33426-60-7

Basic information

• Product Name: 1-ISOPROPOXY-2-METHYLBENZENE
• Synonyms: 1-ISOPROPOXY-2-METHYLBENZENE
• CAS NO: 33426-60-7
• Molecular Formula: C₁₀H₁₄O
• Molecular Weight: 150.22
• Mol File: 33426-60-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 198.9°C at 760 mmHg
• Flash Point: 74°C
• Appearance: /
• Density: 0.921g/cm³
• Vapor Pressure: 0.496mmHg at 25°C
• Refractive Index: 1.487
• CAS DataBase Reference: 1-ISOPROPOXY-2-METHYLBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-ISOPROPOXY-2-METHYLBENZENE(33426-60-7)
• EPA Substance Registry System: 1-ISOPROPOXY-2-METHYLBENZENE(33426-60-7)

Safety Data

• Hazardous Substances Data: 33426-60-7(Hazardous Substances Data)

Usage

Physical state

Colorless to pale yellow liquid

Odor

Mild aromatic

Uses

Solvent in industrial applications (e.g. production of paints, coatings, adhesives), found in consumer products (e.g. cleaners, degreasers)

Hazards

Harmful if swallowed or inhaled, may cause skin and eye irritation

Safety measures

Handle with care and take appropriate precautions when working with this chemical.

InChI:InChI=1/C10H14O/c1-8(2)11-10-7-5-4-6-9(10)3/h4-8H,1-3H3

Upstream product

• 95-48-7 ortho-cresol 
• 75-26-3 isopropyl bromide 
• 593-53-3 Methyl fluoride 
• 2741-16-4 isopropoxybenzene 
• 95-46-5 2-methylphenyl bromide 
• 67-63-0 isopropyl alcohol 
• 141-52-6 sodium ethanolate 

Downstream Products

• 1740-97-2 2-methyl-4-isopropylphenol 
• 95-48-7 ortho-cresol 
• 106593-24-2 2-Hydroxy-1-methyl-3.5-diisopropyl-benzol 
• 93308-42-0 isopropyl-(4-isopropyl-2-methyl-phenyl)-ether 
• 60736-78-9 3-chloro-4-(3'-methyl-4'-isopropoxybenzyloxy)-phenylacetic acid 
• 64360-36-7 [4-(4-Isopropoxy-3-methyl-benzyloxy)-phenyl]-acetic acid 
• 69129-66-4 4-Isopropoxy-3-methyl-benzenesulfonyl chloride 
• 60736-72-3 3-methyl-4-iso-propoxybenzyl chloride 

Relevant articles and documents

Streamlined synthesis of the bippyphos family of ligands and cross-coupling applications

We describe the efficient preparation of Bippyphos, 1. The key precursor to Bippyphos, 5, was prepared via a one-pot bromination of diketone 2 followed by alkylation with pyrazole and condensation with phenylhydrazine. Lithiation of 5 and trapping with ditert-butylchlorophosphine afforded Bippyphos, 1. Using this approach we have prepared several derivatives of Bippyphos to probe the structure and activity relationships of this family of phosphine ligands. We also demonstrate the utility of these ligands in Pdcatalyzed amination reactions and other cross-coupling reactions.

Cycloalkanecarboxanilide derivative herbicides

Compounds of the formula STR1 wherein Y is C1-3 alkyl; R1 is an optionally substituted hydrocarbyl group and R2 is alkyl or halogen, are useful as herbicides.

Substituted benzyloxyarylacetic acids: synthesis and quantitative relationships between structure and antiinflammatory activity

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