Z-L-proline beta-naphthylamide

Base Information

Chemical Name:Z-L-proline beta-naphthylamide
CAS No.:86925-99-7
Molecular Formula:C₂₃H₂₂N₂O₃
Molecular Weight:374.439
Hs Code.:
European Community (EC) Number:635-928-0
DSSTox Substance ID:DTXSID90435802
Wikidata:Q76415141
Mol file:86925-99-7.mol

Synonyms:Z-L-proline beta-naphthylamide;86925-99-7;(S)-Benzyl 2-(naphthalen-2-ylcarbamoyl)pyrrolidine-1-carboxylate;benzyl (2S)-2-(naphthalen-2-ylcarbamoyl)pyrrolidine-1-carboxylate;Z-Pro-NA;SCHEMBL4613461;DTXSID90435802;(S)-Benzyl2-(naphthalen-2-ylcarbamoyl)pyrrolidine-1-carboxylate

Suppliers and Price of Z-L-proline beta-naphthylamide

Supply Marketing:

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

TRC
Z-PRO-BNA
500mg
$ 130.00

Crysdot
(S)-Benzyl2-(naphthalen-2-ylcarbamoyl)pyrrolidine-1-carboxylate 97%
1g
$ 465.00

Chemenu
(S)-Benzyl2-(naphthalen-2-ylcarbamoyl)pyrrolidine-1-carboxylate 97%
1g
$ 439.00

Total 9 raw suppliers

Chemical Property of Z-L-proline beta-naphthylamide

Chemical Property:

PSA：58.64000
LogP:4.59040
Storage Temp.:Store at RT.
XLogP3:4.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:374.16304257
Heavy Atom Count:28
Complexity:546

Purity/Quality:

99% ^*data from raw suppliers

Z-PRO-BNA ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC(N(C1)C(=O)OCC2=CC=CC=C2)C(=O)NC3=CC4=CC=CC=C4C=C3
Isomeric SMILES:C1C[C@H](N(C1)C(=O)OCC2=CC=CC=C2)C(=O)NC3=CC4=CC=CC=C4C=C3

Technology Process of Z-L-proline beta-naphthylamide

There total 4 articles about Z-L-proline beta-naphthylamide 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:

: 1148-11-4
N-Benzyloxycarbonyl-L-proline

: 86925-99-7
(S)-1-benzyloxycarbonyl-N-(2-naphthyl)-2-pyrrolidinecarboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: dicyclohexylcarbodiimide / tetrahydrofuran / 3 h / 0 °C

2: tetrahydrofuran / 1.) 3 h, 0 deg C; 2.) 12 h, r.t.

With dicyclohexyl-carbodiimide; In tetrahydrofuran;