4292-04-0

Basic information

• Product Name: 1-ISOPROPYL-1-CYCLOHEXENE
• Synonyms: 1-ISOPROPYL-1-CYCLOHEXENE;1-isopropylcyclohexene;1-Isopropylcyclohexene-1;cyclohexene,1-(1-methylethyl)-;1-Isopropy-1-cyclohexene
• CAS NO: 4292-04-0
• Molecular Formula: C₉H₁₆
• Molecular Weight: 124.22
• Product Categories: Acyclic;Alkenes;Organic Building Blocks
• Mol File: 4292-04-0.mol
• Article Data: 9

Chemical Properties

• Melting Point: -91.55°C (estimate)
• Boiling Point: 155-157 °C(lit.)
• Flash Point: 78 °F
• Appearance: /
• Density: 0.824 g/mL at 25 °C(lit.)
• Vapor Pressure: 4.41mmHg at 25°C
• Refractive Index: n20/D 1.455(lit.)
• CAS DataBase Reference: 1-ISOPROPYL-1-CYCLOHEXENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-ISOPROPYL-1-CYCLOHEXENE(4292-04-0)
• EPA Substance Registry System: 1-ISOPROPYL-1-CYCLOHEXENE(4292-04-0)

Safety Data

• Statements: 10
• Safety Statements: 16-29-33
• RIDADR: UN 3295 3/PG 3
• WGK Germany: 3
• HazardClass: 3.2
• PackingGroup: III
• Hazardous Substances Data: 4292-04-0(Hazardous Substances Data)

Usage

Physical state

Colorless liquid

Odor

Faint

Solubility

Insoluble in water, soluble in organic solvents

Uses

Intermediate in the production of other chemicals (pharmaceuticals, agrochemicals), solvent in organic synthesis, fragrance ingredient in perfumes and personal care products

Toxicity

Low

Hazards

Flammable, potential for skin and eye irritation

Safety measures

Handle with care and proper safety measures

InChI:InChI=1/C9H16/c1-8(2)9-6-4-3-5-7-9/h6,8H,3-5,7H2,1-2H3

Upstream product

• 16642-55-0 α,α-dimethyl-1-cyclohexene-1-acetic acid 
• 5749-72-4 isopropylidenecyclohexane 
• 16664-07-6 2-cyclohexyl-2-propanol 
• 3552-01-0 1-isopropyl-cyclohexanol 
• 108-94-1 cyclohexanone 
• 75-26-3 isopropyl bromide 
• 98-82-8 Isopropylbenzene 
• 696-29-7 (1-methylethyl)-cyclohexane 
• 2207-13-8 1-chloro-1-isopropyl-cyclohexane 
• 920-39-8 isopropylmagnesium bromide 
• 90047-74-8 1-Iodo-7-methyl-5,6-octadiene 
• 121694-16-4 3,6-dimethyl-4,5,6,7-tetrahydrobenzothiophene-4-one, dithioethylene ketal 
• 1460-19-1 7,7-dimethylbicyclo[4.1.0]heptane 
• 121694-15-3 3,6-dimethyl-4,5,6,7-tetrahydrobenzothiophene-4-one 

Downstream Products

• 6328-22-9 3-isopropyl-2-cyclohexen-1-one 
• 56335-93-4 (+/-)-1-isopropyl-cyclohexane-1r,2t-diol 
• 5749-72-4 isopropylidenecyclohexane 
• 34969-90-9 2-Isopropyl-3-nitrocyclohexen 
• 69642-10-0 1e-Isopropyl-1a-chloro-2a-nitrosocyclohexan 
• 20937-67-1 6-Acetyl-1-isopropyl-cyclohexen 
• 696-29-7 (1-methylethyl)-cyclohexane 
• 99942-88-8 Acetic acid 3-isopropyl-cyclohex-2-enyl ester 
• 124-04-9 Adipic acid 

Relevant articles and documents

Alternating copolymerization of ethylene with 7-methylenebicyclo[4.1.0] heptane promoted by the cobalt complex. Highly regulated structure and thermal rearrangement of the obtained copolymer

The Co complex-catalyzed copolymerization of ethylene with 7-methylenebicyclo[4.1.0]-heptane was investigated as an alternative copolymer with a highly regulated structure. The thermally induced ring opening reaction of the copolymer, which gives a new po

BF3·OEt2 promotes fast, mild, clean and regioselective dehydration of tertiary alcohols

BF3·OEt2 in methylene chloride at 25°C for 2 hours or less is shown to be effective for easy conversion of tertiary alcohols into the corresponding thermodynamically most stable alkenes.

THIAZOLES IN ORGANIC SYNTHESIS. NOVEL SYNTHESES OF MENTHANES AND EREMOPHILANES

Acetylenic thiazoles of proper design have been shown to undergo an intramolecular Diels-Alder reaction leading to fused-ring thiophene derivatives.When appropriately substituted, these latter materials can be readily converted to terpenes of the menthane