21315-20-8

Basic information

• Product Name: 2-(2-Methylpropyloxy)phenol
• Synonyms: 2-(2-Methylpropyloxy)phenol;2-isobutoxyphenol(SALTDATA: FREE);2-isobutoxyphenol
• CAS NO: 21315-20-8
• Molecular Formula: C₁₀H₁₄O₂
• Molecular Weight: 166.22
• Mol File: 21315-20-8.mol
• Article Data: 4

Chemical Properties

• Melting Point: 50-51 °C
• Boiling Point: 248.4°C at 760 mmHg
• Flash Point: 95.3°C
• Appearance: /
• Density: 1.027g/cm³
• Vapor Pressure: 0.0154mmHg at 25°C
• Refractive Index: 1.513
• PKA: 9?+-.0.30(Predicted)
• CAS DataBase Reference: 2-(2-Methylpropyloxy)phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-Methylpropyloxy)phenol(21315-20-8)
• EPA Substance Registry System: 2-(2-Methylpropyloxy)phenol(21315-20-8)

Safety Data

• Hazardous Substances Data: 21315-20-8(Hazardous Substances Data)

Usage

Appearance

Pale yellow oily liquid

Odor

Smoky, phenolic

Common uses

Production of pharmaceuticals, perfume industry

Building block

Synthesis of various organic compounds

Properties

Antimicrobial, antioxidant, anti-inflammatory

Ingredient in

Medical and cosmetic products formulation

Flavoring agent

Used in food industry

Natural occurrence

Found in some plant oils

Industrial and commercial applications

Wide range due to versatile properties

InChI:InChI=1/C10H14O2/c1-8(2)7-12-10-6-4-3-5-9(10)11/h3-6,8,11H,7H2,1-2H3

Upstream product

• 81995-32-6 2-(i-butoxy)benzaldehyde 
• 90-02-8 salicylaldehyde 
• 513-38-2 Isobutyl iodide 
• 120-80-9 benzene-1,2-diol 
• 21645-25-0 phenol 2-[(tetrahydro-2H-pyran-2yl)oxy] 

Downstream Products

• 1091600-28-0 C₂₆H₂₇Cl₂NO₅ 
• 1396943-10-4 1-hexyloxy-2-isobutoxybenzene 
• 1396943-12-6 1-decyloxy-2-isobutoxybenzene 
• 1396943-17-1 1-decyloxy-2-isobutoxy-4,5-dinitrobenzene 
• 1396943-18-2 1-dodecyloxy-2-isobutoxy-4,5-dinitrobenzene 
• 1396943-29-5 3,11-dibutoxy-2,12-diisobutoxy-7,16-bis(2-hydroxybenzoyl)-5,14-dihydrodibenzo[b,i][1,4,8,11]tetraazacyclotetradecine 
• 1396943-24-0 3,12-dibutoxy-2,11-diisobutoxy-7,16-bis(2-hydroxybenzoyl)-5,14-dihydrodibenzo[b,i][1,4,8,11]tetraazacyclotetradecine 
• 1396943-30-8 3,11-dihexyloxy-2,12-diisobutoxy-7,16-bis(2-hydroxybenzoyl)-5,14-dihydrodibenzo[b,i][1,4,8,11]tetraazacyclotetradecine 
• 1396943-25-1 3,12-dihexyloxy-2,11-diisobutoxy-7,16-bis(2-hydroxybenzoyl)-5,14-dihydrodibenzo[b,i][1,4,8,11]tetraazacyclotetradecine 
• 1396943-31-9 2,12-diisobutoxy-3,11-dioctoxy-7,16-bis(2-hydroxybenzoyl)-5,14-dihydrodibenzo[b,i][1,4,8,11]tetraazacyclotetradecine 
• 1396943-26-2 2,11-diisobutoxy-3,12-dioctoxy-7,16-bis(2-hydroxybenzoyl)-5,14-dihydrodibenzo[b,i][1,4,8,11]tetraazacyclotetradecine 
• 1396943-32-0 3,11-didecyloxy-2,12-diisobutoxy-7,16-bis(2-hydroxybenzoyl)-5,14-dihydrodibenzo[b,i][1,4,8,11]tetraazacyclotetradecine 
• 1396943-27-3 3,12-didecyloxy-2,11-diisobutoxy-7,16-bis(2-hydroxybenzoyl)-5,14-dihydrodibenzo[b,i][1,4,8,11]tetraazacyclotetradecine 
• 1396943-33-1 3,11-didodecyloxy-2,12-diisobutoxy-7,16-bis(2-hydroxybenzoyl)-5,14-dihydrodibenzo[b,i][1,4,8,11]tetraazacyclotetradecine 

Relevant articles and documents

Tuning the mesomorphic properties of liquid-crystalline dibenzotetraaza[14]annulenes - Discotic nematic phases of tetraalkoxy- substituted derivatives

A homologous series of five tetrasubstituted dibenzotetraaza[14]annulene- based discotic mesogens was prepared and studied using polarizing optical microscopy (POM) and differential scanning calorimetry (DSC). A nematic phase was identified for the product bearing two peripheral isobutoxy and two dodecyloxy substituents.

INSECTICIDAL CARBAMATES EXHIBITING SPECIES-SELECTIVE INHIBITION OF ACETYLCHOLINESTERASE (AChE)

The present invention includes insecticidal carbamates that are useful, for example, for the control of insects, such as mosquitoes, which can be used in applications where exposure to and/or contact with humans is likely. The insecticides of the present invention include phenyl N-methyl carbamates and compositions comprising them that exhibit species-selective inhibition of acetylcholinesterase (AChE) and are preferably toxic to mosquitoes but not humans. Of particular interest are compounds of Formula (I) and Formula (II): Compounds of Formula (I) and Formula (II) are especially suitable for insecticide treated nets and indoor residual spraying for mosquito control.