1-(Allyloxy)-3-aminopropan-2-ol

Base Information

• Chemical Name: 1-(Allyloxy)-3-aminopropan-2-ol
• CAS No.: 6967-44-8
• Molecular Formula: C6H13NO2
• Molecular Weight: 131.175
• European Community (EC) Number: 230-178-7
• NSC Number: 68326
• DSSTox Substance ID: DTXSID601280744
• Nikkaji Number: J266.012A
• Mol file: 6967-44-8.mol

Synonyms:1-(Allyloxy)-3-aminopropan-2-ol;6967-44-8;EINECS 230-178-7;1-Allyloxy-3-amino-propan-2-ol;NSC68326;SCHEMBL1563814;1-amino-3-allyloxy-2-propanol;3-Allyloxy-2-hydroxy-propylamine;DTXSID601280744;MFCD00047938;NSC 68326;NSC-68326;AKOS006273516;1-Amino-3-(2-propenyloxy)-2-propanol;1-Amino-3-(2-propen-1-yloxy)-2-propanol;1-AMINO-3-(PROP-2-EN-1-YLOXY)PROPAN-2-OL

Chemical Property of 1-(Allyloxy)-3-aminopropan-2-ol

Chemical Property:

• Vapor Pressure: 0.0139mmHg at 25°C
• Boiling Point: 228.8°C at 760 mmHg
• Flash Point: 92.2°C
• Density: 1.004g/cm³
• XLogP3: -0.8
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 5
• Exact Mass: 131.094628657
• Heavy Atom Count: 9
• Complexity: 75.5

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C=CCOCC(CN)O

Technology Process of 1-(Allyloxy)-3-aminopropan-2-ol

There total 10 articles about 1-(Allyloxy)-3-aminopropan-2-ol 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: 87.0%

4,4'-Dihydroxybenzophenone (611-99-4) + cyclohexanone (108-94-1,11119-77-0,9003-41-2,9075-99-4) → 2,2-bis(4-hydroxyphenyl)methylenecyclohexane (5189-40-2)

Guidance literature:

With titanium(III) chloride; lithium; In 1,2-dimethoxyethane; 1.) room temp., 4 h; 2.) reflux, 13 h;

DOI:10.1016/S0040-4020(01)89809-4

Reference yield: 70.9%

C6H12NO5S(1-)*K(1+) → 3-allyloxy-2-oxy-propylamine (6967-44-8)

Guidance literature:

With hydrogenchloride; 2.) EtOH, reflux;

DOI:10.1007/BF02495401

Reference yield: 46.1%

Allyl glycidyl ether (106-92-3,25639-25-2,90907-93-0) → 3-allyloxy-2-oxy-propylamine (6967-44-8)

Guidance literature:

With ammonium hydroxide; In methanol; water; at 25 ℃;

upstream raw materials:

Allyl glycidyl ether

methyl cyclohexylcarboxylate

(4-bromophenoxy)trimethylsilane

4,4'-Dihydroxybenzophenone

Downstream raw materials:

1-(3-Allyloxy-2-hydroxy-propylamino)-3-(2-methoxy-phenoxy)-propan-2-ol

1-Allyloxy-3-[2-(4-methoxy-phenoxy)-ethylamino]-propan-2-ol

1-Allyloxy-3-(2-o-tolyloxy-ethylamino)-propan-2-ol

1-Allyloxy-3-[2-(2-methoxy-phenoxy)-ethylamino]-propan-2-ol