Benzyl 5-amino-4-[(tert-butoxycarbonyl)amino]-5-oxopentanoate

Base Information

• Chemical Name: Benzyl 5-amino-4-[(tert-butoxycarbonyl)amino]-5-oxopentanoate
• CAS No.: 292870-04-3
• Molecular Formula: C₁₇H₂₄N₂O₅
• Molecular Weight: 336.388
• Hs Code.: 2921490090
• UNII: C27S4SRN7U
• Mol file: 292870-04-3.mol

Synonyms:292870-04-3;C27S4SRN7U;UNII-C27S4SRN7U;benzyl 5-amino-4-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxopentanoate;BENZYL 5-AMINO-4-[(TERT-BUTOXYCARBONYL)AMINO]-5-OXOPENTANOATE;tert-Butyloxycarbonyl-DL-isoglutamine benzyl ester;Pentanoic acid, 5-amino-4-(((1,1-dimethylethoxy)carbonyl)amino)-5-oxo-, phenylmethyl ester;SCHEMBL10887447;STK366970;AKOS005444220;benzyl N~2~-(tert-butoxycarbonyl)-alpha-glutaminate;benzyl 4-{[(tert-butoxy)carbonyl]amino}-4-carbamoylbutanoate

Chemical Property of Benzyl 5-amino-4-[(tert-butoxycarbonyl)amino]-5-oxopentanoate

Chemical Property:

• Vapor Pressure: 1.03E-11mmHg at 25°C
• Refractive Index: 1.524
• Boiling Point: 539.6 °C at 760 mmHg
• PKA: 11.14±0.46(Predicted)
• Flash Point: 280.2 °C
• PSA: 107.72000
• Density: 1.168 g/cm³
• LogP: 2.97980
• XLogP3: 1.6
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 10
• Exact Mass: 336.16852187
• Heavy Atom Count: 24
• Complexity: 439

Purity/Quality:

98.5% ^*data from raw suppliers

(S)-BENZYL 4-AMINO-5-(AMINOCARBONYL)PENTANOATE, N4-BOC PROTECTED 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)(C)OC(=O)NC(CCC(=O)OCC1=CC=CC=C1)C(=O)N

Technology Process of Benzyl 5-amino-4-[(tert-butoxycarbonyl)amino]-5-oxopentanoate

There total 1 articles about Benzyl 5-amino-4-[(tert-butoxycarbonyl)amino]-5-oxopentanoate 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:

Reference yield:

→ 4-tert-Butoxycarbonylamino-4-carbamoyl-butyric acid benzyl ester (292870-04-3)

Guidance literature:

entspr. Saeurechlorid, NH3;