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2-AMINO-CYCLOHEX-1-ENECARBOXYLIC ACID ETHYL ESTER

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2-AMINO-CYCLOHEX-1-ENECARBOXYLIC ACID ETHYL ESTER Basic information

Product Name:
2-AMINO-CYCLOHEX-1-ENECARBOXYLIC ACID ETHYL ESTER
Synonyms:
  • ETHYL-(2-AMINOCYCLOHEX-1-EN-1-CARBOXYLAT)
  • ETHYL 2-AMINOCYCLOHEX-1-ENE-1-CARBOXYLATE
  • ETHYL 2-AMINO-1-CYCLOHEXENE-1-CARBOXYLATE
  • 2-AMINO-CYCLOHEX-1-ENECARBOXYLIC ACID ETHYL ESTER
  • Ethyl 2-amino-1-cyclohexene-1-carboxylate,98%
  • 2-Amino-1-cyclohexenecarboxylic acid ethyl ester
  • 1-Cyclohexene-1-carboxylicacid, 2-aMino-, ethyl ester
  • Ethyl 2-aMinocyclohex-1-enecarboxylate
CAS:
1128-00-3
MF:
C9H15NO2
MW:
169.22
Mol File:
1128-00-3.mol
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2-AMINO-CYCLOHEX-1-ENECARBOXYLIC ACID ETHYL ESTER Chemical Properties

Melting point:
70-74 °C
Boiling point:
298.52°C (rough estimate)
Density 
1.0873 (rough estimate)
refractive index 
1.4580 (estimate)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
form 
Crystals or Crystalline Powder
pka
6.97±0.20(Predicted)
color 
White to light yellow
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Safety Information

Safety Statements 
24/25
HS Code 
29224999

MSDS

  • Language:English Provider:ACROS
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2-AMINO-CYCLOHEX-1-ENECARBOXYLIC ACID ETHYL ESTER Usage And Synthesis

Chemical Properties

white to light yellow crystals or

Definition

ChEBI: Ethyl-2-amino-1-cyclohexene-1-carboxylate is an enamine and an enone.

Synthesis

1655-07-8

1128-00-3

a) To a solution of ethyl 2-cyclohexanone carboxylate (18.9 mL, 118 mmol) in methanol (120 mL) was added ammonium carbamate (9.20 g, 118 mmol). The reaction mixture was stirred at room temperature for 1 hour until the ammonium carbamate was completely dissolved. After continuing to stir the reaction mixture for 1 h, the volatile solvent was removed by distillation under reduced pressure to afford ethyl 2-amino-1-cyclohexene-1-carboxylate as a white to pale yellow solid (19.9 g, quantitative yield). The product was characterized by 1H NMR (400 MHz, CDCl3): δ 1.28 (t, J = 7.2 Hz, 3H), 1.57-1.71 (m, 4H), 2.21 (t, J = 6.1 Hz, 2H), 2.26 (t, J = 6.1 Hz, 2H), 4.15 (q, J = 7.2 Hz, 2H), 6.06 (br s, 2H) .

References

[1] Patent: WO2013/26900, 2013, A1. Location in patent: Page/Page column 60
[2] New Journal of Chemistry, 2005, vol. 29, # 6, p. 769 - 772
[3] Tetrahedron Letters, 2013, vol. 54, # 9, p. 1133 - 1136
[4] Bioorganic and Medicinal Chemistry, 2014, vol. 22, # 14, p. 3654 - 3669
[5] Chemistry of Heterocyclic Compounds, 2006, vol. 42, # 6, p. 765 - 775

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