Basic information Safety Supplier Related

TRANS-4-AMINOCYCLOHEXANE CARBOXYLIC ACID ETHYL ESTER

Basic information Safety Supplier Related

TRANS-4-AMINOCYCLOHEXANE CARBOXYLIC ACID ETHYL ESTER Basic information

Product Name:
TRANS-4-AMINOCYCLOHEXANE CARBOXYLIC ACID ETHYL ESTER
Synonyms:
  • TRANS-4-AMINOCYCLOHEXANE CARBOXYLIC ACID ETHYL ESTER
  • (trans-4-Carboethoxycyclohexyl)amine
  • Ethyl trans-4-Aminocyclohexanecarboxylate
  • Cyclohexanecarboxylicacid,4-aMino-,ethylester,trans-
  • (1s,4s)-ethyl 4-aminocyclohexanecarboxylate
  • trans-Ethyl 4-aminocyclohexanecarboxylate
  • Ethyl trans-4-aminocyclohexane-1-carboxylate
CAS:
1678-68-8
MF:
C9H17NO2
MW:
171.24
Product Categories:
  • Chemical Amines
  • Amines
Mol File:
1678-68-8.mol
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TRANS-4-AMINOCYCLOHEXANE CARBOXYLIC ACID ETHYL ESTER Chemical Properties

Boiling point:
139-140℃ (13 Torr)
Density 
1.018±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
10.36±0.70(Predicted)
Appearance
Light yellow to yellow Liquid
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TRANS-4-AMINOCYCLOHEXANE CARBOXYLIC ACID ETHYL ESTER Usage And Synthesis

Chemical Properties

Yellow Solid

Synthesis

64-17-5

27960-59-4

1678-68-8

General procedure for the synthesis of ethyl trans-4-aminocyclohexanecarboxylate from ethanol and trans-4-aminocyclohexanecarboxylic acid hydrochloride: 1. concentrated hydrochloric acid (7 mL) was added to a suspension of (1r,4r)-4-aminocyclohexanecarboxylic acid hydrochloride (6.32 g, 0.035 mol) in ethanol (100 mL) and the mixture was stirred. 2. The mixture was heated to 60 °C and the reaction was kept overnight. 3. Upon completion of the reaction, the mixture was evaporated under vacuum to remove the solvent. 4. The residue was thoroughly removed from water by azeotropy with water, followed by azeotropy with ethanol and finally azeotropy with toluene to afford the title product ethyl trans-4-aminocyclohexanecarboxylate as a white solid (7.2 g, 98% yield). 5. The structure of the product was determined by 1H2O2 analysis. 5. The structure of the product was confirmed by 1H NMR (300 MHz, DMSO-d6): δ 4.05 (q, J = 7.1 Hz, 2H), 2.95 (bs, 1H), 2.30-2.15 (m, 1H), 2.02-1.88 (m, 4H), 1.43-1.28 (m, 4H), 1.22-1.13 (t, J = 6.9 Hz, 3H). Hz, 3H).

References

[1] Patent: WO2016/46390, 2016, A1. Location in patent: Page/Page column 44
[2] Journal of Medicinal Chemistry, 2013, vol. 56, # 22, p. 9199 - 9221

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