Boc-L-aspartic acid 4-benzyl ester
Suppliers
Names
[ CAS No. ]:
7536-58-5
[ Name ]:
Boc-L-aspartic acid 4-benzyl ester
[Synonym ]:
(2S)-4-(benzyloxy)-2-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid (non-preferred name)
EINECS 231-406-8
N-tert-Butoxycarbonyl-L-aspartic acid 4-benzyl ester
MFCD00065564
(2S)-4-(Benzyloxy)-2-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-4-oxobutanoic acid
(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxo-4-phenylmethoxybutanoic acid
L-Aspartic acid, N-((1,1-dimethylethoxy)carbonyl)-, 4-(phenylmethyl) ester
L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 4-(phenylmethyl) ester
N-α-t-BOC-L-aspartic-β-benzyl ester
Boc-Asp(OBzl)-OH
Boc-L-asparticacid4-benzylester
Chemical & Physical Properties
[ Density]:
1.2±0.1 g/cm3
[ Boiling Point ]:
508.1±50.0 °C at 760 mmHg
[ Melting Point ]:
98-102ºC
[ Molecular Formula ]:
C16H21NO6
[ Molecular Weight ]:
323.341
[ Flash Point ]:
261.1±30.1 °C
[ Exact Mass ]:
323.136902
[ PSA ]:
101.93000
[ LogP ]:
3.24
[ Vapour Pressure ]:
0.0±1.4 mmHg at 25°C
[ Index of Refraction ]:
1.527
MSDS
Safety Information
[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
[ Hazard Codes ]:
Xn
[ Safety Phrases ]:
S22-S24/25
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2924299090
Synthetic Route
Precursor & DownStream
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%
Articles
Biochem. Biophys. Res. Commun. 107(1) , 246-9, (1982)
J. Biol. Chem. 259(7) , 4272-8, (1984)
The rat liver microsomal vitamin K-dependent carboxylase has been shown to carboxylate the aspartyl residue in N alpha-t-butyloxycarbonylaspartic acid alpha-benzyl ester to a beta-carboxyaspartyl resi...
Dalton Trans. (1) , 154-62, (2007)
The amino acid derivative Boc-Asp-OBzl (Boc=N-butyloxycarbonyl; Asp=aspartic acid; Bzl=benzyl) was functionalized by coupling its carboxylate side chain to dipicolylamine. This yielded the tridentate ...