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L-3-Cyanophenylalanine

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L-3-Cyanophenylalanine manufacturers

  • L-3-Cyanophenylalanine
  • L-3-Cyanophenylalanine pictures
  • $1.00
  • 2019-08-02
  • CAS:57213-48-6
  • Min. Order: 1KG
  • Purity: 95-99%
  • Supply Ability: 500kg/month
L-3-Cyanophenylalanine Basic information
Product Name:L-3-Cyanophenylalanine
Synonyms:(2S)-2-ammonio-3-(3-cyanophenyl)propanoate;(S)-N-3-Cyanophenylalanine(e.e.);(2R)-2-amino-3-(3-cyanophenyl)propanoic acid;(M-CN)PHE-OH;M-CYANO-L-PHENYLALANINE;L-3-CYANOPHENYLALANINE;L-3-CYANOPHE;H-M-CYANO-L-PHE-OH
CAS:57213-48-6
MF:C10H10N2O2
MW:190.2
EINECS:
Product Categories:Phenylalanine analogs and other aromatic alpha amino acids;a-amino;Amino Acids
Mol File:57213-48-6.mol
L-3-Cyanophenylalanine Structure
L-3-Cyanophenylalanine Chemical Properties
Melting point 235-239 °C
Boiling point 325.7°C (rough estimate)
density 1.2167 (rough estimate)
refractive index 1.6300 (estimate)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form Powder
pka2.14±0.10(Predicted)
color White to slightly yellow
InChIInChI=1S/C10H10N2O2/c11-6-8-3-1-2-7(4-8)5-9(12)10(13)14/h1-4,9H,5,12H2,(H,13,14)/t9-/m0/s1
InChIKeyZHUOMTMPTNZOJE-VIFPVBQESA-N
SMILESC(O)(=O)[C@H](CC1=CC=CC(C#N)=C1)N
CAS DataBase Reference57213-48-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xn
Risk Statements 20/21/22
Safety Statements 26-37/39-37/38
RIDADR UN3439
HazardClass 6.1
PackingGroup III
HS Code 29225090
MSDS Information
ProviderLanguage
ACROS English
L-3-Cyanophenylalanine Usage And Synthesis
Chemical Propertieswhite to slightly yellow powder
UsesH-Phe(3-CN)-OH is a phenylalanine derivative[1].
Antimicrobial activityL-3-Cyanophenylalanine (3CP) is a β-amino acid that has been shown to have an interaction with serine protease. 3CP is an antibacterial agent that is used in the treatment of bacterial infections. It has been shown to inhibit the growth of bacteria by inhibiting the acid transporter, which leads to a decrease in intracellular pH. 3CP binds to the basic group of the enzyme and forms a covalent bond, inhibiting its function. The synthesis of 3CP can be achieved through synthetic chemistry or by enzymatic conversion from L-serine. This compound can also be obtained as an enantiomer, meaning it has two different forms: one that is active and one that is inactive.
References[1] Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-828. DOI:10.1080/10408398.2012.708368
L-3-Cyanophenylalanine Preparation Products And Raw materials
Preparation ProductsFMOC-L-3-CYANOPHENYLALANINE
Tag:L-3-Cyanophenylalanine(57213-48-6) Related Product Information
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