3-(Naphthalen-1-yloxy)propan-1-amine

Base Information

Chemical Name:3-(Naphthalen-1-yloxy)propan-1-amine
CAS No.:58477-93-3
Molecular Formula:C13H15NO
Molecular Weight:201.26400
Hs Code.:2922299090
ChEMBL ID:CHEMBL342704
DSSTox Substance ID:DTXSID30561710
Nikkaji Number:J896.271E
Wikidata:Q82445564
Mol file:58477-93-3.mol

Synonyms:3-(Naphthalen-1-yloxy)propan-1-amine;58477-93-3;3-naphthalen-1-yloxypropan-1-amine;CHEMBL342704;3-(Naphthalen-1-yloxy)propylamine;SCHEMBL7206887;DTXSID30561710;AMY32291;3-(Naphthalen-1-yloxy)-propylamine;BDBM50061972;AKOS000147834;CCG-295952;SB78227;NCGC00323766-01;3-[(Naphthalen-1-yl)oxy]propan-1-amine;EN300-58618;AB01318630-02;AB01318630-03;A869439

Suppliers and Price of 3-(Naphthalen-1-yloxy)propan-1-amine

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

SynChem
3-(Naphthalen-1-yloxy)propylamine 95+%
1 g
$ 250.00

Crysdot
3-(Naphthalen-1-yloxy)propan-1-amine 95+%
5g
$ 589.00

American Custom Chemicals Corporation
1-(3-AMINOPROPOXY)NAPHTHALENE 95.00%
5MG
$ 496.87

Alichem
3-(Naphthalen-1-yloxy)propan-1-amine
5g
$ 735.00

Total 9 raw suppliers

Chemical Property of 3-(Naphthalen-1-yloxy)propan-1-amine

Chemical Property:

PSA：35.25000
LogP:3.26770
Storage Temp.:2-8°C
XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:201.115364102
Heavy Atom Count:15
Complexity:183

Purity/Quality:

97% ^*data from raw suppliers

3-(Naphthalen-1-yloxy)propylamine 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C=CC=C2OCCCN

Technology Process of 3-(Naphthalen-1-yloxy)propan-1-amine

There total 2 articles about 3-(Naphthalen-1-yloxy)propan-1-amine 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: 90.0%

: 102196-49-6
2-[3-(naphthalen-1-yloxy)propyl]-1H-isoindole-1,3(2H)-dione

: 58477-93-3
Desisopropydeoxypropranolol

Guidance literature:: With hydrazine hydrate; In ethanol; for 3h; Heating;
DOI:10.1021/jm00128a039

Reference yield:

: 90-15-3
α-naphthol

: 58477-93-3
Desisopropydeoxypropranolol

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / 1) NaOMe / 1) MeOH, 15 min, 2) DMF, 8 h, reflux

2: 90 percent / aq. N₂H₄*H₂O / ethanol / 3 h / Heating

With sodium methylate; hydrazine hydrate; In ethanol;
DOI:10.1021/jm00128a039