61266-55-5

Basic information

• Product Name: (4,4-DiMethyloxetan-2-yl)Methanol
• Synonyms: (4,4-DiMethyloxetan-2-yl)Methanol
• CAS NO: 61266-55-5
• Molecular Formula: C₆H₁₂O₂
• Molecular Weight: 116.15828
• Mol File: 61266-55-5.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: Inert atmosphere,Store in freezer, under -20°C
• CAS DataBase Reference: (4,4-DiMethyloxetan-2-yl)Methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (4,4-DiMethyloxetan-2-yl)Methanol(61266-55-5)
• EPA Substance Registry System: (4,4-DiMethyloxetan-2-yl)Methanol(61266-55-5)

Safety Data

• Hazardous Substances Data: 61266-55-5(Hazardous Substances Data)

Usage

General Description

(4,4-DiMethyloxetan-2-yl)Methanol is a chemical compound with the molecular formula C7H14O2. It is a colorless liquid with a faint, pleasant odor. (4,4-DiMethyloxetan-2-yl)Methanol is used in various industrial applications, including as a solvent and as a raw material for the production of other chemicals. It is also used in the pharmaceutical industry as an intermediate for the synthesis of various drugs. Additionally, (4,4-DiMethyloxetan-2-yl)Methanol is used in the manufacture of flavors and fragrances. However, it is important to handle this compound with care, as it can be harmful if it comes into contact with the skin or if it is inhaled. Overall, (4,4-DiMethyloxetan-2-yl)Methanol is a versatile chemical with a range of industrial and pharmaceutical applications.

Upstream product

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Downstream Products

• 119205-26-4 4-Benzenesulfonylmethyl-2,2-dimethyl-oxetane 
• 122220-07-9 (E)-5-Benzenesulfonyl-2-methyl-pent-4-en-2-ol 

Relevant articles and documents

Preparation method and application of 2-hydroxymethyloxetane derivative

The invention discloses a preparation method and application of a 2-hydroxymethyloxetane derivative. The method comprises the following steps that a compound II and a compound III are used as raw materials; Barbier reaction is performed to obtain a compound IV; olefinic bonds in the compound IV are cyclized and oxidized to obtain a compound V; under the alkaline condition, ring opening is performed to generate a compound VI; after ring closing reaction, a compound VII is obtained; finally, benzyl protecting groups are removed to obtain the 2-hydroxymethyloxetane derivative (the compound I).

CONCERTED VERSUS STEPWISE PROCESSES IN ELIMINATIVE FISSION OF OXACYCLES

2-Phenylsulphonylmethyloxetan (2a) has been synthesised and the kinetics of base-promoted eliminative ring fission have been determined.The results show, by comparison with the behaviour of related substrates studied previously, that (i) the 3-ring,:4-rin

TRANSPOSITION DES OXIRANNES-ETHANOLS PAR L'INTERMEDIAIRE D'ALCOXYETAINS. INFLUENCE DE LA CONFIGURATION DE L'OXIRANNE

The transposition of oxirane-ethanols, through alkoxytin compounds, into oxetane-2-methanols and/or oxolan-3-ols (tetrahydrofuran-3-ols) is dependent upon the oxirane configuration.Cis configuration is more suitable for the formation of the smallest ring.Steric hindrance is not sufficient enough to explain the results.