(2S)-2-amino-N-(4-methoxynaphthalen-2-yl)propanamide

Base Information

Chemical Name:(2S)-2-amino-N-(4-methoxynaphthalen-2-yl)propanamide
CAS No.:4467-67-8
Molecular Formula:C₁₄H₁₆N₂O₂
Molecular Weight:244.293
Hs Code.:2924299090
European Community (EC) Number:636-938-8
DSSTox Substance ID:DTXSID30350888
Nikkaji Number:J673.562B
Wikidata:Q82126970
Mol file:4467-67-8.mol

Synonyms:4467-67-8;(2S)-2-amino-N-(4-methoxynaphthalen-2-yl)propanamide;N-(4-Methoxynaphthalen-2-yl)-L-alaninamide;SCHEMBL7738208;DTXSID30350888;l-alanine-4-methoxy-2-naphthylamide;L-Alanine 4-methoxy-beta-naphthylamide

Suppliers and Price of (2S)-2-amino-N-(4-methoxynaphthalen-2-yl)propanamide

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
L-ALANINE 4-METHOXY-BETA-NAPHTHYLAMIDE 95.00%
25MG
$ 682.05

Total 4 raw suppliers

Chemical Property of (2S)-2-amino-N-(4-methoxynaphthalen-2-yl)propanamide

Chemical Property:

PSA：64.35000
LogP:2.90740
Storage Temp.:−20°C
XLogP3:1.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:244.121177757
Heavy Atom Count:18
Complexity:296

Purity/Quality:

99% ^*data from raw suppliers

L-ALANINE 4-METHOXY-BETA-NAPHTHYLAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xn
Hazard Codes:Xn
Statements: 40
Safety Statements: 22-36

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C(=O)NC1=CC2=CC=CC=C2C(=C1)OC)N
Isomeric SMILES:C[C@@H](C(=O)NC1=CC2=CC=CC=C2C(=C1)OC)N

Technology Process of (2S)-2-amino-N-(4-methoxynaphthalen-2-yl)propanamide

There total 5 articles about (2S)-2-amino-N-(4-methoxynaphthalen-2-yl)propanamide 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:

: 132-86-5
1,3-dihydroxynaphthalene

: 4467-67-8
L-alanine-4-methoxy-2-naphthylamide hydrochloride

Guidance literature:: Multi-step reaction with 5 steps

1: (i) liq. NH₃, (ii) /BRN= 385737/

2: aq. KOH

3: K₂CO₃ / acetone

4: aq. HCl / ethanol

5: (i) ClCO₂Et, (ii) aq. HCl, MeOH

With hydrogenchloride; potassium hydroxide; potassium carbonate; In ethanol; acetone;
DOI:10.1021/jo01017a016

Reference yield:

: 2792-01-0
3-Acetamido-1-methoxy-naphthalin

: 4467-67-8
L-alanine-4-methoxy-2-naphthylamide hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: aq. HCl / ethanol

2: (i) ClCO₂Et, (ii) aq. HCl, MeOH

With hydrogenchloride; In ethanol;
DOI:10.1021/jo01017a016

Reference yield:

: 2896-05-1
3-Acetamino-naphthol-⁽¹⁾

: 4467-67-8
L-alanine-4-methoxy-2-naphthylamide hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: K₂CO₃ / acetone

2: aq. HCl / ethanol

3: (i) ClCO₂Et, (ii) aq. HCl, MeOH

With hydrogenchloride; potassium carbonate; In ethanol; acetone;
DOI:10.1021/jo01017a016