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Z-TRP-ONP

Product Name
Z-TRP-ONP
CAS No.
16624-64-9
Chemical Name
Z-TRP-ONP
Synonyms
Z-TRP-ONP;Z-L-Trp-ONp;CBZ-Trp-Onp;Z-TRYPTOPHAN-ONP;Einecs 240-674-5;Z-L-TRYPTOPHAN P-NITROPHENYL ESTER;Z-L-TRYPTOPHAN 4-NITROPHENYL ESTER;Nα-Z-L-tryptophan 4-nitrophenyl ester;N-CBZ-L-TRYPTOPHAN P-NITROPHENYL ESTER;Nα-Z-L-tryptophan 4-nitrophenyl ester99%
CBNumber
CB8745930
Molecular Formula
C25H21N3O6
Formula Weight
459.45
MOL File
16624-64-9.mol
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Z-TRP-ONP Property

Melting point:
102-104 °C
storage temp. 
Sealed in dry,2-8°C
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Safety

WGK Germany 
3
F 
3-10-21
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
B700168
Product name
N-(Benzyloxycarbonyl)-L-tryptophanp-NitrophenylEster
Packaging
25g
Price
$120
Updated
2021/12/16
TRC
Product number
B700168
Product name
N-(Benzyloxycarbonyl)-L-tryptophanp-NitrophenylEster
Packaging
100g
Price
$415
Updated
2021/12/16
Chem-Impex
Product number
02263
Product name
Nα-Z-L-tryptophan4-nitrophenylester,≥97%(HPLC)
Purity
≥97%(HPLC)
Packaging
100G
Price
$506.69
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
AAA0003902
Product name
Z-TRP-ONP
Purity
95.00%
Packaging
1G
Price
$617
Updated
2021/12/16
AK Scientific
Product number
8455AA
Product name
(S)-4-Nitrophenyl2-(((benzyloxy)carbonyl)amino)-3-(1H-indol-3-yl)propanoate
Packaging
100g
Price
$637
Updated
2021/12/16
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Z-TRP-ONP Chemical Properties,Usage,Production

Uses

N-(Benzyloxycarbonyl)-L-tryptophan p-Nitrophenyl Ester is used in the synthesis of tryptophan containing dipeptides as potent PPARy antagonists.. N-(Benzyloxycarbonyl)-L-tryptophan p-Nitrophenyl Ester has also been shown to self-assemble on the surface of monolayer protected gold nanoparticles to form a catalytic system for transesterification reactions.

Z-TRP-ONP Preparation Products And Raw materials

Raw materials

Preparation Products

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Z-TRP-ONP Suppliers

China 30 Germany 2 India 1 Japan 1 Switzerland 2 United States 13 Global 49
IRIS Biotech GmbH
Tel
--
Fax
--
Country
Germany
ProdList
4426
Advantage
68
Service Chemical Inc.
Tel
--
Fax
--
Email
sales@chemos-group.com
Country
Germany
ProdList
6350
Advantage
71

16624-64-9, Z-TRP-ONPRelated Search:

N-Cbz-L-Tryptophan Z-Trp-OEt Z-Trp-Lys(Boc)-NH2 Z-TRP-NH2 Z-TRP-OME Z-TRP-TRP-OH Z-PHE-ALA-OH Z-TRP(BOC)-OH DCHA Z-TRP-OSU Z-TRP-OBZL Z-VAL-TRP-OH Z-SER-NHNH2 Z-PHE-TRP-OH tert-butyl N-[(5S)-6-amino-5-[[(2S)-3-(1H-indol-3-yl)-2-(phenylmethoxycarbonylamino)propanoyl]amino]-6-oxohexyl]carbamate Z-ASP-OME N-Cbz-L-Aspartic acid 4-benzyl ester Z-TLE-OH DCHA Z-L-METHIONINE METHYL ESTER

  • BENZYLOXYCARBONYL-L-TRYPTOPHAN P-NITROPHENYL ESTER
  • N-ALPHA-BENZYLOXYCARBONYL-L-TRYPTOPHAN-4-NITROPHENYL ESTER
  • N-BENZYLOXYCARBONYL-L-TRYPTOPHAN-4-NITROPHENYL ESTER
  • N-CBZ-L-TRYPTOPHAN P-NITROPHENYL ESTER
  • N-CARBOBENZOXY-L-TRYPTOPHAN-P-NITROPHENYL ESTER
  • Z-L-TRYPTOPHAN 4-NITROPHENYL ESTER
  • Z-L-TRYPTOPHAN P-NITROPHENYL ESTER
  • Z-TRP-ONP
  • Z-TRYPTOPHAN-ONP
  • N-CBZ-L-Tryptophan p-nitrophenyl ester N-Carbobenzyloxy-L-tryptophan p-nitrophenyl ester
  • 4-nitrophenyl N-(benzyloxycarbonyl)-L-tryptophanate
  • N-Carbobenzoxy-L-tryptophan-p-nitrophenyester
  • N-alpha-Benzyloxycarbonyl-L-tryptophane p-nitrophenyl ester
  • Z-L-Trp-ONp
  • Nalpha-carbobenzyloxy-L-tryptophan p-nitrophenyl ester
  • Einecs 240-674-5
  • (S)-4-Nitrophenyl 2-(((benzyloxy)carbonyl)aMino)-3-(1H-indol-3-yl)propanoate
  • 4-Nitrophenyl N-[(benzyloxy)carbonyl]tryptophanate
  • (2S)-2-(benzyloxycarbonylamino)-3-(1H-indol-3-yl)propionic acid (4-nitrophenyl) ester
  • (2S)-3-(1H-indol-3-yl)-2-[[oxo-(phenylmethoxy)methyl]amino]propanoic acid (4-nitrophenyl) ester
  • (4-nitrophenyl) (2S)-3-(1H-indol-3-yl)-2-(phenylmethoxycarbonylamino)propanoate
  • Nα-Z-L-tryptophan 4-nitrophenyl ester99%
  • 4-nitrophenyl (2S)-2-{[(benzyloxy)carbonyl]amino}-3-(1H-indol-3-yl)propanoate
  • L-Tryptophan, N-[(phenylmethoxy)carbonyl]-, 4-nitrophenyl ester
  • Nα-Z-L-tryptophan 4-nitrophenyl ester
  • CBZ-Trp-Onp
  • 4-Nitrophenyl ((benzyloxy)carbonyl)-L-tryptophanate
  • 16624-64-9
  • C25H21N3O6
  • Peptide Synthesis
  • Specialty Synthesis
  • Tryptophan
  • Amino Acid Derivatives