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CAS 67589-47-3

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Cyclohexanecarboxylic acid, 4-butyl-, 4-ethoxyphenyl ester, trans-

Description:
Cyclohexanecarboxylic acid, 4-butyl-, 4-ethoxyphenyl ester, trans- (CAS 67589-47-3) is an organic compound characterized by its ester functional group, which is formed from the reaction of cyclohexanecarboxylic acid and a phenolic compound. This substance features a cyclohexane ring, which contributes to its cyclic structure and influences its physical properties, such as boiling and melting points. The presence of the butyl and ethoxy groups enhances its hydrophobic characteristics, making it less soluble in water but more soluble in organic solvents. The trans configuration indicates that the substituents are positioned on opposite sides of the ester bond, which can affect the compound's steric interactions and overall stability. This compound may exhibit moderate to low toxicity, typical of many esters, and its applications could range from use in organic synthesis to potential roles in materials science or pharmaceuticals, depending on its reactivity and functional properties. As with all chemical substances, proper handling and safety measures should be observed.
Formula:C19H28O3
InChI:InChI=1/C19H28O3/c1-3-5-6-15-7-9-16(10-8-15)19(20)22-18-13-11-17(12-14-18)21-4-2/h11-16H,3-10H2,1-2H3/t15-,16-
InChI key:InChIKey=JAYBMJPZPJBTQZ-WKILWMFINA-N
SMILES:O(C(=O)[C@H]1CC[C@H](CCCC)CC1)C2=CC=C(OCC)C=C2
Synonyms:
  • 4-Ethoxyphenyl 4-Butylcyclohexanecarboxylate
  • 4-Ethoxyphenyl Trans-4-Butylcyclohexanecarboxylate
  • 4-Ethoxyphenyl trans-4-butylcyclohexane-1-carboxylate
  • 4-Ethoxyphenyl trans-4-butylcyclohexylcarboxylate
  • 4-Ethoxyphenyl trans-4-butylcycolhexanecarboxylate
  • 4-Heb-O2
  • Cyclohexanecarboxylic acid, 4-butyl-, 4-ethoxyphenyl ester, trans-
  • p-Ethoxyphenyl trans-4-butylcyclohexanecarboxylate
  • trans-4-Butyl-(4-ethoxyphenyl)cyclohexanecarboxylate
  • trans-4-Ethoxyphenyl 4-butylcyclohexane-1-carboxylate
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