98102-91-1 Usage
Description
(+/-)-trans-2-Isopropyl-cyclohexanol, also known as dihydrocarvone, is a chiral bicyclic organic compound characterized by its minty, camphor-like odor. It is widely recognized for its applications as a fragrance and flavoring agent in various industries.
Uses
Used in Food Industry:
(+/-)-trans-2-Isopropyl-cyclohexanol is used as a flavoring agent for its minty taste, often incorporated into products such as toothpaste and chewing gum to enhance their flavor profile.
Used in Cosmetic Industry:
In the cosmetic industry, (+/-)-trans-2-Isopropyl-cyclohexanol serves as a fragrance component, adding a refreshing scent to various cosmetic products.
Used in Pharmaceutical Industry:
(+/-)-trans-2-Isopropyl-cyclohexanol is utilized in the production of pharmaceuticals, capitalizing on its unique properties to contribute to the development of medicinal compounds.
Used as a Precursor in Organic Synthesis:
(+/-)-trans-2-Isopropyl-cyclohexanol also acts as a precursor in the synthesis of other organic compounds, highlighting its versatility in organic chemistry.
Used in Health Research:
(+/-)-trans-2-Isopropyl-cyclohexanol has been studied for its potential antimicrobial and antioxidant properties, indicating its possible use in health-related applications and products.
Check Digit Verification of cas no
The CAS Registry Mumber 98102-91-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,1,0 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 98102-91:
(7*9)+(6*8)+(5*1)+(4*0)+(3*2)+(2*9)+(1*1)=141
141 % 10 = 1
So 98102-91-1 is a valid CAS Registry Number.
98102-91-1Relevant articles and documents
Asymmetric Induction via a Helically Chiral Anion: Enantioselective Pentacarboxycyclopentadiene Br?nsted Acid-Catalyzed Inverse-Electron-Demand Diels-Alder Cycloaddition of Oxocarbenium Ions
Gheewala, Chirag D.,Hirschi, Jennifer S.,Lee, Wai-Hang,Paley, Daniel W.,Vetticatt, Mathew J.,Lambert, Tristan H.
supporting information, p. 3523 - 3527 (2018/03/21)
An enantioselective catalytic inverse-electron-demand Diels-Alder reaction of salicylaldehyde acetal-derived oxocarbenium ions and vinyl ethers to generate 2,4-dioxychromanes is described. Chiral pentacarboxycyclopentadiene (PCCP) acids are found to be effective for a variety of substrates. Computational and X-ray crystallographic analyses support the unique hypothesis that an anion with point-chirality-induced helical chirality dictates the absolute sense of stereochemistry in this reaction.
Diastereoselective reduction of cyclohexanones with diisobutylaluminium phenoxides in terms of the isoinversion principle
Meyer-Stork, Markus A.,Haag, Dieter,Scharf, Hans-Dieter
, p. 593 - 595 (2007/10/03)
The diastereoselectivity of the reduction of 2-substituted cyclohexanones 1-6 with 4-substituted diisobutylaluminium phenoxides a-d has been investigated as a function of temperature. The high-temperature region is found to be dominated by hydride transfer, which is controlled by steric as well as electronic effects. However, at low temperatures the Meerwein-Ponndorf-Verley reaction gains in Importance. This phenomenon is quantified by an isoinversion relationship.
