92862-65-2

Basic information

• Product Name: 1-(2-methoxyphenyl)cycloheptene
• CAS NO: 92862-65-2
• Molecular Formula: C₁₄H₁₈O
• Molecular Weight: 202.2921
• Mol File: 92862-65-2.mol

Chemical Properties

• Boiling Point: 314.7°C at 760 mmHg
• Flash Point: 123.3°C
• Density: 0.993g/cm³
• Vapor Pressure: 0.000847mmHg at 25°C
• Refractive Index: 1.53
• CAS DataBase Reference: 1-(2-methoxyphenyl)cycloheptene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-methoxyphenyl)cycloheptene(92862-65-2)
• EPA Substance Registry System: 1-(2-methoxyphenyl)cycloheptene(92862-65-2)

Safety Data

• Hazardous Substances Data: 92862-65-2(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
1-(2-methoxyphenyl)cycloheptene is utilized as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with diverse properties and potential applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(2-methoxyphenyl)cycloheptene serves as a valuable compound for drug development. Its structural features and chemical properties make it a promising candidate for the design and synthesis of novel therapeutic agents.
Used in Material Science:
1-(2-methoxyphenyl)cycloheptene's unique properties also make it a candidate for the development of new materials with specific characteristics, such as improved stability, reactivity, or selectivity, which can be applied in various industrial processes.

Upstream product

• 16750-63-3 2-methoxyphenylmagnesium bromide 
• 502-42-1 cycloheptanone 
• 628-92-2 Cycloheptene 
• 59099-58-0 2-methoxyphenyl triflate 
• 90-05-1 2-methoxy-phenol 

Downstream Products

• 75120-07-9 2-cycloheptylphenol 

Relevant articles and documents

Achieving vinylic selectivity in Mizoroki-heck reaction of cyclic olefins

In Heck reactions of cyclic olefins, the products usually have aryl groups that end up at the allylic and/or homoallylic position. We herein report new selectivity that adds aryl groups to the vinylic position. Cyclic olefins of various ring size worked well. The desired isomers were produced by palladium-hydride-catalyzed isomerization of the initial products. Thus, a specific catalyst must be used so that it can perform two jobs under one set of reaction conditions. Copyright

Well-defined air-stable palladium HASPO complexes for efficient Kumada-Corriu cross-couplings of (Hetero)aryl or alkenyl tosylates

Palladium complexes of representative heteroatom-substituted secondary phosphine oxide (HASPO) preligands were synthesized and fully characterized, including X-ray crystal structure analysis. Importantly, these well-defined complexes served as highly efficient catalysts for Kumada-Corriu cross-coupling reactions of aryl, alkenyl, and even heteroaryl tosylates. Particularly, an air-stable catalyst derived from inexpensive PinP(O)H displayed a remarkably high catalytic efficacy, which resulted in cross-couplings at low catalyst loadings under exceedingly mild reaction conditions with ample scope.