(-)-3-(p-Tolyl)-4-aminobutyric acid hydrochloride

Base Information

Chemical Name:(-)-3-(p-Tolyl)-4-aminobutyric acid hydrochloride
CAS No.:67112-58-7
Molecular Formula:C₁₁H₁₅NO₂*ClH
Molecular Weight:229.707
Hs Code.:

Synonyms:(-)-3-(p-Tolyl)-4-aminobutyric acid hydrochloride;Butyric acid, 4-amino-3-(p-tolyl)-, hydrochloride, (-)-;67112-58-7;LS-47845

Suppliers and Price of (-)-3-(p-Tolyl)-4-aminobutyric acid hydrochloride

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of (-)-3-(p-Tolyl)-4-aminobutyric acid hydrochloride

Chemical Property:

Vapor Pressure:2.33E-05mmHg at 25°C
Boiling Point:345.5°Cat760mmHg
Flash Point:162.7°C
Density:g/cm³
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:229.0869564
Heavy Atom Count:15
Complexity:186

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)C(CC(=O)O)CN.Cl
Isomeric SMILES:CC1=CC=C(C=C1)[C@H](CC(=O)O)CN.Cl

Technology Process of (-)-3-(p-Tolyl)-4-aminobutyric acid hydrochloride

There total 7 articles about (-)-3-(p-Tolyl)-4-aminobutyric acid hydrochloride 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: 92.0%

: C₁₂H₁₃N₃O₃

: 67112-58-7,67112-59-8,28311-37-7,67063-80-3
(±)-tolibut hydrochloride

Guidance literature:: C₁₂H₁₃N₃O₃; In tetrahydrofuran; at 60 ℃; for 3h; Inert atmosphere;

With hydrogenchloride; In tetrahydrofuran; water; at 20 ℃; for 1.5h; Inert atmosphere;
DOI:10.1002/chem.202003280