Benzylamine, o-methyl--alpha--propyl- (5CI)

Base Information

Chemical Name:Benzylamine, o-methyl--alpha--propyl- (5CI)
CAS No.:855278-36-3
Molecular Formula:C₁₁H₁₇N
Molecular Weight:163.263
Hs Code.:
Mol file:855278-36-3.mol

Synonyms:Benzylamine,o-methyl-a-propyl- (5CI)

Suppliers and Price of Benzylamine, o-methyl--alpha--propyl- (5CI)

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
[2-(2-methylpropyl)phenyl]methanamine
50mg
$ 240.00

Total 2 raw suppliers

Chemical Property of Benzylamine, o-methyl--alpha--propyl- (5CI)

Chemical Property:

Purity/Quality:

97% ^*data from raw suppliers

[2-(2-methylpropyl)phenyl]methanamine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Benzylamine, o-methyl--alpha--propyl- (5CI)

There total 5 articles about Benzylamine, o-methyl--alpha--propyl- (5CI) 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: 95.0%

: 698377-72-9
(2R)-2-{[(1R)-1-(2-methylphenyl)-3-butenyl]amino}-2-phenylethanamide

: 1213497-62-1,698378-41-5,855278-36-3
(1R)-1-butyl-1-(2-methylphenyl)amine

Guidance literature:: With hydrogen; palladium on activated charcoal; In water; acetic acid; isopropyl alcohol; at 20 ℃; for 120h;
DOI:10.1002/ejoc.200300662

Reference yield:

: 529-20-4
2-methylphenyl aldehyde

: 1213497-62-1,698378-41-5,855278-36-3
(1R)-1-butyl-1-(2-methylphenyl)amine

Guidance literature:: Multi-step reaction with 3 steps

1: CH₂Cl₂ / 20 °C

2: 93 percent / tetrahydrofuran / 0 - 20 °C

3: 95 percent / H₂ / Pd/C / propan-2-ol; H₂O; acetic acid / 120 h / 20 °C

With hydrogen; palladium on activated charcoal; In tetrahydrofuran; dichloromethane; water; acetic acid; isopropyl alcohol;
DOI:10.1002/ejoc.200300662

Reference yield:

: 741681-31-2
(2R)-2-{[(E)-(2-methylphenyl)methylidene]amino}-2-phenylacetamide

: 1213497-62-1,698378-41-5,855278-36-3
(1R)-1-butyl-1-(2-methylphenyl)amine

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / tetrahydrofuran / 0 - 20 °C

2: 95 percent / H₂ / Pd/C / propan-2-ol; H₂O; acetic acid / 120 h / 20 °C

With hydrogen; palladium on activated charcoal; In tetrahydrofuran; water; acetic acid; isopropyl alcohol;
DOI:10.1002/ejoc.200300662