N-[(Benzyloxy)carbonyl]aspartic acid

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Names

[ CAS No. ]:
4515-21-3

[ Name ]:
N-[(Benzyloxy)carbonyl]aspartic acid

[Synonym ]:
Cbz-DL-aspartic acid
N-Carbobenzoxy-DL-aspartic Acid
N-Cbz-DL-aspartic Acid
Aspartic acid, N-[(phenylmethoxy)carbonyl]-
Carbobenzoxy-L-aspartic acid
N-[(Benzyloxy)carbonyl]aspartic acid
MFCD00063181
CBz-aspartic acid

Chemical & Physical Properties

[ Density]:
1.4±0.1 g/cm3

[ Boiling Point ]:
472.8±45.0 °C at 760 mmHg

[ Melting Point ]:
115ºC

[ Molecular Formula ]:
C12H13NO6

[ Molecular Weight ]:
267.235

[ Flash Point ]:
239.7±28.7 °C

[ Exact Mass ]:
267.074280

[ PSA ]:
116.42000

[ LogP ]:
1.72

[ Vapour Pressure ]:
0.0±1.2 mmHg at 25°C

[ Index of Refraction ]:
1.574

[ Storage condition ]:
Store at RT.

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2924299090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Benzyl chloroformate
  • DL-Aspartic Acid

DownStream

  • (3S)-4-ethoxy-4-oxo-3-(phenylmethoxycarbonylamino)butanoate
  • Z-D-Asp-OH
  • Z-Asp-OH
  • 1-methyl 3-phenyl-N-[N-[(phenylmethoxy)carbonyl]-L-alpha-aspartyl]-L-alaninate
  • Nsc117449
  • z-dehydro-ala-oh

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

Identification of some novel AHAS inhibitors via molecular docking and virtual screening approach.

Bioorg. Med. Chem. 15 , 374-80, (2007)

Acetohydroxyacid synthase (AHAS; EC 2.2.1.6) catalyzes the first common step in branched-chain amino acid biosynthesis. This enzyme is an important target for the design of environmental-benign herbic...


More Articles

Related Compounds

  • N-[(Benzyloxy)carbonyl]-L-aspartic acid 1-(2,4,5-trichlorophenyl)4-benzyl ester
  • N-[(benzyloxy)carbonyl]-L-aspartic acid β-tert-butyl ester α-[3-(trifluoromethyl)benzyl]amide
  • N-[(benzyloxy)carbonyl]-D-aspartic acid β-tert-butyl ester α-[3-(trifluoromethyl)benzyl]amide
  • Z-PHE-ASP-OH
  • Z-Asp-OH
  • Z-D-Asp-OH
  • N-(1-Cyano-1-cyclopropylethyl)-2-[2-pyrrolidin-1-yl-5-(trifluoromethyl)anilino]acetamide
  • 2,3-Dimethyl-6-(piperidin-1-yl)quinoxaline
  • 4-Methyl-2-pyridin-4-yl-1,2,3,4-tetrahydro-isoquinoline
  • 1-(4-Fluorophenyl)-2-iodo-3-(trifluoromethyl)benzene
  • 2-(4-(Methylamino)phenyl)benzo[d]thiazol-5-ol
  • n-(Sec-butyl)-3-(2-ethoxyphenyl)propanamide
  • (2R)-2-(heptafluoropropyl)oxirane
  • (1-Benzyl-1H-indol-5-yl)-quinazolin-4-yl-amine
  • 2-[[[2-(Dimethylamino)phenyl]methyl]amino]ethanol
  • 4-[[(2R,4S)-4-[[(4R,5S,6S)-2-Carboxy-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-en-3-yl]thio]-2-pyrrolidinyl]methyl]-1-(2-hydroxyethyl)-3-methyl-1H-1,2,3-triazolium
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