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Boc-L-phenylalanine

Names

[ CAS No. ]:
13734-34-4

[ Name ]:
Boc-L-phenylalanine

[Synonym ]:
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

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]:

Research Areas >> Others
Signaling 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

[ Storage condition ]:
-20°C

MSDS

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

Precursor & DownStream

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%

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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...


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Related Compounds

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