ChemicalBook--->CAS DataBase List--->56545-22-3

56545-22-3

56545-22-3 Structure

56545-22-3 Structure
IdentificationBack Directory
[Name]

H-ABU-OME HCL
[CAS]

56545-22-3
[Synonyms]

L-2-Abu-OMe HCl
H-ABU-OME HCL USP/EP/BP
Methyl L-homoalaninate HCl
Methyl (S)-2-aMinobutanoate HCl
L-2-AMINOBUTYRIC ACID METHYL ESTER HCL
Methyl L-2-aminobutanoate hydrochloride
Methyl (S)-2-aminobutyrate hydrochloride
Methyl (S)-2-aminobutanoate hydrochloride
(S)-2-Aminobutanoic Acid Methyl Ester HCl
(S)-methyl 2-aminobutanoate hydrochloride
Methyl (2S)-2-aminobutanoate hydrochloride
L-α-AMinobutyric Acid Methyl Ester Hydrochloride
L-2-AMinobutyric Acid Methyl Ester Hydrochloride
L-2-Amino butanoic acid methyl ester hydrochloride
(S)-2-AMinobutanoic Acid Methyl Ester Hydrochloride
(S)-2-AMino-butanoic Acid Methyl Ester Hydrochloride
[Molecular Formula]

C5H12ClNO2
[MDL Number]

MFCD09037399
[MOL File]

56545-22-3.mol
[Molecular Weight]

153.607
Chemical PropertiesBack Directory
[Melting point ]

116-117℃
[storage temp. ]

Inert atmosphere,2-8°C
[solubility ]

Aqueous Acid (Sparingly), DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[color ]

White to Off-White
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Uses]

Intermediate in the preparation of Ergonovine (E597800) derivatives.
[Synthesis]

Methanol

67-56-1

BOC-ABU-OH

34306-42-8

DL-2-AMINO-N-BUTYRIC ACID METHYL ESTER HYDROCHLORIDE

7682-18-0

The general procedure for the synthesis of DL-2-aminobutyric acid methyl ester hydrochloride from methanol and Boc-L-2-aminobutyric acid was as follows: 10.0 g (49.2 mmol) of Boc-L-2-aminobutyric acid was dissolved in 100 mL of methanol, and 6 mL (82.2 mmol) of thionyl chloride was added slowly and dropwise at 0 °C. The reaction mixture was stirred at room temperature for 14 h before the solvent was removed by vacuum evaporation. A product of 7.6 g (101% yield) was obtained. The structure of the product was confirmed by electrospray mass spectrometry (ES-MS) and the molecular ion peak (M + H)+ was observed as 118.

[References]

[1] Patent: US2010/144681, 2010, A1. Location in patent: Page/Page column 67
Spectrum DetailBack Directory
[Spectrum Detail]

H-ABU-OME HCL(56545-22-3)1HNMR
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