1728-32-1

Basic information

• Product Name: 1,3,5-Cycloheptatriene, 1-methoxy-
• Synonyms: 1,3,5-Cycloheptatriene, 1-methoxy-;1-methoxy-1,3,5-cycloheptatriene
• CAS NO: 1728-32-1
• Molecular Formula: C₈H₁₀O
• Molecular Weight: 122.16
• Product Categories: Miscellaneous Reagents, Pharmaceuticals, Intermediates & Fine Chemicals
• Mol File: 1728-32-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 208.9°Cat760mmHg
• Flash Point: 72.5°C
• Appearance: /
• Density: 0.95g/cm³
• Vapor Pressure: 0.302mmHg at 25°C
• Refractive Index: 1.508
• CAS DataBase Reference: 1,3,5-Cycloheptatriene, 1-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-Cycloheptatriene, 1-methoxy-(1728-32-1)
• EPA Substance Registry System: 1,3,5-Cycloheptatriene, 1-methoxy-(1728-32-1)

Safety Data

• Hazardous Substances Data: 1728-32-1(Hazardous Substances Data)

Usage

Description

1,3,5-Cycloheptatriene, 1-methoxyis an organic compound with the molecular formula C8H10O. It is a derivative of cycloheptatriene, featuring a methoxy group attached to the molecule. 1,3,5-Cycloheptatriene, 1-methoxyis known for its potential mutagenic and carcinogenic properties, making it a subject of interest in various research fields.

Uses

Used in Organic Chemistry:
1,3,5-Cycloheptatriene, 1-methoxyis used as a synthetic intermediate for the production of non-benzenoid aromatic compounds. Its unique structure allows for the creation of various organic molecules with potential applications in different industries, such as pharmaceuticals, materials science, and agrochemicals.
Used in Research:
Due to its clastogenic mutagen properties, 1,3,5-Cycloheptatriene, 1-methoxyis utilized in research studies to understand the mechanisms of DNA damage, mutation, and carcinogenesis. This knowledge can contribute to the development of new strategies for cancer prevention and treatment.

InChI:InChI=1/C8H10O/c1-9-8-6-4-2-3-5-7-8/h2-6H,7H2,1H3

Upstream product

• 186581-53-3 diazomethane 
• 100-66-3 methoxybenzene 
• 1714-40-5 3-methoxy-1,3,5-cycloheptatriene 
• 184-26-9 1,4-dioxaspiro[4.6]undecane 
• 124-41-4 sodium methylate 
• 1714-38-1 7-methoxy-1,3,5-cycloheptatriene 
• 544-25-2 Cyclohepta-1,3,5-triene 

Downstream Products

• 18207-24-4 7,7-dimethoxy-1,3,5-cycloheptatriene 
• 1121-65-9 cyclohepta-3,5-dienone 
• 4636-39-9 4-hydroxy-cycloheptatrienone 
• 135-02-4 ortho-anisaldehyde 
• 539-80-0 Tropone 
• 6621-70-1 methyl ether of γ-tropolone 
• 499-44-5 hinokitiol 
• 55076-49-8 2-amino-6-isopropyl-cycloheptatrienone 
• 108168-72-5 3-isopropylcycloheptanone 
• 13656-81-0 nezukone 
• 34320-91-7 4-Phenyl-tropon 
• 16235-52-2 4-<4-Methoxy-phenyl>-tropon 
• 126893-52-5 7-Isopropyl-3-methoxy-cyclohepta-1,3,5-triene 
• 126893-59-2 4-Isopropyl-1-methoxy-cyclohepta-1,3,5-triene 

Relevant articles and documents

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Anodic oxidation of cycloheptatriene systems and its application to the synthesis of non-benzenoid aromatic compounds

Anodic oxidation of cycloheptatrienes has been found to be one of the most powerful key tools for the preparation of a variety of non-benzenoid aromatic compounds such as tropylium salts, tropones, tropolones, 2H-cyclohepta[b]furan-2-ones, and azulenes.

Novel process for synthesis of a liquid irritant, 1-methoxycycloheptratriene

An improved multi-step process for synthesizing the liquid irritant 1-metycycloheptatriene from tropylium tetrafluoborate the improvement comprising the step of using a polymerization/condensation inhibitor or retarder to minimize impurities and increase yield of the irritant product. Phenothiazine is the preferred polymerization inhibitor.