ChemicalBook--->CAS DataBase List--->72784-43-1

72784-43-1

72784-43-1 Structure

72784-43-1 Structure
IdentificationBack Directory
[Name]

Methyl 1-Aminocyclopropanecarboxylate
[CAS]

72784-43-1
[Synonyms]

ACPCM
Methyl 1-Aminocyclopropanecarboxylate
Methyl 1-amino-1-cyclopropylcarboxylate
Methyl 1-aminocyclopropane-1-carboxylate
Methyl 1-Aminocyclopropanecarboxylate USP/EP/BP
Cyclopropanecarboxylic acid, 1-aMino-, Methyl ester
[Molecular Formula]

C5H9NO2
[MDL Number]

MFCD00906963
[MOL File]

72784-43-1.mol
[Molecular Weight]

115.13
Chemical PropertiesBack Directory
[Boiling point ]

136℃
[density ]

1.188
[Fp ]

12℃
[storage temp. ]

Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
[form ]

liquid
[pka]

6.01±0.20(Predicted)
[color ]

Light yellow
Safety DataBack Directory
[HS Code ]

2921309990
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 1-Aminocyclopropanecarboxylate(72784-43-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methanol

67-56-1

1-Aminocyclopropanecarboxylic acid

22059-21-8

Methyl 1-Aminocyclopropanecarboxylate

72784-43-1

Sulfoxide chloride (8.8 g, 75.1 mmol) was slowly added dropwise to methanol (50 mL) at 0 °C, followed by a one-time addition of 1-aminocyclopropanecarboxylic acid (5.0 g, 49.8 mmol). The reaction mixture was heated to reflux for 1 to 3 hours. Upon completion of the reaction, the solvent was removed by concentration under reduced pressure to afford methyl 1-aminocyclopropanecarboxylate hydrochloride (5.8 g, 100% yield).

[References]

[1] Patent: WO2011/69063, 2011, A2. Location in patent: Page/Page column 84
[2] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 10, p. 2785 - 2788
[3] Patent: US2016/24031, 2016, A1. Location in patent: Paragraph 0598
[4] Bulletin of the Chemical Society of Japan, 1986, vol. 59, # 9, p. 2839 - 2842
[5] Bioorganic and Medicinal Chemistry, 2007, vol. 15, # 10, p. 3345 - 3355
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