70982-53-5 Usage
Uses
Used in Organic Synthesis:
L-Vinylglycine is used as a precursor for the synthesis of biologically active compounds due to its unique structure and reactivity.
Used in Biochemistry:
L-Vinylglycine is used as a substrate for enzyme-catalyzed reactions, allowing for the study of enzyme mechanisms and the development of new biocatalytic processes.
Used in Agriculture:
L-Vinylglycine is used as a plant growth regulator for its ability to disrupt the biosynthesis of ethylene, a plant hormone involved in the regulation of growth and development. This application can potentially enhance crop yields and improve plant health.
Check Digit Verification of cas no
The CAS Registry Mumber 70982-53-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,9,8 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 70982-53:
(7*7)+(6*0)+(5*9)+(4*8)+(3*2)+(2*5)+(1*3)=145
145 % 10 = 5
So 70982-53-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H7NO2/c1-2-3(5)4(6)7/h2-3H,1,5H2,(H,6,7)/t3-/m0/s1
70982-53-5Relevant academic research and scientific papers
Synthesis of enantiomerically enriched β,γ-unsaturated-α-amino acids
Rose, Nicholas G.W,Blaskovich, Mark A,Wong, Alex,Lajoie, Gilles A
, p. 1497 - 1507 (2007/10/03)
A variety of enantiomerically enriched β,γ-unsaturated-α-amino acids are synthesized by olefination of a Cbz-protected serine aldehyde equivalent, readily prepared from serine. A cyclic ortho ester protecting group is employed to minimize racemization. The deprotected amino acids are obtained in good yield, ranging from 70-95% ee, with double-bond geometry determined by the type of Wittig reagent used. Isotopically labeled side chains are readily introduced by this procedure, and free γ-13C-vinylglycine was prepared in 44% yield from the protected serine aldehyde synthon.
