70982-53-5 Usage
General Description
L-Vinylglycine, also known as 2-amino-4-vinylbutanoic acid, is a chemical compound that is commonly used in the field of organic synthesis and biochemistry. It is a derivative of glycine and contains a vinyl group (-CH=CH2) at the fourth carbon position. L-Vinylglycine is a versatile molecule with various potential applications, including as a precursor for the synthesis of biologically active compounds and as a substrate for enzyme-catalyzed reactions. It has also been studied for its potential use in agriculture as a plant growth regulator due to its ability to disrupt the biosynthesis of ethylene, a plant hormone involved in the regulation of growth and development. Overall, L-Vinylglycine is a valuable chemical compound with diverse applications in research and industry.
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 articles and documents
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.
