H-Phe-OEt.HCl

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Names

[ CAS No. ]:
3182-93-2

[ Name ]:
H-Phe-OEt.HCl

[Synonym ]:
Ethyl L-phenylalaninate hydrochloride (1:1)
L-Phenylalanine, ethyl ester, hydrochloride (1:1)
L-Phenylalanine Ethyl Ester Hydrochloride
PHENYLALANINE-OET HCL
D,L-phenylalanine ethyl ester hydrochloride
H-Phe-OEt.HCl
L-Phe-OEt.HCL
Ethyl L-phenylalanin
H-L-Phe-OEt*HCl
L-Phe-OEt hydrochloride
Ethyl L-Phenylalaninate Hydrochloride
L-phenylalanine ethylester
Phe-OEt HCl
L-PHENYLALANINE ETHYL ESTER HCL
EINECS 221-673-9
L-PHANYLALANINEETHYLESTERHCL
MFCD00012507
ethyl L-phenylalanine hydrochloride

Chemical & Physical Properties

[ Boiling Point ]:
281.3ºC at 760mmHg

[ Melting Point ]:
155-156 °C(lit.)

[ Molecular Formula ]:
C11H16ClNO2

[ Molecular Weight ]:
229.703

[ Flash Point ]:
140.3ºC

[ Exact Mass ]:
229.086960

[ PSA ]:
52.32000

[ LogP ]:
2.62180

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S22-S24/25-S26

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29224995

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Ethanol
  • L-Phenylalanine
  • (3S,5R)-2,3,5,6-tetrahydro-5-phenyl-3,4-bis(phenylmethyl)-4H-1,4-oxazin-2-one
  • Benzyl bromide
  • (3R,5R)-3-benzyl-4-tert-butyloxycarbonyl-5-phenyl-2,3,5,6-tetrahydro-4H-1,4-oxazin-2-one

DownStream

  • H-Phe-ol
  • D-phenylalaninol
  • (2S,5S)-(-)-2-tert-Butyl-3-methyl-5-benzyl-4-imidazolidinone
  • 2,5-Piperazinedione,3,6-bis(phenylmethyl)-
  • ethene
  • Carbon dioxide
  • 2-Phenylethanamine
  • (S)-(-)-N-(3-PENTYL)-1-PHENYLETHYLAMINEHYDROCHLORIDE
  • (2S)-2-Amino-1,1,3-triphenyl-1-propanol
  • (S)-Cbz-Phenylalaninol

Customs

[ HS Code ]: 29224995

Articles

Optimisation of a system for the co-translational incorporation of a keto amino acid and its application to a tumour-specific Anticalin.

Protein Eng. Des. Sel. 28 , 553-65, (2015)

The bioorthogonal keto group has attracted interest for the site-specific chemical conjugation of recombinant proteins under mild conditions, e.g. with aminooxy-functionalised fluorescent probes, radi...


More Articles

Related Compounds

  • H-Phe-Met-Arg-Phe-NH2 acetate salt
  • H-Phe-Phe-NH2
  • H-Phe(4-Br)-Ome.HCl
  • H-Phe-Asp-Lys-OH
  • H-PHE-LEU-GLU-GLU-ILE-OH
  • H-Phe-Ser(Bu-t)-OH
  • 1-(2-methyl-5-oxocyclohexyl)-1H-pyrrole-2-carbonitrile
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • 3-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)benzoyl]-2-methyl-1,3-thiazolidine-4-carboxylic acid
  • 1-{[3-cyclopropyl-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)butanamido]methyl}cyclopropane-1-carboxylic acid
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • methyl 2-amino-2-(7-nitro-1H-indol-3-yl)acetate