3710-23-4

Basic information

• Product Name: 2-ISOPROPENYLNAPHTHALENE
• Synonyms: 2-ISOPROPENYLNAPHTHALENE;2-(1-methylvinyl)naphthalene;1-(2-Naphthyl)-1-methylethene;2-(1-Methylethenyl)naphthalene;2-(2-Naphthyl)-1-propene;2-(2-Naphthyl)propene
• CAS NO: 3710-23-4
• Molecular Formula: C₁₃H₁₂
• Molecular Weight: 168.23
• EINECS: 223-053-3
• Mol File: 3710-23-4.mol
• Article Data: 67

Chemical Properties

• Melting Point: 55 °C
• Boiling Point: 155 °C / 11mmHg
• Flash Point: 123.5°C
• Appearance: /
• Density: 0.993g/cm³
• Vapor Pressure: 0.00617mmHg at 25°C
• Refractive Index: 1.604
• CAS DataBase Reference: 2-ISOPROPENYLNAPHTHALENE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-ISOPROPENYLNAPHTHALENE(3710-23-4)
• EPA Substance Registry System: 2-ISOPROPENYLNAPHTHALENE(3710-23-4)

Safety Data

• Hazard Codes: N
• Statements: 50/53
• Safety Statements: 60-61
• Hazardous Substances Data: 3710-23-4(Hazardous Substances Data)

Usage

General Description

2-Isopropylnaphthalene, also known as beta-isopropylnaphthalene, is a chemical compound with the molecular formula C12H12. It is a colorless liquid with a faint odor and is primarily used as a fragrance ingredient in various consumer products such as soaps, detergents, and cosmetics. It is also used as a solvent in chemical processes and as a synthetic intermediate in the production of other chemicals. 2-Isopropylnaphthalene is considered to have low toxicity, and there is limited information available about its potential health effects or environmental impact. However, as with all chemicals, proper safety precautions should be followed when handling and using this substance.

InChI:InChI=1/C13H12/c1-10(2)12-8-7-11-5-3-4-6-13(11)9-12/h3-9H,1H2,2H3

Upstream product

• 917-64-6 methyl magnesium iodide 
• 3007-91-8 ethyl-2-naphthoate 
• 93-08-3 methyl 2-naphthyl ketone 
• 67-71-0 dimethylsulfone 
• 1592-38-7 2-Naphthalenemethanol 
• 7228-47-9 2-(2-naphthyl)ethanol 
• 128155-59-9 2-(2-Naphthyl)-2-thiomethoxy-1,3-dithiane 
• 20351-54-6 2-(2-hydroxy-2-methylethyl)naphthalene 
• 37827-83-1 naphthalene-2-carbonyl fluoride 
• 75-24-1 trimethylaluminum 
• 2243-83-6 2-naphthaloyl chloride 
• 75-16-1 methylmagnesium bromide 
• 941-98-0 1'-naphthacetophenone 
• 1779-49-3 Methyltriphenylphosphonium bromide 

Downstream Products

• 1254470-62-6 4-methyl-N-(2-(naphthalen-2-yl)allyl)benzenesulfonamide 
• 1420904-72-8 C₂₁H₁₉NO₃ 
• 1308661-36-0 2-(naphthalen-2-yl)-1-tosylpropan-2-ol 

Related news

Synthesis of a water-soluble block copolymer of 2-ISOPROPENYLNAPHTHALENE (cas 3710-23-4) and methacrylic acid bearing a pyrene group107/17/2019

An anionic method for preparation of water-soluble block copolymer of 2-isopropenylnaphthalene and methacrylic acid poly(2-IPN-b-MAA), containing pyrene group as a terminal probe, is described. The polymerization process was carried out by an indirect method employing trimethylsilyl methacrylate...detailed

Anionic polymerization and polymer properties of 2-ISOPROPENYLNAPHTHALENE (cas 3710-23-4) and 2-vinylnaphthalene07/14/2019

2-Isopropenylnaphthalene (2-IPN) and 2-vinylnaphthalene (2-VN) were polymerized in toluene with sec-butyllithium initiator. For 2-IPN, equilibrium monomer concentrations were determined, as well as the enthalpy, entropy and ‘absolute’ ceiling temperature, for its polymerization. Densities of b...detailed

Relevant articles and documents

METHOD FOR OXIDATIVE CLEAVAGE OF COMPOUNDS WITH UNSATURATED DOUBLE BOND

A method for oxidative cleavage of a compound with an unsaturated double bond is provided. The method includes the steps of: (A) providing a compound (I) with an unsaturated double bond, a trifluoromethyl-containing reagent, and a catalyst; wherein, the catalyst is represented by Formula (II): M(O)mL1yL2z??(II);wherein, M, L1, L2, m, y, z, R1, R2 and R3 are defined in the specification; and(B) mixing the compound with an unsaturated double bond and the trifluoromethyl-containing reagent to perform an oxidative cleavage of the compound with the unsaturated double bond by using the catalyst in air or under oxygen atmosphere condition to obtain a compound represented by Formula (III):

METHOD FOR OXIDATIVE CLEAVAGE OF COMPOUNDS WITH UNSATURATED DOUBLE BOND

A method for oxidative cleavage of a compound with an unsaturated double bond is provided. The method comprises the following step: (A) providing a compound (I) with an unsaturated double bond, a reagent with trifluoromethyl, and a catalyst; wherein the catalyst is represented by the following formula (II): M(O)mL1yL2z (II); wherein, M, L1, L2, m, y, z, R1, R2 and R3 are defined in the specification; and (B) mixing the compound with an unsaturated double bond and the reagent with a trifluoromethyl to perform an oxidation of the compound with the unsaturated double bond by using the catalyst at air or an oxygen condition to get a compound presented as formula (III):

Visible-Light-Induced Meerwein Fluoroarylation of Styrenes

An unprecedented approach for assembling a broad range of 1,2-diarylethane derivatives with fluorine-containing fully substituted carbon centers was developed. The protocol features straightforward operation, proceeds under metal-free condition, and accommodates a large variety of synthetically useful functionalities. The critical aspect to the success of this novel transformation lies in using aryldiazonium salts as both aryl radical progenitor and also as single electron acceptor which elegantly enables a radical-polar crossover manifold.