52437-39-5 Usage
Description
(R)-2,2,3-trimethylcyclopent-3-ene-1-ethanol, a colorless liquid with a molecular formula of C10H18O, is a derivative of cyclopentene featuring a chiral center that results in the R stereochemistry designation. (R)-2,2,3-trimethylcyclopent-3-ene-1-ethanol is characterized by its pleasant odor and volatility, making it a valuable component in various industries.
Uses
Used in Fragrance Industry:
(R)-2,2,3-trimethylcyclopent-3-ene-1-ethanol is used as a fragrance ingredient in the perfume and personal care products industry due to its pleasant odor and ability to contribute to the overall olfactory profile of a product.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (R)-2,2,3-trimethylcyclopent-3-ene-1-ethanol is used as a potential building block for the development of new drugs, leveraging its unique chemical structure and properties.
Used in Organic Synthesis:
(R)-2,2,3-trimethylcyclopent-3-ene-1-ethanol is utilized as a building block in organic synthesis, where its chiral center and cyclopentene structure can be exploited to create a variety of complex organic compounds for different applications.
Used in Industrial Applications:
As a chemical intermediate, (R)-2,2,3-trimethylcyclopent-3-ene-1-ethanol may have potential industrial applications, particularly in the development of new materials and chemical processes that can benefit from its unique properties.
Check Digit Verification of cas no
The CAS Registry Mumber 52437-39-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,3 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 52437-39:
(7*5)+(6*2)+(5*4)+(4*3)+(3*7)+(2*3)+(1*9)=115
115 % 10 = 5
So 52437-39-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O/c1-8-4-5-9(6-7-11)10(8,2)3/h4,9,11H,5-7H2,1-3H3/t9-/m1/s1
52437-39-5Relevant articles and documents
HYDROGENATION OF ESTERS OR CARBONYL GROUPS WITH TETRADENTATE AMINO/IMINO-THIOETHER BASED RUTHENIUM COMPLEXES
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Paragraph 0112, (2013/10/22)
The present invention relates to the field of catalytic hydrogenation and, more particularly, to the use of specific ruthenium catalysts, or pre-catalysts, in hydrogenation processes for the reduction of ketones and/or aldehydes into the corresponding alcohol respectively. Said catalysts are ruthenium complexes comprising a tetradentate ligand (L4) coordinating the ruthenium with: two nitrogen atoms, each in the form of a primary or secondary amine (i.e. a NH2 or NH group) or N-alkyl imine functional groups (i.e. a C═N group), and two sulfur atoms, each in the form of thioether functional groups.
Preparation of Campholenal Analogues: Chirons for the Lipophilic Moiety of Sandalwood-Like Odorant Alcohols
Chapuis, Christian,Brauchli, Robert
, p. 1527 - 1546 (2007/10/02)
In connection with structure-activity relationship studies, analogues of campholenal ((+)-4b), an important building block for sandalwood-like odorants, were prepared.The five-membered-ring analogues 4 were obtained by epoxidation of the corresponding α-pinene derivatives 2, followed by catalytic ZnBr2 isomerisation (Scheme 2).The six-membered-ring skeleton was obtained by ozonolysis of α-campholenyl acetate ((-)-14b), followed by intramolecular aldol condensation (Scheme 5). 13C-NMR assignments are given.