enzenepropanol, g-aMino-2-Methyl-

Base Information

Chemical Name:enzenepropanol, g-aMino-2-Methyl-
CAS No.:21464-52-8
Molecular Formula:C10H15NO
Molecular Weight:165.235
Hs Code.:
Mol file:21464-52-8.mol

Synonyms:enzenepropanol, g-aMino-2-Methyl-;γ-AMino-2-Methylbenzenepropanol;3-AMINO-3-(2-METHYLPHENYL)PROPAN-1-OL

Suppliers and Price of enzenepropanol, g-aMino-2-Methyl-

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

TRC
γ-Amino-2-methylbenzenepropanol
2.5g
$ 1320.00

AK Scientific
3-Amino-3-(2-methylphenyl)propan-1-ol
2.5g
$ 1988.00

Total 7 raw suppliers

Chemical Property of enzenepropanol, g-aMino-2-Methyl-

Chemical Property:

Boiling Point:155 °C (8 mmHg)
PSA：46.25000
LogP:2.07750

Purity/Quality:

99% ^*data from raw suppliers

γ-Amino-2-methylbenzenepropanol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses γ-Amino-2-methylbenzenepropanol can be used in the synthesis of potential antitumor agents, such as 4-arylcyclophosphamides. γ-Amino-2-methylbenzenepropanol, can be used in the synthesis of potential antitumor agents, such as 4-arylcyclophosphamides.

Technology Process of enzenepropanol, g-aMino-2-Methyl-

There total 4 articles about enzenepropanol, g-aMino-2-Methyl- 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:

: 529-20-4
2-methylphenyl aldehyde

: 21464-52-8
3-amino-3-(2-methylphenyl)propan-1-ol

Guidance literature:: Multi-step reaction with 2 steps

1: ammonium acetate / ethanol / 16 h / Heating

2: LAH / tetrahydrofuran

With ammonium acetate; lithium aluminium tetrahydride; In tetrahydrofuran; ethanol;
DOI:10.1016/j.bmcl.2005.05.038