75658-83-2 Usage
Description
Cyclopentane-1,2-diyldimethanol is a chemical compound with the molecular formula C7H14O2. It is a colorless liquid that is used in various industrial applications, including as a solvent and in the production of other chemicals. It is a bifunctional molecule, meaning it contains two hydroxyl (OH) groups, which makes it useful for creating polymers and resins.
Uses
Used in Chemical Industry:
Cyclopentane-1,2-diyldimethanol is used as a solvent for various chemical reactions due to its ability to dissolve a wide range of substances.
Used in Polymer and Resin Production:
Cyclopentane-1,2-diyldimethanol is used as a monomer or building block for creating polymers and resins because of its two hydroxyl (OH) groups.
Used in Pharmaceutical Synthesis:
Cyclopentane-1,2-diyldimethanol is used as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs.
Used in Agrochemical Production:
Cyclopentane-1,2-diyldimethanol is used in the synthesis of agrochemicals, such as pesticides and herbicides, to improve agricultural productivity.
Used in Adhesives, Coatings, and Sealants:
Cyclopentane-1,2-diyldimethanol is used as a component in the production of adhesives, coatings, and sealants, enhancing their performance and durability.
Check Digit Verification of cas no
The CAS Registry Mumber 75658-83-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,6,5 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 75658-83:
(7*7)+(6*5)+(5*6)+(4*5)+(3*8)+(2*8)+(1*3)=172
172 % 10 = 2
So 75658-83-2 is a valid CAS Registry Number.
75658-83-2Relevant articles and documents
Enantiotopic-Place Selective C-H Oxidation Using a (Salen)manganese(III) Complex as a Catalyst
Miyafuji, Akio,Katsuki, Tsutomu
, p. 836 - 838 (1997)
A highly enantiotopic-place selective C-H oxidation of cyclic ether (up to 82% ee) was first achieved by using (R,R)-(salen)manganese(III) complex 8 as a catalyst.
Williamson Ether Synthesis with Phenols at a Tertiary Stereogenic Carbon: Formal Enantioselective Phenoxylation of β-Keto Esters
Shibatomi, Kazutaka,Kotozaki, Manato,Sasaki, Nozomi,Fujisawa, Ikuhide,Iwasa, Seiji
supporting information, p. 14095 - 14098 (2015/09/28)
The enantioselective formation of α-aryloxy-β-keto esters is described for the first time. Lewis acid catalyzed enantioselective chlorination of β-keto esters and subsequent SN2 reactions with phenols yielded α-aryloxy-β-keto esters with up to 96 % ee. Favorskii rearrangement of α-chloro-β-keto esters was also found to give 1,2-diesters with slightly reduced enantiopurity.
An efficient oxidative lactonization of 1,4-diols catalyzed by Cp*Ru(PN) complexes
Ito, Masato,Osaku, Akihide,Shiibashi, Akira,Ikariya, Takao
, p. 1821 - 1824 (2008/02/02)
An efficient oxidative lactonization of 1,4-diols in acetone is accomplished by the well-defined ruthenium catalyst, whose bifunctional nature underlies the high efficiency as well as unique chemo- and regioselectivity of the reaction which provides a rapid access to γ-butyrolactones including flavor lactones hinokinin, and muricatacin.