1,2-Dimethylpropylamine hydrochloride

Base Information

Chemical Name:1,2-Dimethylpropylamine hydrochloride
CAS No.:758-27-0
Molecular Formula:C₅H₁₃N*ClH
Molecular Weight:123.626
Hs Code.:
DSSTox Substance ID:DTXSID30997191

Synonyms:1,2-Dimethylpropylamine hydrochloride;758-27-0;(R)-(-)-2-Amino-3-methylbutane hydrochloride;3-Methyl-2-aminobutane hydrochloride;2-Butanamine, 3-methyl-, hydrochloride;Propylamine, 1,2-dimethyl-, hydrochloride;(S)-(+)-2-Amino-3-methylbutane hydrochloride;SCHEMBL6267532;DTXSID30997191;RBOBXILUTBVQOQ-UHFFFAOYSA-N;3-methylbutan-2-amine;hydrochloride;MFCD28501706;SB13414;SB13416;SY059202;3-Methylbutan-2-amine--hydrogen chloride (1/1);2-Butanamine, 3-methyl-, hydrochloride (1:1), (2R)-;2-Butanamine, 3-methyl-, hydrochloride (1:1), (2S)-

Suppliers and Price of 1,2-Dimethylpropylamine 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
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price

Total 1 raw suppliers

Chemical Property of 1,2-Dimethylpropylamine hydrochloride

Chemical Property:

Vapor Pressure:69.2mmHg at 25°C
Boiling Point:85.5°Cat760mmHg
Flash Point:°C
PSA：26.02000
Density:g/cm³
LogP:2.49190
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:123.0814771
Heavy Atom Count:7
Complexity:32.9

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)C(C)N.Cl

Technology Process of 1,2-Dimethylpropylamine hydrochloride

There total 14 articles about 1,2-Dimethylpropylamine 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: 94.0%

: 866993-51-3
(R)-N-(3-methylbutan-2-ylidene)-2-methylpropane-2-sulfinamide

: 758-27-0,31519-52-5,31519-53-6
(R)-1,2-dimethylpropylamine hydrochloride

Guidance literature:: (R)-N-(3-methylbutan-2-ylidene)-2-methylpropane-2-sulfinamide; With [RhCl₂(p-cymene)]2; potassium tert-butylate; 2-Amino-2-methyl-1-propanol; isopropyl alcohol; at 50 ℃; for 0.5h; Inert atmosphere; Microwave irradiation; Molecular sieve;

With hydrogenchloride; In diethyl ether; enantioselective reaction; Inert atmosphere;
DOI:10.1002/ejoc.201402884

Reference yield: 89.0%

: 293305-73-4
tert-butyl (1R)-1,2-dimethylpropyl carbamate

: 758-27-0,31519-52-5,31519-53-6
(R)-1,2-dimethylpropylamine hydrochloride

Guidance literature:: tert-butyl (1R)-1,2-dimethylpropyl carbamate; With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 18h;

With hydrogenchloride; In diethyl ether; chloroform; Further stages.;
DOI:10.1021/jo000242h

Reference yield: 50.0%

: ClH*C₅H₁₃N*H₃N

: 758-27-0,31519-52-5,31519-53-6
(R)-1,2-dimethylpropylamine hydrochloride

Guidance literature:: ClH*C₅H₁₃N*H₃N; In methanol; dichloromethane;

With hydrogenchloride; In water; at 20 ℃; for 1h;
DOI:10.1002/anie.201504554