ChemicalBook--->CAS DataBase List--->535936-86-8

535936-86-8

535936-86-8 Structure

535936-86-8 Structure
IdentificationBack Directory
[Name]

methyl-2-amino-2-cyclopropyla cetate hydrochloride
[CAS]

535936-86-8
[Synonyms]

DL-cyclopropylglycine methyl ester
Methyl a-Amino-cyclopropaneacetate HCl
Methyl (amino)(cyclopropyl)acetate hydrochloride
Methyl 2-Amino-2-cyclopropaneacetatehydrochloride
methyl-2-amino-2-cyclopropyla cetate hydrochloride
methyl 2-amino-2-cyclopropylacetate hydrogen chloride
Amino-cyclopropyl-acetic acid methyl ester hydrochloride
methyl-2-amino-2-cyclopropyla cetate hydrochloride USP/EP/BP
alpha-Aminocyclopropaneacetic acid methyl ester hydrochloride
[Molecular Formula]

C6H11NO2.ClH
[MDL Number]

MFCD12031219
[MOL File]

535936-86-8.mol
[Molecular Weight]

165.619
Chemical PropertiesBack Directory
[storage temp. ]

Inert atmosphere,Room Temperature
[form ]

Solid
[color ]

White to light brown
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H335-H315-H302
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P270-P301+P312-P330-P501-P264-P280-P305+P351+P338-P337+P313P
[HazardClass ]

IRRITANT
[HS Code ]

2922498590
Hazard InformationBack Directory
[Uses]

Methyl 2-amino-2-cyclopropylacetate hydrochloride is a Glycine (HY-Y0966) derivative[1].
[Synthesis]

DL-Cyclopropylglycine

10294-18-5

methyl-2-amino-2-cyclopropyla cetate hydrochloride

535936-86-8

General procedure for the synthesis of methyl 2-amino-2-cyclopropylacetate hydrochloride from DL-cyclopropylglycine: Thionyl chloride (1.3 g, 0.8 mL, 11 mmol) was added slowly and dropwise to a methanol (4.3 mL) solution of DL-cyclopropylglycine (0.50 g, 4.3 mmol) that was cooled to 0°C. The reaction mixture was stirred for 10 minutes and then gradually warmed to room temperature. The reaction mixture was stirred at 0°C for 10 min and then gradually warmed to room temperature. Stirring was continued at room temperature overnight. Upon completion of the reaction, the mixture was concentrated and dried under pressure of 0.5 mmHg at room temperature to afford methyl 2-amino-2-cyclopropylacetate hydrochloride (0.60 g, 85% yield) as a white solid. The product was characterized by 1H NMR (DMSO-d6): δ 0.51-0.69, 1.05-1.17, 3.36-3.39, 3.75, 8.69.

[References]

[1] Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144. DOI:10.1080/10408398.2012.708368
Spectrum DetailBack Directory
[Spectrum Detail]

methyl-2-amino-2-cyclopropyla cetate hydrochloride(535936-86-8)1HNMR
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