87044-47-1

Basic information

• Product Name: (2,6-dimethyloxan-2-yl)methanol
• Synonyms: (2,6-dimethyloxan-2-yl)methanol
• CAS NO: 87044-47-1
• Molecular Formula: C8H16O2
• Molecular Weight: 144.21144
• Mol File: 87044-47-1.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 193.7°Cat760mmHg
• Flash Point: 65.8°C
• Appearance: /
• Density: 0.933g/cm³
• Vapor Pressure: 0.121mmHg at 25°C
• Refractive Index: 1.433
• CAS DataBase Reference: (2,6-dimethyloxan-2-yl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (2,6-dimethyloxan-2-yl)methanol(87044-47-1)
• EPA Substance Registry System: (2,6-dimethyloxan-2-yl)methanol(87044-47-1)

Safety Data

• Hazardous Substances Data: 87044-47-1(Hazardous Substances Data)

Usage

General Description

(2,6-dimethyloxan-2-yl)methanol, also known as 2,6-dimethyltetrahydropyran-2-ol, is a chemical compound with the molecular formula C7H14O2. It is a colorless liquid with a mild, pleasant odor. (2,6-dimethyloxan-2-yl)methanol is commonly used as a solvent in the production of pharmaceuticals, pesticides, and other chemical compounds. It is also used as a fragrance ingredient and as a flavoring agent in the food industry. Additionally, it has potential applications in the synthesis of organic compounds and serves as an intermediate in the production of various products. While it has various industrial uses, (2,6-dimethyloxan-2-yl)methanol should be handled with care, as it is flammable and may cause skin and eye irritation upon contact.

InChI:InChI=1/C8H16O2/c1-7-4-3-5-8(2,6-9)10-7/h7,9H,3-6H2,1-2H3

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Relevant articles and documents

Ketal-lactone compounds and their stereoselective cleavage to cyclic ethers

The easy preparation of ketal-lactone compounds via Diels-Alder reaction, followed by hydrolysis and cyclization and excellent stereoselective ring opening of the ketal-lactone to 6-membered and 7- membered cyclic ethers are described.

STEREOSELECTIVE REDUCTION OF ACETALS. A METHOD FOR REDUCTIVE GENERATION OF HETEROCYCLIC RING SYSTEMS

A new synthetic process for the construction of oxygen-containing heterocyclic systems starting from bicyclic acetals is described.We have investigated the mechanism and the stereochemical course of the reductive cleavage of acetals.

FACILE PREPARATION OF 2,6-DIMETHYL-2,6-TETRAHYDROPYRANCARBOLACTONE, A VERSATILE INTERMEDIATE FOR THE SYNTHESES OF (+/-)-FRONTALIN, (+/-)-CINENIC ACID, AND (+/-)-LINALOYL OXIDE

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