(S)-1-(o-Tolyl)butan-1-amine hydrochloride

Base Information

Chemical Name:(S)-1-(o-Tolyl)butan-1-amine hydrochloride
CAS No.:1213497-62-1
Molecular Formula:C₁₁H₁₇N
Molecular Weight:163.263
Hs Code.:
DSSTox Substance ID:DTXSID80704195
Mol file:1213497-62-1.mol

Synonyms:(S)-1-(o-Tolyl)butan-1-amine hydrochloride;1213497-62-1;(1S)-1-(2-METHYLPHENYL)BUTYLAMINE-HCl;1391437-28-7;(1s)-1-(2-methylphenyl)butylamine HCl;(1S)-1-(2-methylphenyl)butan-1-amine;hydrochloride;(1S)-1-(2-methylphenyl)butan-1-amine hydrochloride;DTXSID80704195;MFCD12757106;(S)-1-(o-Tolyl)butan-1-amine HCl;AKOS015923101;BS-49814;(S)-1-(o-Tolyl)butan-1-aminehydrochloride;CS-0196744;(1s)-1-(2-methylphenyl)butylamine hydrochloride;(1S)-1-(2-Methylphenyl)butan-1-amine--hydrogen chloride (1/1)

Suppliers and Price of (S)-1-(o-Tolyl)butan-1-amine hydrochloride

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

American Custom Chemicals Corporation
(S)-1-(ORTHO-TOLYL)BUTAN-1-AMINE HYDROCHLORIDE 95.00%
5G
$ 2317.35

American Custom Chemicals Corporation
(S)-1-(ORTHO-TOLYL)BUTAN-1-AMINE HYDROCHLORIDE 95.00%
5MG
$ 501.36

Total 14 raw suppliers

Chemical Property of (S)-1-(o-Tolyl)butan-1-amine hydrochloride

Chemical Property:

PSA：26.02000
LogP:4.29720
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:199.1127773
Heavy Atom Count:13
Complexity:122

Purity/Quality:

99%, ^*data from raw suppliers

(S)-1-(ORTHO-TOLYL)BUTAN-1-AMINE HYDROCHLORIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCC(C1=CC=CC=C1C)N.Cl
Isomeric SMILES:CCC[C@@H](C1=CC=CC=C1C)N.Cl

Technology Process of (S)-1-(o-Tolyl)butan-1-amine hydrochloride

There total 5 articles about (S)-1-(o-Tolyl)butan-1-amine 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: 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