Basic information Safety Supplier Related

Methyl cis-4-Aminocyclohexanecarboxylate Hydrochloride

Basic information Safety Supplier Related

Methyl cis-4-Aminocyclohexanecarboxylate Hydrochloride Basic information

Product Name:
Methyl cis-4-Aminocyclohexanecarboxylate Hydrochloride
Synonyms:
  • Methyl cis-4-Aminocyclohexanecarboxylate Hydrochloride
  • Nsc145143
  • cis-Methyl 4-aMinocyclohexanecarboxylate hydrochloride
  • cis-4-amino-cyclohexanecarboxylic methyl ester, hydrochloride
  • Methyl cis-4-aminocyclohexanecarboxylate HCl
  • H-1,4-cis-ACHC-OMe Hydrochloride
  • Methyl cis-4-Aminocyclohexanecarboxylate Hydrochloride
  • (1S,4S)-Methyl 4-aminocyclohexanecarboxylate hydrochloride
CAS:
61367-16-6
MF:
C8H15NO2.ClH
MW:
193.672
Mol File:
61367-16-6.mol
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Methyl cis-4-Aminocyclohexanecarboxylate Hydrochloride Chemical Properties

Melting point:
188°C(lit.)
storage temp. 
Inert atmosphere,Room Temperature
form 
powder to crystal
color 
White to Almost white
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Safety Information

HS Code 
2922498590
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Methyl cis-4-Aminocyclohexanecarboxylate Hydrochloride Usage And Synthesis

Chemical Properties

White crystalline powder

Uses

Methyl cis-4-aminocyclohexanecarboxylate HCl

Synthesis

67-56-1

1776-53-0

61367-07-5

Step A: Preparation of methyl trans-4-aminocyclohexanecarboxylate hydrochloride. Trans-4-aminocyclohexanecarboxylic acid (200 mg, 1.40 mmol) was suspended in methanol (5.5 mL) and cooled to -10 °C. Thionyl chloride (204 μL, 2.79 mmol) was added dropwise under stirring and the reaction mixture was stirred at -10 °C for 15 min. Subsequently, the reaction system was slowly warmed to room temperature and stirring was continued for 15 min, after which it was heated to reflux for 1 hr. After completion of the reaction, the reaction was cooled to room temperature and the reaction mixture was concentrated under reduced pressure to afford the white solid product methyl trans-4-aminocyclohexanecarboxylate hydrochloride (260 mg, 96.1% yield). Mass spectral analysis (APCI) showed m/z = 158.0 ([M+H]+).

References

[1] Patent: WO2011/6074, 2011, A1. Location in patent: Page/Page column 95

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