L-Proline beta-naphthylamide hydrochloride

Base Information

Chemical Name:L-Proline beta-naphthylamide hydrochloride
CAS No.:169553-07-5
Molecular Formula:C₁₅H₁₆N₂O*ClH
Molecular Weight:276.766
Hs Code.:
European Community (EC) Number:624-606-5
DSSTox Substance ID:DTXSID20584973

Synonyms:97216-16-5;L-Proline beta-naphthylamide hydrochloride;169553-07-5;L-Proline-2-naphthylamide hydrochloride;(2S)-N-naphthalen-2-ylpyrrolidine-2-carboxamide;hydrochloride;(2S)-N-(naphthalen-2-yl)pyrrolidine-2-carboxamide hydrochloride;H-Pro-bNA HCl;H-Pro-NA HCl;DTXSID20584973;2-Pyrrolidinecarboxamide,N-2-naphthalenyl-, hydrochloride (1:1);MFCD00038937;AKOS024307515;L-Proline 2-naphthylamide hydrochloride;AS-71666;L-Proline beta -naphthylamide hydrochloride;P-7500;L-Proline beta-naphthylamide hydrochloride, >=99%;N-Naphthalen-2-yl-L-prolinamide--hydrogen chloride (1/1);(S)-N-(naphthalen-2-yl)pyrrolidine-2-carboxamide hydrochloride;2-Pyrrolidinecarboxamide,N-2-naphthalenyl-,hydrochloride(1:1)

Suppliers and Price of L-Proline beta-naphthylamide hydrochloride

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

American Custom Chemicals Corporation
(2S)-N-NAPHTHALEN-2-YLPYRROLIDINE-2-CARBOXAMIDE HYDROCHLORIDE 95.00%
1G
$ 211.05

Total 1 raw suppliers

Chemical Property of L-Proline beta-naphthylamide hydrochloride

Chemical Property:

Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:276.1029409
Heavy Atom Count:19
Complexity:305

Purity/Quality:: (2S)-N-NAPHTHALEN-2-YLPYRROLIDINE-2-CARBOXAMIDE HYDROCHLORIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CC(NC1)C(=O)NC2=CC3=CC=CC=C3C=C2.Cl
Isomeric SMILES:C1C[C@H](NC1)C(=O)NC2=CC3=CC=CC=C3C=C2.Cl

Technology Process of L-Proline beta-naphthylamide hydrochloride

There total 2 articles about L-Proline beta-naphthylamide hydrochloride 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:

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

: 169553-07-5,97216-16-5
L-proline β-naphthylamide hydrochloride

Guidance literature:: With hydrogenchloride; methanol; palladium; Hydration;

Reference yield:

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

: 169553-07-5,97216-16-5
L-proline β-naphthylamide hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine; toluene; CHCl₃ / anschliessend Erwaermen mit <2>Naphthylamin

2: palladium; methanol; aqueous HCl / Hydration

With hydrogenchloride; methanol; chloroform; palladium; triethylamine; toluene;