3-Aminobutan-2-one hydrochloride

Base Information

• Chemical Name: 3-Aminobutan-2-one hydrochloride
• CAS No.: 21419-24-9
• Molecular Formula: C₄H₉NO*ClH
• Molecular Weight: 123.582
• European Community (EC) Number: 808-672-4

Synonyms:3-aminobutan-2-one hydrochloride;21419-24-9;3-Amino-2-butanone hydrochloride;3-aminobutan-2-one;hydrochloride;MFCD16619121;SCHEMBL6295547;WAA41924;AKOS006237676;SB45084;BS-52339;SY059306;CS-0105630;EN300-91235;D76571;A883620;F1967-1159;Z1263529525

Chemical Property of 3-Aminobutan-2-one hydrochloride

Chemical Property:

• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 123.0450916
• Heavy Atom Count: 7
• Complexity: 60.6

Purity/Quality:

97% ^*data from raw suppliers

3-Amino-2-butanone hydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC(C(=O)C)N.Cl

Technology Process of 3-Aminobutan-2-one hydrochloride

There total 6 articles about 3-Aminobutan-2-one 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: 85.0%

3-nitrobutan-2-one (13058-70-3,521087-47-8,521087-49-0) → 3-Amino-2-butanone hydrochloride (21419-24-9)

Guidance literature:

With hydrogen; sulfided platinum on carbon; In hydrogenchloride; ethanol; at 50 ℃; for 6h; under 760 Torr;

DOI:10.1016/S0040-4039(00)85319-8

Reference yield: 75.0%

(+/-)-2-benzamido-3-butanone (18227-62-8) → 3-Amino-2-butanone hydrochloride (21419-24-9)

Guidance literature:

With hydrogenchloride; In methanol; for 10h; Heating;

DOI:10.1021/jm970189y

Reference yield: 70.0%

2-Ethyl-2,4,5-trimethyl-2,5-dihydro-1H-imidazole (102872-58-2) → 3-Amino-2-butanone hydrochloride (21419-24-9)

Guidance literature:

With hydrogenchloride; at 40 ℃;

DOI:10.1021/jo00126a027

upstream raw materials:

3-nitrobutan-2-one

2-Ethyl-2,4,5-trimethyl-2,5-dihydro-1H-imidazole

(+/-)-2-benzamido-3-butanone

2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione

Downstream raw materials:

Tetramethylpyrazine

3-(2,2-dimethoxyethylamino)-2H-1,4-benzoxazin-2-one

5-chloro-6-(2,6-dichlorophenyl)-3-(1-methyl-2-oxopropylamino)-2H-1,4-oxazin-2-one

3-N-Tritylamino-butanon-⁽²⁾

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