19550-30-2

Basic information

• Product Name: 2,3-dimethylbutan-1-ol
• Synonyms: 2,3-dimethylbutan-1-ol
• CAS NO: 19550-30-2
• Molecular Formula: C₆H₁₄O
• Molecular Weight: 102.17476
• EINECS: 243-153-0
• Mol File: 19550-30-2.mol
• Article Data: 29

Chemical Properties

• Melting Point: -48.42°C (estimate)
• Boiling Point: 141.85°C
• Flash Point: 38.6°C
• Appearance: /
• Density: 0.8255
• Vapor Pressure: 2.32mmHg at 25°C
• Refractive Index: 1.4185
• PKA: 15.01±0.10(Predicted)
• CAS DataBase Reference: 2,3-dimethylbutan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-dimethylbutan-1-ol(19550-30-2)
• EPA Substance Registry System: 2,3-dimethylbutan-1-ol(19550-30-2)

Safety Data

• Hazardous Substances Data: 19550-30-2(Hazardous Substances Data)

Usage

General Description

2,3-dimethylbutan-1-ol is a chemical compound with the molecular formula C6H14O. It is a colorless liquid with a mild, sweet odor, and it is soluble in water and ethanol. 2,3-dimethylbutan-1-ol is mainly used as a solvent in various industrial processes, such as paint, ink, and resin production. It is also employed as a flavoring agent in the food industry and as a fragrance ingredient in perfumes and personal care products. Additionally, 2,3-dimethylbutan-1-ol can be utilized in the synthesis of other organic compounds, and it may have potential applications in pharmaceuticals and medicine. However, it is important to handle this chemical with care, as it can cause skin and eye irritation and may be harmful if ingested or inhaled in large quantities.

InChI:InChI=1/C6H14O/c1-5(2)6(3)4-7/h5-7H,4H2,1-3H3

Upstream product

• 83-27-2 sec-butyl-malonic acid diethyl ester 
• 14287-61-7 2,3-dimethylbutyric acid 
• 51760-90-8 2,3-dimethylbutyryl chloride 
• 30540-29-5 butanoic acid, 2,3-dimethyl-, methyl ester 
• 563-79-1 2,3-Dimethyl-2-butene 
• 563-78-0 2,3-Dimethyl-1-butene 
• 79-29-8 2,3-dimethylbutane 
• 54004-42-1 2,3-dimethyl-butanoic acid, ethyl ester 
• 24310-68-7 1,1,2-trimethylpropyldioxy 
• 102925-89-3 2,3-dimethylbutyldioxy 
• 108-64-5 Ethyl isovalerate 
• 201230-82-2 carbon monoxide 
• 78-79-5 isoprene 
• 15019-26-8 (R)-2,3-dimethyl-butyric acid methyl ester 

Downstream Products

• 71412-26-5 acetic acid-(2,3-dimethyl-butyl ester) 
• 55504-67-1 (2,3-Dimethyl-butoxysulfonyl)-phenyl-acetic acid 
• 600-06-6 1-chloro-2,3-dimethylbutane 
• 111042-72-9 (2S)-2,3-dimethylbutyl (S)-3,3,3-trifluoro-2-methoxy-2-phenylpropionate 
• 1900-53-4 24-methylcholest-5-en-3β-yl acetate 
• 1900-53-4 campesteryl acetate 
• 2638-57-5 brassicasterol 
• 68702-73-8 (R)-(-)-(2,3-dimethylbutyl)triphenylphosphonium iodide 
• 152912-17-9 (R)-2,3-dimethylbutyl 4-methylbenzenesulfonate 
• 91638-67-4 (2,3-dimethylbutyl)(phenyl)sulfane 
• 49642-48-0 2,3-dimethylbutanal 
• 4417-80-5 3-methyl-2-methylene-butyraldehyde 
• 15139-34-1 Toluene-4-sulfonic acid (S)-1-[(S)-1-((3S,8S,9S,10R,13S,14S,17R)-3-methoxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-ethyl]-3,4-dimethyl-pentyl ester 
• 68702-73-8 rac-(2,3-Dimethylbutyl)triphenylphosphonium iodide 

Relevant articles and documents

A novel chemiluminescence from the reaction of dioxiranes with alkanes. Proposed mechanism of oxygen-transfer chemiluminescence

Oxidation of adamantane and 2,3-dimethylbutane by methyl(trifluoromethyl)dioxirane is accompanied by chemiluminescence (CL); formation of the emitter of CL, triplet excited trifluoropropanone, is proposed to occur via a concerted oxenoid mechanism of oxygen insertion into C-H bond of the hydrocarbons.

-

-

Ligand-Controlled Direct Hydroformylation of Trisubstituted Olefins

The direct hydroformylation of trisubstituted olefins has been achieved with a combination of a Rh(I) catalyst and a π-acceptor phosphorus (briphos) ligand. A sterically bulky briphos ligand with a large cone angle that forms a 1:1 complex with Rh(I) is found to be reactive for the hydroformylation of trisubstituted olefins. The aldehyde products were obtained with high diastereoselectivity (>99:1) and regioselectivity (49%-81%).

Copper-catalyzed enantioselective hydroboration of unactivated 1, 1-disubstituted alkenes

We report an efficient and highly enantioselective hydroboration of aliphatic 1, 1-disubstituted alkenes with pinacolborane using a phosphine-Cu catalyst. The method allows facile preparation of enantiomerically enriched β-chiral alkyl pinacolboronates from a range of 1, 1-disubstituted alkenes with high enantioselectivity up to 99% ee. Unprecedented enantiodiscrimination between the geminal alkyl substituents was observed with functional group compatibility in the hydroboration. Furthermore, a catalyst loading as low as 1 mol % furnished the desired product without a decrease in yield or selectivity, demonstrating its efficiency in gram scale synthesis.