22600-85-7 Usage
Description
(5,5-diMethyltetrahydrofuran-3-yl)Methanol is a chemical compound derived from tetrahydrofuran, a cyclic ether. It is characterized by its low toxicity, high boiling point, and the presence of a hydroxyl group, which makes it suitable for various applications in industrial processes. (5,5-diMethyltetrahydrofuran-3-yl)Methanol is often used as a substitute for traditional solvents like diethyl ether and tetrahydrofuran due to its favorable properties.
Uses
Used in Solvent Applications:
(5,5-diMethyltetrahydrofuran-3-yl)Methanol is used as a solvent in various industrial processes for its low toxicity and high boiling point, making it a safer and more efficient alternative to traditional solvents like diethyl ether and tetrahydrofuran.
Used in Organic Synthesis:
In the field of organic chemistry, (5,5-diMethyltetrahydrofuran-3-yl)Methanol serves as a reagent in numerous chemical reactions, taking advantage of its hydroxyl group and compatibility with a wide range of organic compounds.
Used in Chemical Reactions:
The presence of a hydroxyl group in its structure allows (5,5-diMethyltetrahydrofuran-3-yl)Methanol to be utilized in various chemical reactions, contributing to its popularity in industrial applications.
Safety Precautions:
Check Digit Verification of cas no
The CAS Registry Mumber 22600-85-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,6,0 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22600-85:
(7*2)+(6*2)+(5*6)+(4*0)+(3*0)+(2*8)+(1*5)=77
77 % 10 = 7
So 22600-85-7 is a valid CAS Registry Number.
22600-85-7Relevant articles and documents
A convenient synthesis of 2-alkyl-2-methyltetrahydrofurans from 4- methylalk-4-en-1-ols catalyzed by iodine
Kim, Kyoung Mahn,Jeon, Dong Ju,Ryu, Eung K.
, p. 835 - 836 (1998)
Cyclization of 4-methylalk-4-en-1-ols in the presence of a catalytic amount of iodine in dichloromethane gave exclusively 2-alkyl-2- methyltetrahydrofurans under mild conditions in high yields.
Catalytic Synthesis of Saturated Oxygen Heterocycles by Hydrofunctionalization of Unactivated Olefins: Unprotected and Protected Strategies
Shigehisa, Hiroki,Hayashi, Miki,Ohkawa, Haruna,Suzuki, Tsuyoshi,Okayasu, Hiroki,Mukai, Mayumi,Yamazaki, Ayaka,Kawai, Ryohei,Kikuchi, Harue,Satoh, Yui,Fukuyama, Akane,Hiroya, Kou
supporting information, p. 10597 - 10604 (2016/09/04)
A mild, general, and functional group tolerant intramolecular hydroalkoxylation and hydroacyloxylation of unactivated olefins using a Co(salen) complex, an N-fluoropyridinium salt, and a disiloxane reagent is described. This reaction was carried out at ro
Intramolecular additions of alcohols and carboxylic acids to inert olefins catalyzed by silver(I) triflate
Yang, Cai-Guang,Reich, Nicholas W.,Shi, Zhangjie,He, Chuan
, p. 4553 - 4556 (2007/10/03)
(Chemical Equation Presented) Intramolecular additions of hydroxyl or carboxyl groups to inert olefins catalyzed by simple silver(I) triflate are described. Good to excellent yields can be obtained for a range of substrates under relatively mild conditions. This reaction represents one of the simplest methods to construct cyclic ethers or lactones.
