4829-01-0

Basic information

• Product Name: 1-PHENYL-7-OXA-BICYCLO[4.1.0]HEPTANE
• Synonyms: 1-PHENYL-7-OXA-BICYCLO[4.1.0]HEPTANE
• CAS NO: 4829-01-0
• Molecular Formula: C₁₂H₁₄O
• Molecular Weight: 174.23896
• Mol File: 4829-01-0.mol
• Article Data: 211

Chemical Properties

• Melting Point: 115.5 °C
• Boiling Point: 267.7°C at 760 mmHg
• Flash Point: 111.5°C
• Appearance: /
• Density: 1.122g/cm³
• Vapor Pressure: 0.0132mmHg at 25°C
• Refractive Index: 1.58
• CAS DataBase Reference: 1-PHENYL-7-OXA-BICYCLO[4.1.0]HEPTANE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-PHENYL-7-OXA-BICYCLO[4.1.0]HEPTANE(4829-01-0)
• EPA Substance Registry System: 1-PHENYL-7-OXA-BICYCLO[4.1.0]HEPTANE(4829-01-0)

Safety Data

• Hazardous Substances Data: 4829-01-0(Hazardous Substances Data)

Usage

Explanation

1-PHENYL-7-OXA-BICYCLO[4.1.0]HEPTANE consists of 11 carbon atoms, 12 hydrogen atoms, and 1 oxygen atom.
2. Bicyclic organic compound

Explanation

The compound has two cyclic structures within its molecular structure, specifically a heptane ring system and an oxa ring.
3. Heptane ring system

Explanation

One of the cyclic structures in the compound consists of seven carbon atoms arranged in a ring formation.
4. Phenyl group attached

Explanation

A phenyl group, which is a benzene ring with one hydrogen atom replaced by an alkyl group, is attached to the bicyclic structure.
5. Oxa ring

Explanation

The other cyclic structure in the compound is an oxa ring, which is a four-membered ring containing one oxygen atom and three carbon atoms.

Explanation

The compound is also known by this name, which is an alternative way of describing its structure and composition.
7. Used in organic synthesis and research

Explanation

1-PHENYL-7-OXA-BICYCLO[4.1.0]HEPTANE serves as a building block for creating more complex molecules in the field of organic chemistry.
8. Importance in organic chemistry and pharmaceutical research

Explanation

The unique structure and properties of 1-PHENYL-7-OXA-BICYCLO[4.1.0]HEPTANE make it a significant compound for studying and developing new organic and pharmaceutical compounds.

InChI:InChI=1/C12H14O/c1-2-6-10(7-3-1)12-9-5-4-8-11(12)13-12/h1-3,6-7,11H,4-5,8-9H2

Upstream product

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

Downstream Products

• 1444-65-1 (RS)-2-phenylcyclohexanone 
• 21573-69-3 1-phenyl-1-cyclopentanecarboxaldehyde 
• 26524-28-7 phenylcyclohexylacetate 
• 17540-06-6 trans-2-(dimethylamino)-1-phenylcyclohexanol 
• 129920-34-9 (1R^*,2S^*)-2-(methylamino)-1-phenylcyclohexane-1-ol 
• 94824-44-9 1-phenyl-2-piperidin-1-yl-cyclohexanol 
• 101688-13-5 phenyl-2 t-(piperidino-1)-2 r-cyclohexanol 
• 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 
• 114274-98-5 2-phenyl-2-(trimethylsilylethynyl)cyclohexanol 

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