38393-92-9

Basic information

• Product Name: 3,3-DIMETHYL-1-INDANOL
• Synonyms: 3,3-DIMETHYL-1-INDANOL;1,1-Dimethylindan-3-ol;3,3-Dimethyl-2,3-dihydro-1H-inden-1-ol;3,3-Dimethylindan-1-ol;1-Indanol, 3,3-dimethyl-
• CAS NO: 38393-92-9
• Molecular Formula: C₁₁H₁₄O
• Molecular Weight: 162.23
• Mol File: 38393-92-9.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 264.1°Cat760mmHg
• Flash Point: 100.3°C
• Appearance: /
• Density: 1.053g/cm³
• Vapor Pressure: 0.00498mmHg at 25°C
• Refractive Index: 1.554
• PKA: 14.26±0.40(Predicted)
• CAS DataBase Reference: 3,3-DIMETHYL-1-INDANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3-DIMETHYL-1-INDANOL(38393-92-9)
• EPA Substance Registry System: 3,3-DIMETHYL-1-INDANOL(38393-92-9)

Safety Data

• Hazardous Substances Data: 38393-92-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H14O/c1-11(2)7-10(12)8-5-3-4-6-9(8)11/h3-6,10,12H,7H2,1-2H3

Upstream product

• 26465-81-6 3,3-dimethylindan-1-one 
• 6630-33-7 ortho-bromobenzaldehyde 
• 1010-48-6 3-methyl-3-phenylbutanoic acid 
• 541-47-9 3-Methylbutenoic acid 
• 71-43-2 benzene 

Downstream Products

• 18636-55-0 1,1-dimethyl-1H-indene 
• 1202577-59-0 Methyl (3S)-3-{4-[(3,3-dimethyl-2,3-dihydro-1H-inden-1-yl)oxy]phenyl}-3-ethoxypropionate 
• 1499076-71-9 N-((1,1-dimethyl-1H-inden-2-yl)methyl)-4-methyl-N-phenylbenzenesulfonamide 
• 1499076-73-1 N-((1,1-dimethyl-1H-inden-2-yl)methyl)-N-phenylmethanesulfonamide 
• 1499077-04-1 N-((1,1-dimethyl-1H-inden-2-yl)methyl)-4-isopropylaniline 
• 1499076-07-1 6a-fluoro-7,7-dimethyl-5-tosyl-6,6a,7,11b-tetrahydro-5H-indeno[2,1-c]quinoline 
• 1499076-09-3 2-chloro-6a-fluoro-7,7-dimethyl-5-tosyl-6,6a,7,11b-tetrahydro-5H-indeno[2,1-c]quinoline 
• 1499076-10-6 6a-fluoro-2-isopropyl-7,7-dimethyl-5-((4-nitrophenyl)sulfonyl)-6,6a,7,11b-tetrahydro-5H-indeno[2,1-c]quinoline 
• 1499076-75-3 N-((1,1-dimethyl-1H-inden-2-yl)methyl)-N-(4-isopropylphenyl)-4-methylbenzenesulfonamide 
• 1499076-12-8 2-chloro-5-((4-chlorophenyl)sulfonyl)-6a-fluoro-7,7-dimethyl-6,6a,7,11b-tetrahydro-5H-indeno[2,1-c]quinoline 
• 1499077-05-2 4-chloro-N-((1,1-dimethyl-1H-inden-2-yl)methyl)aniline 
• 1499076-77-5 N-(4-chlorophenyl)-N-((1,1-dimethyl-1H-inden-2-yl)methyl)-4-methylbenzenesulfonamide 
• 1499076-79-7 N-((1,1-dimethyl-1H-inden-2-yl)methyl)-N-(4-isopropylphenyl)-4-nitrobenzenesulfonamide 
• 1499076-88-8 4-chloro-N-(4-chlorophenyl)-N-((1,1-dimethyl-1H-inden-2-yl)methyl)benzenesulfonamide 

Relevant articles and documents

Bench-Stable Nickel Precatalysts with Heck-type Activation

Herein, we report the synthesis and characterization of a new class of air- and moisture-stable phosphine-containing nickel(II) precatalysts, which activate through a Heck-type mechanism. The activities of the precatalysts are demonstrated with a carbonyl

Sodium Bromide-Catalyzed Oxidation of Secondary Benzylic Alcohols Using Aqueous Hydrogen Peroxide as Terminal Oxidant

A halide salt, hydroperoxide and AcOH catalyst system was applied to the oxidation of secondary benzylic alcohols. This simple system can be applied to a variety of secondary benzylic alcohols and scaled up for gram-scale preparation. High secondary benzylic alcohol selectivity of the present method is demonstrated in hydroxyketone synthesis. Based on several experimental results, a catalytic cycle for our oxidation is proposed.

Asymmetric electrophilic fluorocyclization with carbon nucleophiles

Twist of 'F'ate: Various helical-shaped fluorinated tetracyclic molecules were prepared by fluorocarbocyclization of prochiral alkenes. The development of a new class of chiral Selectfluor (1) proved instrumental in developing an asymmetric variant of this transformation. These novel chiral N-F reagents are readily accessible by fluorine transfer from shelf-stable N-fluoropyridinium salts. Copyright