CAS 13734-34-4|Boc-L-phenylalanine

Introduction：Basic information about CAS 13734-34-4|Boc-L-phenylalanine, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Table of Contents

1. Names
2. Boc-L-phenylalanine BiologicalActivity
3. Chemical & Physical Properties
4. Safety Information
5. Customs
6. Articles10
7. Synonyms

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

Names

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

Boc-L-phenylalanine BiologicalActivity

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	Research Areas >>OthersSignaling Pathways >>Others >>Others

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

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

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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