(+)-(R)-α-methyl-N-(phenylmethyl)benzenepropanamine

Base Information

Chemical Name:(+)-(R)-α-methyl-N-(phenylmethyl)benzenepropanamine
CAS No.:75659-06-2
Molecular Formula:C₁₇H₂₁N
Molecular Weight:239.36
Hs Code.:

Synonyms:(+)-(R)-α-methyl-N-(phenylmethyl)benzenepropanamine

Suppliers and Price of (+)-(R)-α-methyl-N-(phenylmethyl)benzenepropanamine

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
(αR)-α-Methyl-N-(phenylmethyl)benzenepropanamine
5mg
$ 415.00

Medical Isotopes, Inc.
(αR)-α-Methyl-N-(phenylmethyl)benzenepropanamine
25 mg
$ 2125.00

Medical Isotopes, Inc.
(αR)-α-Methyl-N-(phenylmethyl)benzenepropanamine
1 mg
$ 625.00

Total 1 raw suppliers

Chemical Property of (+)-(R)-α-methyl-N-(phenylmethyl)benzenepropanamine

Chemical Property:

Boiling Point:358.6±21.0 °C(Predicted)
Density:0.990±0.06 g/cm3(Predicted)

Purity/Quality:

96%min ^*data from raw suppliers

(αR)-α-Methyl-N-(phenylmethyl)benzenepropanamine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses (αR)-α-Methyl-N-(phenylmethyl)benzenepropanamine is an intermediate in the synthesis of (R,R)-Labetalol (L096500), a specific competitive antagonist at both α-and β-adrenergic receptor sites. (R,R)-Labetalol is used as an antihypertensive.

Technology Process of (+)-(R)-α-methyl-N-(phenylmethyl)benzenepropanamine

There total 17 articles about (+)-(R)-α-methyl-N-(phenylmethyl)benzenepropanamine 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: 86.0%

: (R)-N-(1-methyl-3-phenylpropyl)-benzamide

: 75659-06-2
(+)-(R)-α-methyl-N-(phenylmethyl)benzenepropanamine

Guidance literature:: With lithium aluminium tetrahydride; at 20 ℃;
DOI:10.1016/j.mcat.2018.02.017

Reference yield: 70.0%

: (R(a),S)-4-(1-methyl-3-phenylpropoxy)dinaphtho[2,1-d:1'2'-f][1,3,2]dioxaphosphepin-4-selenide

: 100-46-9
benzylamine

: 75659-06-2
(+)-(R)-α-methyl-N-(phenylmethyl)benzenepropanamine

Guidance literature:: (R(a),S)-4-(1-methyl-3-phenylpropoxy)dinaphtho[2,1-d:1'2'-f][1,3,2]dioxaphosphepin-4-selenide; benzylamine; In tetrahydrofuran; for 15h; Heating;

With sodium hydroxide; In tetrahydrofuran; for 1h; Heating;
DOI:10.1021/ja060308b