134750-74-6

Basic information

• Product Name: 1,5-bis(2'-methoxymethoxy-1'-phenylcyclohexyloxy)-3-oxapentane
• CAS NO: 134750-74-6
• Molecular Weight: 542.713
• Mol File: 134750-74-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,5-bis(2'-methoxymethoxy-1'-phenylcyclohexyloxy)-3-oxapentane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,5-bis(2'-methoxymethoxy-1'-phenylcyclohexyloxy)-3-oxapentane(134750-74-6)
• EPA Substance Registry System: 1,5-bis(2'-methoxymethoxy-1'-phenylcyclohexyloxy)-3-oxapentane(134750-74-6)

Safety Data

• Hazardous Substances Data: 134750-74-6(Hazardous Substances Data)

Upstream product

• 34604-52-9 diethylene glycol dimesylate 
• 134750-73-5 (-)-cis-2-(Methoxymethoxy)-1-phenylcyclohexanol 
• 4912-59-8 (1R,2R)-1-phenyl-1,2-cyclohexanediol 
• 4912-59-8 1-phenyl-1,2-cyclohexanediol 
• 23313-43-1 cis-acetic acid 2-hydroxy-2-phenyl-cyclohexyl ester 
• 134780-72-6 (1R,2S)-2-Methoxymethoxy-1-phenyl-cyclohexanol 
• 17540-15-7 (1R,2S)-1-phenyl-1,2-cyclohexanediol 

Downstream Products

• 134750-75-7 2,2'-Oxydiethylenedioxybis(2-phenylcyclohexanol) 
• 134750-75-7 C₂₈H₃₈O₅ 
• 134780-74-8 2,2'-diphenyl-2,2'-dicyclohexanol 
• 169768-33-6 C₃₆H₄₂O₇ 
• 155935-05-0 C₃₈H₄₈O₇ 

Relevant articles and documents

The Synthesis of Azophenolic Crown Ethers of CS Symmetry incorporating cis-1-Phenylcyclohexane-1,2-diol Residues and Diastereotopic Face Selectivity in Complexation of Ethanolamine by their Diastereotopic Faces

Azophenolic crown ethers 9 and 10 of CS symmetry incorporating cis-1-phenylcyclohexane-1,2-diol residues as a steric barrier have been prepared; they bind ethanolamine stereoselectively to one of their diastereotopic faces.

Synthesis and Enantiomer Recognition of Crown Ethers containing Cyclohexane-1,2-diol Derivatives as the Chiral Centre and Enzymatic Resolution of the Chiral Subunits

The cyclohexane-1,2-diol derivatives 1 and 4 of high optical purity have been prepared by enantioselective hydrolysis of their acetates (+/-)-2 and (+/-)-5 using pig liver esterase.The enantiomer recognition behaviour of the chiral crown ethers 11, 14, 15