51200-83-0

Basic information

• Product Name: 2,4-dimethyl-3-(propan-2-yl)pentan-3-ol
• Synonyms: 3-isopropyl-2,4-dimethyl-3-pentanol; 3-Isopropyl-2,4-dimethylpentan-3-ol; 3-Pentanol, 2,4-dimethyl-3- (1-methylethyl)-; 3-pentanol, 2,4-dimethyl-3-(1-methylethyl)-
• CAS NO: 51200-83-0
• Molecular Formula: C₁₀H₂₂O
• Molecular Weight: 158.2811
• Mol File: 51200-83-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 181.3°C at 760 mmHg
• Flash Point: 67.6°C
• Density: 0.823g/cm³
• Vapor Pressure: 0.251mmHg at 25°C
• Refractive Index: 1.43
• CAS DataBase Reference: 2,4-dimethyl-3-(propan-2-yl)pentan-3-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-dimethyl-3-(propan-2-yl)pentan-3-ol(51200-83-0)
• EPA Substance Registry System: 2,4-dimethyl-3-(propan-2-yl)pentan-3-ol(51200-83-0)

Safety Data

• Hazardous Substances Data: 51200-83-0(Hazardous Substances Data)

Usage

General Description

The chemical 2,4-dimethyl-3-(propan-2-yl)pentan-3-ol, also known as diisobutylcarbinol, is an organic compound with the molecular formula C10H22O. It is a colorless liquid with a sweet, floral odor and is commonly used as a solvent and a fragrance ingredient in various products. It is also used as a precursor in the synthesis of other organic compounds. This chemical is flammable and should be handled with care due to its potential hazards.

Upstream product

• 1888-75-1 isopropyllithium 
• 565-80-0 2,4-dimethylpentan-3-one 
• 1068-55-9 isopropylmagnesium chloride 

Downstream Products

• 10412-42-7 2,4-Dimethyl-3-isopropyl-penten-2 
• 74-98-6 propane 
• 565-80-0 2,4-dimethylpentan-3-one 
• 55705-73-2 4-nitro-benzoic acid-(1,1-diisopropyl-2-methyl-propyl ester) 

Relevant articles and documents

LiClO4-Promoted Addition of Alkyl Grignard and Alkynyllithium Reagents to Ketones. Comparison of a 5 M LiClO4/Diethyl Ether Solution with CeCl3

The influence of a 5 M ethereal LiClO4 solution as solvent on the addition of different alkyl Grignard and alkynyllithium reagents to highly enolizable ketones was studied.A comparison with the results in the presence of CeCl3 shows a similar improvement in the yield. - Keywords: Nucleophilic addition; Lewis acid; Enolizable ketones; Alkyl Grignard; Alkynyllithium reagent

CERIUM CHLORIDE-PROMOTED NUCLEOPHILIC ADDITION OF GRIGNARD REAGENTS TO KETONES AN EFFICIENT METHOD FOR THE SYNTHESIS OF TERTIARY ALCOHOLS

In the presence of anhydrous cerium(III) chloride, Grignard reagents react with ketones to afford addition products in high yields, even though the substrates are susceptible to abnormal reactions with Grignard reagents alone.