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

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

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
  • 2-(6-bromo-1H-indol-1-yl)-1-(1,3,4,5-tetrahydro-2H-pyrido[4,3-b]indol-2-yl)ethanone
  • 3,4-dihydro-2H-1,5-benzodioxepin-7-yl(8-methoxy-1,3,4,5-tetrahydro-2H-pyrido[4,3-b]indol-2-yl)methanone
  • N-[1-(2-methoxyethyl)-1H-indol-4-yl]-2-(3-methylbutyl)-1-oxo-1,2-dihydroisoquinoline-4-carboxamide
  • 2-(6-bromo-1H-indol-1-yl)-N-(1-methyl-1H-indol-4-yl)acetamide
  • N-(tetrahydro-2H-pyran-4-ylmethyl)-2-(3,5,9-trimethyl-7-oxo-7H-furo[3,2-g]chromen-6-yl)acetamide
  • N-{[4-(4-methoxyphenyl)tetrahydro-2H-pyran-4-yl]methyl}-1-methyl-1H-indole-2-carboxamide
  • 4-Methylpyrimidine-2-sulfonic acid
  • N-(tetrahydro-2H-pyran-4-ylmethyl)-3-(3,5,9-trimethyl-7-oxo-7H-furo[3,2-g]chromen-6-yl)propanamide
  • 2-(1H-indol-1-yl)-1-(8-methoxy-1,3,4,5-tetrahydro-2H-pyrido[4,3-b]indol-2-yl)ethanone
  • N-(4-(4-(2-amino-2-oxoethyl)-5-oxo-4,5-dihydro-1H-tetrazol-1-yl)phenyl)-2,3-dihydrobenzo[b][1,4]dioxine-2-carboxamide
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