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BOC-D-4-Fluorophe

BOC-D-4-Fluorophe Structure
BOC-D-4-Fluorophe structure
CAS No.
57292-45-2
Chemical Name:
BOC-D-4-Fluorophe
Synonyms
Boc-D-4-F-Phe;BOC-D-4-FLUOROPHE;BOC-D-PHE(4-F)-OH;BOC-D-PHE(P-F)-OH;BOC-4-FLUORO-D-PHE;RARECHEM BK PT 0035;BOC-P-FLUORO-D-PHE-OH;BOC-4-FLUORO-D-PHE-OH;Boc-D-4-Fluoro-phe-OH;Boc-D-Phe(4-F)-OH,98%
CBNumber:
CB2389932
Molecular Formula:
C14H18FNO4
Molecular Weight:
283.3
MDL Number:
MFCD00079669
MOL File:
57292-45-2.mol
Last updated:2023-04-23 13:52:06

BOC-D-4-Fluorophe Properties

Melting point 83-86 °C
alpha -8 º (c=1,MeOH)
Boiling point 431.2±40.0 °C(Predicted)
Density 1.1918 (estimate)
storage temp. Sealed in dry,2-8°C
solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form powder to crystal
pka 3.87±0.10(Predicted)
color White to Almost white
CAS DataBase Reference 57292-45-2(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302+H312+H332-H315-H319-H227
Precautionary statements  P501-P261-P270-P210-P271-P264-P280-P370+P378-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330-P302+P352+P312-P304+P340+P312-P403+P235
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  37/39-26-24/25
WGK Germany  3
Hazard Note  Irritant/Keep Cold
HS Code  29242990

BOC-D-4-Fluorophe Chemical Properties,Uses,Production

Chemical Properties

white to light yellow crystal powde

Uses

Boc-D-4-Fluorophenylalanine, is an amino acid building block used in peptide synthesis. With a growing peptide drug market the fast, reliable synthesis of peptides is of great importance.

BOC-D-4-Fluorophe Preparation Products And Raw materials

Raw materials

Preparation Products

57292-45-2(BOC-D-4-Fluorophe )Related Search:

D-Phenylalanine D-Alanine DL-Phenylalanine L-Phenylalanine N-(tert-Butoxycarbonyl)-L-phenylalanine
tert-Butanol N-Carbobenzyloxyglycine Phenprobamate Boc-Aib-OH EC 2.6.1.2
BOC-GLY-LEU-OH Fluorine BOC-D-4-Fluorophe BOC-D-3,4-Difluorophe BOC-L-3-FLUOROPHE
BOC-D-2-FLUOROPHE BOC-D-3-FLUOROPHE BOC-L-2-FLUOROPHE

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BOC-D-4-FLUOROPHE BOC-(R)-2-AMINO-3-(4'-FLUOROPHENYL)PROPANOIC ACID BOC-P-FLUORO-D-PHENYLALANINE BOC-P-FLUORO-D-PHE-OH BOC-4-FLUORO-D-PHE BOC-4-FLUORO-D-PHENYLALANINE BOC-4-FLUORO-D-PHE-OH BOC-D-PHE(P-F)-OH BOC-D-PHE(4-F)-OH (R)-N-BOC-4-FLUOROPHENYLALANINE RARECHEM BK PT 0035 tert-butoxycarbonyl-d-4-fluorophenylalanine N-ALPHA-TERT-BUTYLOXYCARBONYL-D-4-FLUOROPHENYLALANINE N-ALPHA-T-BOC-4-FLUORO-D-PHENYLALANINE N-T-BUTOXYCARBONYL-P-FLUORO-D-PHENYLALANINE N-TERT-BUTOXYCARBONYL-4-FLUOROPHENYL-D-ALANINE (R)-2-TERT-BUTOXYCARBONYLAMINO-3-(4-FLUORO-PHENYL)-PROPIONIC ACID BOC-D-4-FLUOROPHENYLALANINE D-4-FLUOROPHENYLALANINE, BOC PROTECTED 2-tert-Butoxycarbonylamino-3-(4-fluoro-phenyl)-propionic acid N-T-BOC-P-FLUORO-D-PHENYLALANINE N-alpha-tert-Butoxycarbonyl-3-(4-fluorophenyl)-D-al BOC-D-4-FLUOROPHENYLALANINE 98% N-tert-Butoxy-D-4-Fluoro Phenylalanine 4-Fluoro-D-phenylalanine,N-BOCprotected N-alpha-t-Butyloxycarbonyl-4-fluoro-D-phenylalanine (R)-Boc-2-amino-3-(4-fluorophenyl)propionic acid Boc-4-fluoro-D-phenylalanine99% Boc-D-Phe(4-F) -OH Boc-4-Fluoro-D-Phenylalanine N-Boc-4-fluoro-D-phenylalanine Boc-D-Phe(4-F)-OH Boc-4-fluoro-D-phenylalanine Boc-p-fluoro-D-Phe-OH N-ALPHA-T-BUTYLOXYCARBONYL-D-4-FLUOROPHENYLALANINE N-(tert-butoxycarbonyl)-p-fluoro-D-phenylalanine (R)-N-BOC-4-FLUOROPHENYLALANINE, 95%, 98% EE (R)-N-BOC-4-Fluorophenylalanine, 98% ee Boc-D-4-Fluoro-phe-OH N-(tert-Butoxycarbonyl)-4-fluoro-D-phenylalanine (R)-2-((tert-Butoxycarbonyl)aMino)-3-(4-fluorophenyl)propanoic acid N-Boc-4-fluoro-D-phenylalanine, 95% (Tert-Butoxy)Carbonyl D-Phe(4-F)-OH 4-Fluoro-D-phenylalanine, N-BOC protected 95+% N-[(1,1-Dimethylethoxy)carbonyl]-4-fluoro-D-phenylalanine Boc-D-4-F-Phe (2R)-3-(4-fluorophenyl)-2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]propanoate N-(tert-Butoxycarbonyl)-4-fluoro-D-phenylalanine > D-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-4-fluoro- Boc-D-Phe(4-F)-OH,98% Venadaparib Impurity 71 57292-45-2 C14H17FNO4 Phenylalanine Derivatives Peptide Synthesis Specialty Synthesis Unnatural Amino Acid Derivatives Phenylalanine analogs and other aromatic alpha amino acids Phenylalanine [Phe, F] Unusual Amino Acids Boc-Amino acid series