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N-Benzyloxycarbonyl-D-proline

Base Information Edit
  • Chemical Name:N-Benzyloxycarbonyl-D-proline
  • CAS No.:6404-31-5
  • Molecular Formula:C13H15NO4
  • Molecular Weight:249.266
  • Hs Code.:29339900
  • European Community (EC) Number:229-021-5
  • DSSTox Substance ID:DTXSID60214085
  • Nikkaji Number:J207.010C
  • Wikidata:Q69756929
  • Mol file:6404-31-5.mol
N-Benzyloxycarbonyl-D-proline

Synonyms:6404-31-5;Z-D-Pro-OH;N-Benzyloxycarbonyl-D-proline;(+)-Z-D-proline;Z-D-PROLINE;(R)-N-BENZYLOXYCARBONYLPROLINE;N-Carbobenzoxy-D-proline;N-Cbz-D-proline;(2R)-1-phenylmethoxycarbonylpyrrolidine-2-carboxylic acid;MFCD00063228;benzyloxycarbonyl-D-proline;(2R)-1-[(benzyloxy)carbonyl]pyrrolidine-2-carboxylic acid;((Benzyloxy)carbonyl)-D-proline;(R)-1-((Benzyloxy)carbonyl)pyrrolidine-2-carboxylic acid;EINECS 229-021-5;1-Benzyl hydrogen (R)-pyrrolidine-1,2-dicarboxylate;(R)-1-(BENZYLOXYCARBONYL)PYRROLIDINE-2-CARBOXYLIC ACID;1-[(benzyloxy)carbonyl]-d-proline;CBZ-D-PROLINE;N-benzyloxycarbonyI-D-proline;SCHEMBL475715;(+)-Z-D-proline, 98%;(2R)-N-benzyloxycarbonylproline;1-(benzyloxycarbonyl)-d-proline;N-(Benzyloxycarbonyl)-D-proline;DTXSID60214085;CS-M0865;(+)-CARBOBENZYLOXY-D-PROLINE;AKOS015924248;CCG-247547;(+)-N-CARBOBENZYLOXY-D-PROLINE;AC-24082;AS-12748;SY020327;AM20050504;C1730;EN300-121303;M03041;(2R)-1-benzyloxycarbonylpyrrolidine-2-carboxylate;A834624;J-300225;Q-101839;(R)-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester

Suppliers and Price of N-Benzyloxycarbonyl-D-proline
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • N-Benzyloxycarbonyl-D-proline
  • 25g
  • $ 388.00
  • TRC
  • N-(Benzyloxycarbonyl)-D-proline
  • 10g
  • $ 165.00
  • TCI Chemical
  • N-Carbobenzoxy-D-proline >98.0%(HPLC)(T)
  • 25g
  • $ 159.00
  • TCI Chemical
  • N-Carbobenzoxy-D-proline >98.0%(HPLC)(T)
  • 5g
  • $ 54.00
  • Sigma-Aldrich
  • (+)-Z-D-proline 98%
  • 500mg
  • $ 52.90
  • Matrix Scientific
  • Z-D-Pro-OH 95+%
  • 100g
  • $ 360.00
  • Matrix Scientific
  • Z-D-Pro-OH 95+%
  • 10g
  • $ 70.00
  • Iris Biotech GmbH
  • Z-D-Pro-OH
  • 5 g
  • $ 87.75
  • Iris Biotech GmbH
  • Z-D-Pro-OH
  • 25 g
  • $ 236.25
  • Crysdot
  • Z-D-Pro-OH 97%
  • 1000g
  • $ 317.00
Total 159 raw suppliers
Chemical Property of N-Benzyloxycarbonyl-D-proline Edit
Chemical Property:
  • Appearance/Colour:white to off-white crystalline powder 
  • Vapor Pressure:3.06E-08mmHg at 25°C 
  • Melting Point:76-78 °C(lit.) 
  • Refractive Index:40 ° (C=2, EtOH) 
  • Boiling Point:432.3 °C at 760 mmHg 
  • PKA:3.99±0.20(Predicted) 
  • Flash Point:215.3 °C 
  • PSA:66.84000 
  • Density:1.309 g/cm3 
  • LogP:1.81010 
  • Storage Temp.:Store at RT. 
  • Solubility.:Chloroform (Slightly), DMSO (Slightly), Ethanol (Slightly), Methanol (Slightly) 
  • XLogP3:1.7
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:4
  • Exact Mass:249.10010796
  • Heavy Atom Count:18
  • Complexity:312
Purity/Quality:

98%min *data from raw suppliers

N-Benzyloxycarbonyl-D-proline *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Safety Statements: 24/25 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:C1CC(N(C1)C(=O)OCC2=CC=CC=C2)C(=O)O
  • Isomeric SMILES:C1C[C@@H](N(C1)C(=O)OCC2=CC=CC=C2)C(=O)O
  • Uses N-(Benzyloxycarbonyl)-D-proline is an an N-Cbz-protected form of D-proline (P755990). It is used to prepare trichostatin A and trapoxin B analogs as histone deacetylase inhibitors. It is also used to prepare potent and selective nonpeptide inhibitors of caspases 3 and 7.
Technology Process of N-Benzyloxycarbonyl-D-proline

There total 21 articles about N-Benzyloxycarbonyl-D-proline which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With sodium hydroxide; at 0 ℃;
Refernces Edit
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