123098-61-3 Usage
Uses
Used in Pharmaceutical Industry:
BOC-L-2-AMINO-5-METHYLHEX-4-ENOIC ACID is used as a key intermediate in the synthesis of peptides for various pharmaceutical applications. Its presence enhances the reactivity and functionality of the peptides, contributing to the development of new drugs and therapeutic agents.
Used in Materials Science:
In the materials science field, BOC-L-2-AMINO-5-METHYLHEX-4-ENOIC ACID is utilized as a building block for the synthesis of complex organic molecules. Its unique properties allow for the creation of advanced materials with specific characteristics, such as enhanced reactivity or improved stability, which can be applied in various high-tech applications.
Check Digit Verification of cas no
The CAS Registry Mumber 123098-61-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,0,9 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 123098-61:
(8*1)+(7*2)+(6*3)+(5*0)+(4*9)+(3*8)+(2*6)+(1*1)=113
113 % 10 = 3
So 123098-61-3 is a valid CAS Registry Number.
123098-61-3Relevant academic research and scientific papers
Elaridi, Jomana,Jackson, W. Roy,Robinson, Andrea J.
, p. 2025 - 2029 (2005)
The methyl ester derivative of commercially available N-acetyl-allylglycine readily undergoes cross-metathesis with 2-methylbut-2-ene and ruthenium-alkylidene catalyst to afford the prenylglycine derivative. Acid-catalysed cyclisation then affords 5,5-dimethylproline in near quantitative yield and enantioselectivity.
ASYMMETRIC SYNTHESIS OF α-AMINO ACIDS: COMPARISON OF ENOLATE VS. CATION FUNCTIONALIZATION OF N-BOC-5,6-DIPHENYL-2,3,5,6-TETRAHYDRO-4H-1,4-OXAZIN-2-ONES
Williams, Robert M.,Im, Myeong-Nyeo
, p. 6075 - 6078 (2007/10/02)
Enolate generation and subsequent alkylation of the chiral glycinates 1 and 2 occurs with a high degree of diastereoselectivity.Reduction of the homologation products (3 and 4) furnishes with high enantiomeric excess, the N-t-BOC, and free α-amino acid derivates 5 and 6, respectively.
