1123-26-8 Usage
Description
1-(1-hydroxyethyl)cyclohexanol, with the molecular formula C8H16O2, is a cyclic alcohol featuring a hydroxyethyl group attached to the cyclohexane ring. It is recognized for its mild, pleasant odor and its capacity to dissolve a broad spectrum of substances, making it a versatile compound with a range of applications across different industries.
Uses
Used in Fragrance and Flavor Industry:
1-(1-hydroxyethyl)cyclohexanol is used as a key component for creating fragrances and flavors due to its mild, pleasant odor, enhancing the sensory experience of various products.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 1-(1-hydroxyethyl)cyclohexanol serves as a vital intermediate in the synthesis of other organic compounds, contributing to the development of new medications and therapies.
Used as a Solvent:
1-(1-hydroxyethyl)cyclohexanol is utilized as a solvent in various industrial applications, capitalizing on its ability to dissolve a wide range of substances, which facilitates numerous chemical processes and reactions.
Overall, 1-(1-hydroxyethyl)cyclohexanol is a chemical compound with diverse applications, valued for its unique properties and versatility in different sectors, including the fragrance and flavor industry, pharmaceuticals, and as a solvent in industrial processes.
Check Digit Verification of cas no
The CAS Registry Mumber 1123-26-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1123-26:
(6*1)+(5*1)+(4*2)+(3*3)+(2*2)+(1*6)=38
38 % 10 = 8
So 1123-26-8 is a valid CAS Registry Number.
1123-26-8Relevant articles and documents
Catalytic Reductive Pinacol-Type Rearrangement of Unactivated 1,2-Diols through a Concerted, Stereoinvertive Mechanism
Drosos, Nikolaos,Cheng, Gui-Juan,Ozkal, Erhan,Cacherat, Bastien,Thiel, Walter,Morandi, Bill
supporting information, p. 13377 - 13381 (2017/10/17)
A catalytic pinacol-type reductive rearrangement reaction of internal 1,2-diols is reported herein. Several scaffolds not usually amenable to pinacol-type reactions, such as aliphatic secondary–secondary diols, undergo the transformation well without the need for prefunctionalization. The reaction uses a simple boron catalyst and two silanes and proceeds through a concerted, stereoinvertive mechanism that enables the preparation of highly enantiomerically enriched products. Computational studies have been used to rationalize the preference for migration over direct deoxygenation.
Alkene syn dihydroxylation with malonoyl peroxides
Griffith, James C.,Jones, Kevin M.,Picon, Sylvain,Rawling, Michael J.,Kariuki, Benson M.,Campbell, Matthew,Tomkinson, Nicholas C. O.
supporting information; experimental part, p. 14409 - 14411 (2010/12/24)
Cyclopropyl malonoyl peroxide (1), which can be prepared in a single step from the commercially available diacid, is an effective reagent for the dihydroxylation of alkenes. Reaction of 1 with an alkene in the presence of 1 equiv of water at 40 °C followed by alkaline hydrolysis leads to the corresponding diol (40-93%). With 1,2-disubstituted alkenes, the reaction proceeds with syn selectivity (3:1 to >50:1). A mechanism consistent with the experimental findings that is supported by oxygen-labeling studies is proposed.
