621 - 7626 (2014/12/11)
Ring-closing metathesis is commonly utilized in peptide macro-cyclization. The influence of α-methylation of the amino acids bearing the olefin moieties has never been systematically studied. In this report, controlled reactions unambiguously indicate that α-methylation at the N-terminus of the metathesis sites is crucial for this reaction to occur. Also, we first elucidated that the E-isomers of stapled peptides are significantly more helical than the Z-isomers.
