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1214028-21-3

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1214028-21-3 Usage

General Description

FMOC-BETA-METHYL-DL-PHENYLALANINE is a chemical compound used in the synthesis and study of peptides and proteins. Its molecular structure consists of a beta-methyl group attached to the alpha carbon of a phenylalanine residue, which confers unique properties to the compound. The FMOC (9-fluorenylmethoxycarbonyl) protective group is commonly used in peptide synthesis to protect the amine group of amino acids, allowing for the stepwise assembly of peptide chains. The presence of the FMOC group also facilitates purification of the peptide product. FMOC-BETA-METHYL-DL-PHENYLALANINE is widely utilized in the fields of pharmaceuticals and biochemistry for the creation and analysis of peptides and proteins.

Check Digit Verification of cas no

The CAS Registry Mumber 1214028-21-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,4,0,2 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1214028-21:
(9*1)+(8*2)+(7*1)+(6*4)+(5*0)+(4*2)+(3*8)+(2*2)+(1*1)=93
93 % 10 = 3
So 1214028-21-3 is a valid CAS Registry Number.

1214028-21-3Downstream Products

1214028-21-3Relevant articles and documents

Use of β-Methylphenylalanine (βMeF) Residues To Probe the Nature of the Interaction of Substance P with Its Receptor: Effects of βMeF-Containing Substance P Analogs on Rabbit Iris Smooth Muscle Contraction

Birney, David M.,Cole, Derek C.,Crosson, Craig E.,Kahl, Brenda F.,Neff, Bart W.,et al.

, p. 2478 - 2482 (1995)

The effects of substituting (2S,3S)-β-methylphenylalanine (S-βMeF) or (2S,3R)-β-methylphenylalanine (R-βMeF) for the Phe7 and/or Phe8 residues of the tachykinin substance P (SP, RPKPQQFFGLM-NH2) upon the ability of SP to stimulate co

(2R,1'S,2'R)- And (2S,1'S,2'R)-3-[2-mono(di,tri)fluoromethylcyclopropyl] alanines and their incorporation into hormaomycin analogues

De Meijere, Armin,Kozhushkov, Sergei I.,Yufit, Dmitrii S.,Grosse, Christian,Kaiser, Marcel,Raev, Vitaly A.

, p. 2844 - 2857 (2015/02/19)

Efficient and scalable syntheses of enantiomerically pure (2 R ,1' S ,2' R )- and (2 S ,1' S ,2' R )-3-[2-mono(di,tri)fluoromethylcyclopropyl] alanines 9a - c , as well as allo-D-threonine ( 4 ) and ( 2 S,3R)-β-methylphenylalanine (3), using the Belokon' approach with (S )- and (R )-2-[( N-benzylprolyl)amino]benzophenone [(S)- and (R)-10 ] as reusable chiral auxiliaries have been developed. Three new fluoromethyl analogues of the naturally occurring octadepsipeptide hormaomycin ( 1 ) with (fluoromethylcyclopropyl) alanine moieties have been synthesized and subjected to preliminary tests of their antibiotic activity.

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