1123786-92-4 Usage
Description
[(3S)-3-Methyloxolan-3-yl]Methanol is a chiral alcohol with the molecular formula C6H12O2, featuring a six-membered ring with an oxygen atom and a methyl group attached to it. This versatile chemical is widely used in various industrial and research applications.
Uses
Used in Organic Synthesis:
[(3S)-3-Methyloxolan-3-yl]Methanol is used as a building block in organic synthesis for the preparation of various pharmaceuticals and agrochemicals. Its unique structure and properties make it a valuable component in the creation of complex organic molecules.
Used in Pharmaceutical Industry:
[(3S)-3-Methyloxolan-3-yl]Methanol is used as an intermediate in the production of pharmaceuticals, contributing to the development of new drugs and medicines.
Used in Agrochemical Industry:
[(3S)-3-Methyloxolan-3-yl]Methanol is used as a precursor in the synthesis of agrochemicals, aiding in the development of effective crop protection products.
Used as a Solvent:
[(3S)-3-Methyloxolan-3-yl]Methanol is used as a solvent in some chemical reactions, facilitating the process and improving the efficiency of certain chemical processes.
Used in Fragrance and Flavor Production:
[(3S)-3-Methyloxolan-3-yl]Methanol has potential applications in the production of fragrances and flavors due to its unique structure and properties, offering a distinct scent and taste profile for various consumer products.
Check Digit Verification of cas no
The CAS Registry Mumber 1123786-92-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,3,7,8 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1123786-92:
(9*1)+(8*1)+(7*2)+(6*3)+(5*7)+(4*8)+(3*6)+(2*9)+(1*2)=154
154 % 10 = 4
So 1123786-92-4 is a valid CAS Registry Number.
1123786-92-4Relevant articles and documents
A broadly applicable and practical oligomeric (salen)Co catalyst for enantioselective epoxide ring-opening reactions
White, David E.,Tadross, Pamela M.,Lu, Zhe,Jacobsen, Eric N.
, p. 4165 - 4180 (2014/06/09)
The (salen)Co catalyst (4a) can be prepared as a mixture of cyclic oligomers in a short, chromatography-free synthesis from inexpensive, commercially available precursors. This catalyst displays remarkable enhancements in reactivity and enantioselectivity relative to monomeric and other multimeric (salen)Co catalysts in a wide variety of enantioselective epoxide ring-opening reactions. The application of catalyst 4a is illustrated in the kinetic resolution of terminal epoxides by nucleophilic ring-opening with water, phenols, and primary alcohols; the desymmetrization of meso epoxides by addition of water and carbamates; and the desymmetrization of oxetanes by intramolecular ring opening with alcohols and phenols. The favorable solubility properties of complex 4a under the catalytic conditions facilitated mechanistic studies, allowing elucidation of the basis for the beneficial effect of oligomerization. Finally, a catalyst selection guide is provided to delineate the specific advantages of oligomeric catalyst 4a relative to (salen)Co monomer 1 for each reaction class.
