5775-23-5

Basic information

• Product Name: 7-Oxabicyclo[4.1.0]heptane, 1-phenyl-, (1S,6S)-
• CAS NO: 5775-23-5
• Molecular Formula: C12H14O
• Molecular Weight: 174.243
• Mol File: 5775-23-5.mol
• Article Data: 211

Chemical Properties

• CAS DataBase Reference: 7-Oxabicyclo[4.1.0]heptane, 1-phenyl-, (1S,6S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 7-Oxabicyclo[4.1.0]heptane, 1-phenyl-, (1S,6S)-(5775-23-5)
• EPA Substance Registry System: 7-Oxabicyclo[4.1.0]heptane, 1-phenyl-, (1S,6S)-(5775-23-5)

Safety Data

• Hazardous Substances Data: 5775-23-5(Hazardous Substances Data)

Upstream product

• 19324-77-7 (+/-)-2c-chloro-1r-phenyl-cyclohexanol-⁽¹⁾ 
• 771-98-2 1-Phenylcyclohexene 
• 937-14-4 3-chloro-benzenecarboperoxoic acid 
• 108-86-1 bromobenzene 
• 7722-84-1 dihydrogen peroxide 
• 100-58-3 phenylmagnesium bromide 
• 108-94-1 cyclohexanone 
• 40940-63-4 1-phenyl-2-bromo-1-hydroxycyclohexane 
• 1589-60-2 1-phenylcyclohexanol 
• 827-52-1 1-phenyl-1-cyclohexane 
• 75-91-2 tert.-butylhydroperoxide 
• 67-56-1 methanol 
• 93-59-4 Perbenzoic acid 

Downstream Products

• 1444-65-1 (RS)-2-phenylcyclohexanone 
• 21573-69-3 1-phenyl-1-cyclopentanecarboxaldehyde 
• 5422-88-8 phenyl cyclopentyl ketone 
• 69257-64-3 (1R,2R)-2-Methoxy-2-phenyl-cyclohexanol 
• 69257-64-3 (1S,2R)-2-Methoxy-2-phenyl-cyclohexanol 
• 69257-64-3 2-methoxy-2-phenylcyclohexanol 
• 66984-23-4 (+/-)-(1R,2S)-1-methyl-2-hydroxy-1-cyclohexanecarbonitrile 
• 137422-10-7 (1R,2S)-2-Hydroxy-2-phenyl-cyclohexanecarbonitrile 
• 17540-06-6 trans-2-(dimethylamino)-1-phenylcyclohexanol 
• 129920-34-9 (1R^*,2S^*)-2-(methylamino)-1-phenylcyclohexane-1-ol 
• 114274-98-5 2-phenyl-2-(trimethylsilylethynyl)cyclohexanol 
• 1589-60-2 1-phenylcyclohexanol 
• 1444-64-0 2-phenylcyclohexanol 
• 4556-09-6 2-phenylcyclohex-2-enone 

Relevant articles and documents

A new and efficient methodology for olefin epoxidation catalyzed by supported cobalt nanoparticles

A new heterogeneous catalytic system consisting of cobalt nanoparticles (CoNPs) supported on MgO and tert-butyl hydroperoxide (TBHP) as oxidant is presented. This CoNPs@MgO/t-BuOOH catalytic combination allowed the epoxidation of a variety of olefins with good to excellent yield and high selectivity. The catalyst preparation is simple and straightforward from commercially available starting materials and it could be recovered and reused maintaining its unaltered high activity.

RUTHENIUM COMPLEX AND PRODUCTION METHOD THEREOF, CATALYST, AND PRODUCTION METHOD OF OXYGEN-CONTAINING COMPOUND

PROBLEM TO BE SOLVED: To provide a ruthenium complex that is particularly useful as a catalyst for oxidizing a substrate having a carbon-hydrogen bond. SOLUTION: The ruthenium complex represented by the general formula (i) or a cis conformer thereof is provided. In the general formula (i), R1 represents H, a phenyl group or a substituted phenyl group; R2 represents H, a phenyl group or an alkyl group; L1 represents halogen or water molecule; L2 represents triphenylphosphine, pyridine, imidazole or dimethylsulfoxide; X represents halogen; and n represents 1 or 2. SELECTED DRAWING: None COPYRIGHT: (C)2021,JPO&INPIT

Lamellar porous mo-modified carbon nitride polymers photocatalytic epoxidation of olefins

A lamellar porous Mo-modified carbon nitride polymers (CN-Mo) was successfully prepared by a simple bottom-up method, which involves molecule self-assembly by hydrogen bonding between uracil and melamine. Analysis Results of X-ray diffraction (XRD), scann