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946511-97-3

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946511-97-3 Structure

946511-97-3 Structure
IdentificationBack Directory
[Name]

(S)-2-ethylbutyl 2-aminopropanoate hydrochloride
[CAS]

946511-97-3
[Synonyms]

Remdesivir-006-S-HCl
Remdesivir-003-S-HCl
Remdesivir Impurity 8
2-Ethylbutyl L-Alaninate HCL
Remdesivir Related Compound 8
L-alanine-2-ethylbutylester.HCl
2-EthylbutylL-alaninatehydrochloride
Radcivir starting material intermediate)
L-Alanine 2-ethylbutyl ester hydrochloride
2-Ethylbutyl 2-aminopropanoate hydrochloride
2-ethylbutyl (S)-2-aminopropanoate hydrochloride
(S)-2-ethylbutyl 2-aminopropanoate hydrochloride
2-ethylbutyl (2S)-2-aminopropanoate hydrochloride
(S) -2-ethylbutyl aminopropionic acid hydrochloride
(S) -2-Ethylbutyl 2-Aminopropanoate HCl Hydrochloride
2-ethylbutyl ((R)-hydroxy(phenoxy)phosphoryl)-L-alaninate
[Molecular Formula]

C9H20ClNO2
[MDL Number]

MFCD32660031
[MOL File]

946511-97-3.mol
[Molecular Weight]

209.71
Questions And AnswerBack Directory
[Synthesis]

Synthetic route of (S)-2-ethylbutyl 2-aminopropanoate hydrochloride

2-Ethylbutyl-L-Boc-alanine ester is obtained by condensation of L-Boc-alanine and 2-ethylbutanol under the action of EDCI and DMAP, and then the Boc protecting agent is removed by hydrogen chloride to obtain (S)-2-ethylbutyl 2-aminopropanoate hydrochloride.

Chemical PropertiesBack Directory
[Melting point ]

77 - 79°C
[storage temp. ]

Hygroscopic, Refrigerator, under inert atmosphere
[solubility ]

DMSO (Slightly), Water (Sparingly)
[form ]

Solid
[color ]

White to Off-White
[Stability:]

Hygroscopic
[InChI]

InChI=1/C9H19NO2.ClH/c1-4-8(5-2)6-12-9(11)7(3)10;/h7-8H,4-6,10H2,1-3H3;1H/t7-;/s3
[InChIKey]

DEAGOVGXNPHPIJ-WMASNCOMNA-N
[SMILES]

C(CC)(CC)COC(=O)[C@@H](N)C.Cl |&1:9,r|
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
[REACH Registrations]

Active
Hazard InformationBack Directory
[Uses]

L-Alanine 2-Ethylbutyl Ester Hydrochloride is used in the synthesis of phosphoramidate prodrug of a pyrrolo[2,1-f][triazin-4-amino] adenine C-nucleoside (GS-5734) for the treatment of ebola and emerging viruses.
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