Boc-L-phenylalanine

Modify Date: 2025-08-23 16:35:31

Boc-L-phenylalanine Structure
Boc-L-phenylalanine structure
 Common Name Boc-L-phenylalanine
CAS Number 13734-34-4 Molecular Weight 265.31
Density 1.2±0.1 g/cm3 Boiling Point 426.6±38.0 °C at 760 mmHg
Molecular Formula C14H19NO4 Melting Point 85-87 °C(lit.)
MSDS USA Flash Point 211.8±26.8 °C

 Use of Boc-L-phenylalanine


Boc-L-phenylalanine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

 Names

Name N-(tert-Butoxycarbonyl)-L-phenylalanine
Synonym More Synonyms

 Boc-L-phenylalanine Biological Activity

Description Boc-L-phenylalanine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 426.6±38.0 °C at 760 mmHg
Melting Point 85-87 °C(lit.)
Molecular Formula C14H19NO4
Molecular Weight 265.31
Flash Point 211.8±26.8 °C
Exact Mass 265.131409
PSA 75.63000
LogP 2.96
Vapour Pressure 0.0±1.1 mmHg at 25°C
Index of Refraction 1.528
InChIKey ZYJPUMXJBDHSIF-UHFFFAOYSA-N
SMILES CC(C)(C)OC(=O)NC(Cc1ccccc1)C(=O)O
Storage condition -20°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xn,Xi
Risk Phrases R36
Safety Phrases S39-S26
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2924299090

 Synthetic Route

 Customs

HS Code 2924299090
Summary 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Articles10

More Articles
Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Nat. Chem. Biol. 5 , 45-52, (2009)

Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting tr...

Investigation of dendriplexes by ion mobility-mass spectrometry.

Molecules 19(12) , 20731-50, (2014)

Highly branched polyamidoamine (PAMAM) dendrimers presenting biological activities have been envisaged as non-viral gene delivery vectors. They are known to associate with nucleic acid (DNA) in non-co...

NMR spectroscopic detection of chirality and enantiopurity in referenced systems without formation of diastereomers.

Nat. Commun. 4 , 2188, (2013)

Enantiomeric excess of chiral compounds is a key parameter that determines their activity or therapeutic action. The current paradigm for rapid measurement of enantiomeric excess using NMR is based on...

 Synonyms

N-tert-Butyloxycarbonyl-L-phenylalanine
Boc-phenylalanine
EINECS 237-305-5
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-phenylalanine
Boc-L-Phenylalanine
(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoic acid
(2S)-2-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-3-phenylpropanoic acid
N-(tert-Butoxycarbonyl)-L-phenylalanin
(S)-2-((tert-Butoxycarbonyl)amino)-3-phenylpropanoic acid
N-(tert-Butoxycarbonyl)-L-phenylalanine
boc-L-Phe
L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-
N-t-Butyloxycarbonyl-L-phenylalanine
L-Phenylalanine, N-((1,1-dimethylethoxy)carbonyl)-
N-α-t-BOC-L-phenylalanine
N-Boc-L-phenylalanine
MFCD00002663
Boc-Phe-OH
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