24347-65-7

Basic information

• Product Name: (6-nitrocyclohex-3-en-1-yl)benzene
• CAS NO: 24347-65-7
• Molecular Formula: C₁₂H₁₃NO₂
• Molecular Weight: 203.2371
• Mol File: 24347-65-7.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 320.4°C at 760 mmHg
• Flash Point: 143.9°C
• Density: 1.14g/cm³
• Vapor Pressure: 0.000319mmHg at 25°C
• Refractive Index: 1.574
• CAS DataBase Reference: (6-nitrocyclohex-3-en-1-yl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (6-nitrocyclohex-3-en-1-yl)benzene(24347-65-7)
• EPA Substance Registry System: (6-nitrocyclohex-3-en-1-yl)benzene(24347-65-7)

Safety Data

• Hazardous Substances Data: 24347-65-7(Hazardous Substances Data)

Usage

Description

(6-nitrocyclohex-3-en-1-yl)benzene, also known as 6-nitrocyclohex-3-en-1-ylbenzene, is an organic compound characterized by its molecular formula C12H11NO2. It is a nitroaromatic compound that features a benzene ring with an attached cyclohexene ring, which has a nitro group (NO2) at the 6-position. This chemical is recognized for its applications in the production of synthetic fragrances and dyes, while also being acknowledged for its potential health and environmental hazards.

Uses

Used in Fragrance Industry:
(6-nitrocyclohex-3-en-1-yl)benzene is used as a key component in the synthesis of various fragrances. Its unique chemical structure contributes to the creation of distinct and appealing scents that are utilized in the perfumery and cosmetic industries.
Used in Dye Industry:
In the dye industry, (6-nitrocyclohex-3-en-1-yl)benzene serves as an essential intermediate for the production of synthetic dyes. Its chemical properties allow for the development of a wide range of colors and hues, which are valuable in various applications such as textiles, plastics, and printing inks.
Used in Chemical Research:
(6-nitrocyclohex-3-en-1-yl)benzene is also utilized in chemical research and development, where it can be further modified or used as a starting material for the synthesis of more complex organic compounds with specific applications in various fields.

Upstream product

• 5153-67-3 nitrostyrene 
• 106-99-0 buta-1,3-diene 
• 77-79-2 3-Sulfolene 

Downstream Products

• 17448-50-9 (+/-)-trans-1-nitro-2-phenyl-cyclohexane 
• 134745-91-8 (+/-)-trans-6-amino-1-phenyl-cyclohexene-⁽³⁾ 
• 134745-92-9 ((1S,6R)-6-Phenyl-cyclohex-3-enyl)-carbamic acid tert-butyl ester 
• 134745-93-0 4-Methyl-N-((1S,6R)-6-phenyl-cyclohex-3-enyl)-benzenesulfonamide 
• 134745-95-2 (1R,5S,8S)-4-Methylene-8-phenyl-2-(toluene-4-sulfonyl)-2-aza-bicyclo[3.3.1]non-6-ene 
• 134745-94-1 N-(2-Bromo-allyl)-4-methyl-N-((1R,6S)-6-phenyl-cyclohex-3-enyl)-benzenesulfonamide 
• 134745-98-5 (1R,5S,8S)-4-Eth-(Z)-ylidene-8-phenyl-2-(toluene-4-sulfonyl)-2-aza-bicyclo[3.3.1]non-6-ene 
• 134745-98-5 (1R,5S,8S)-4-Eth-(E)-ylidene-8-phenyl-2-(toluene-4-sulfonyl)-2-aza-bicyclo[3.3.1]non-6-ene 
• 134745-97-4 N-((E)-2-Iodo-but-2-enyl)-4-methyl-N-((1R,6S)-6-phenyl-cyclohex-3-enyl)-benzenesulfonamide 
• 134745-97-4 N-((Z)-2-Iodo-but-2-enyl)-4-methyl-N-((1R,6S)-6-phenyl-cyclohex-3-enyl)-benzenesulfonamide 
• 5554-79-0 (+/-)-1-aci-1-nitro-2-phenyl-cyclohexane 
• 17448-50-9 cis-1-nitro-2-phenylcyclohexanone 

Relevant articles and documents

Organocatalytic Michael addition/intramolecular Julia-Kocienski olefination for the preparation of nitrocyclohexenes

An asymmetric organocatalytic [3 + 3] annulation strategy based on a Michael addition/intramolecular Julia-Kocienski olefination sequence has been developed for the synthesis of 4-substituted-5-nitrocyclohex-1-ene compounds. The strategy is an alternative to the direct reluctant enantioselective Diels-Alder approach. The potential of the methodology has been demonstrated with a concise enantioselective formal synthesis of trandolapril.