2-Phenoxypropylamine

Base Information

• Chemical Name: 2-Phenoxypropylamine
• CAS No.: 6437-49-6
• Molecular Formula: C9H13 N O
• Molecular Weight: 151.208
• Hs Code.: 2922299090
• Mol file: 6437-49-6.mol

Synonyms:2-Phenoxypropylamine;2-phenoxypropan-1-amine;6437-49-6;2-Phenoxypropylamine, HCl;SCHEMBL3160069;UDRPWKSZPLYUMD-UHFFFAOYSA-N;MFCD00128245;STL219889;AKOS005142990;AB03575;NS-01165;CS-0454649;EN300-144469;A867891;J-510239

Chemical Property of 2-Phenoxypropylamine

Chemical Property:

• Vapor Pressure: 0.0378mmHg at 25°C
• Refractive Index: 1.519
• Boiling Point: 240.5°C at 760 mmHg
• PKA: 8.20±0.10(Predicted)
• Flash Point: 99.5°C
• PSA: 44.48000
• Density: 1.004g/cm³
• LogP: 2.12150
• Sensitive.: Air Sensitive
• Water Solubility.: Insoluble in water.
• XLogP3: 1.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 151.099714038
• Heavy Atom Count: 11
• Complexity: 99.7

Purity/Quality:

97% ^*data from raw suppliers

2-Phenoxypropan-1-amine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(CN)OC1=CC=CC=C1
• Uses: 2-Phenoxypropylamine is used as pharmaceutical intermediate.

Technology Process of 2-Phenoxypropylamine

There total 5 articles about 2-Phenoxypropylamine 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:

2-phenoxypropionitrile (6437-44-1) → (R)-2-Phenoxy-1-propylamine (6437-49-6)

Guidance literature:

With sodium hydroxide; In water;

Reference yield:

→ (R)-2-Phenoxy-1-propylamine (6437-49-6)

Guidance literature:

With lithium aluminium tetrahydride; diethyl ether;

DOI:10.1021/ja01523a059

Reference yield:

→ (R)-2-Phenoxy-1-propylamine (6437-49-6)

Guidance literature:

With ammonium hydroxide; nickel; Hydrogenation;

DOI:10.1021/ja01568a048

upstream raw materials:

2-phenoxypropionitrile

2-[2-phenoxypropyl]-1H-isoindole-1,3(2H)-dione

Downstream raw materials:

(2-phenoxy-propyl)-(7⁽⁹⁾H-purin-6-yl)-amine

(7-chloro-1,1-dioxo-1,2(4)-dihydro-1λ⁶-benzo[1,2,4]thiadiazin-3-yl)-(2-phenoxy-propyl)-amine

4-chlorophenylethanamidine

N-(2-phenoxy-propyl)-4-chlorophenylacetamidine p-toluenesulphonate

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