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β-Methylidenphenylalanin, also known as β-methyl-DL-phenylalanine, is a synthetic amino acid derivative characterized by the presence of a methylidene group (-CH2) adjacent to the phenyl ring. β-Methylidenphenylalanin is structurally similar to phenylalanine, a naturally occurring amino acid, but with an additional methyl group and a double bond between the carbons adjacent to the phenyl ring. β-Methylidenphenylalanin has potential applications in the pharmaceutical and chemical industries, particularly in the synthesis of various drugs and other bioactive compounds. Its unique structure allows for the exploration of its properties and potential interactions with biological systems, although further research is needed to fully understand its implications and applications.

71028-59-6

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71028-59-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71028-59-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,2 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 71028-59:
(7*7)+(6*1)+(5*0)+(4*2)+(3*8)+(2*5)+(1*9)=106
106 % 10 = 6
So 71028-59-6 is a valid CAS Registry Number.

71028-59-6Downstream Products

71028-59-6Relevant academic research and scientific papers

Polyenolates of unsaturated carboxylic acids in synthesis. Synthesis of unsaturated α-amino acids and γ-hydrazino acids

Aurell,Gil,Martinez,Parra,Tortajada,Mestres

, p. 1833 - 1839 (2007/10/02)

Regioselective reaction of lithium diene- and triene-diolates 1 and 2 with o-diphenylphosphinyl hydroxylamine affords unsaturated α-amino acids 3 and 4. Addition to DEAD leads selectively to γ-hydrazino unsaturated acids 5 and 6.

Ueber einen neuartigen synthetischen Zugang zu β,γ-ungesaettigten α-Aminocarbonsaeuren

Heinzer, Franz,Bellus, Daniel

, p. 2279 - 2297 (2007/10/02)

A versatile new synthetic pathway for the preparation of β,γ-unsaturated α-amino acids (1) is presented.Cu(I)-catalyzed addition of ethyl isocyanoacetate (2) to α-chloro carbonyl compounds (3) gives 5-chloroalkyl-2-oxazolin-4-carboxylates (4) in high yiel

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