68330-44-9 Usage
Description
(1S)-EXO-1,2,7,7-TETRAMETHYLBICYCLO[2.2.1]HEPTAN-2-OL is a bicyclic terpene alcohol with the molecular formula C10H20O. It is a colorless liquid with a characteristic odor and is commonly found in the fragrance and flavor industries.
Uses
Used in Fragrance Industry:
(1S)-EXO-1,2,7,7-TETRAMETHYLBICYCLO[2.2.1]HEPTAN-2-OL is used as a key ingredient in the production of perfumes for its unique and characteristic odor.
Used in Flavor Industry:
(1S)-EXO-1,2,7,7-TETRAMETHYLBICYCLO[2.2.1]HEPTAN-2-OL is used as a key ingredient in the production of flavorings for its unique and characteristic odor.
Used in Cosmetics Industry:
(1S)-EXO-1,2,7,7-TETRAMETHYLBICYCLO[2.2.1]HEPTAN-2-OL is used as a key ingredient in the production of cosmetics for its unique and characteristic odor.
Used in Traditional Medicine:
(1S)-EXO-1,2,7,7-TETRAMETHYLBICYCLO[2.2.1]HEPTAN-2-OL is used for its potential therapeutic benefits due to its various biological activities, including antimicrobial, anti-inflammatory, and antioxidant properties.
Check Digit Verification of cas no
The CAS Registry Mumber 68330-44-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,3,3 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 68330-44:
(7*6)+(6*8)+(5*3)+(4*3)+(3*0)+(2*4)+(1*4)=129
129 % 10 = 9
So 68330-44-9 is a valid CAS Registry Number.
68330-44-9Relevant articles and documents
Regiodivergent Hydroborative Ring Opening of Epoxides via Selective C-O Bond Activation
Magre, Marc,Paffenholz, Eva,Maity, Bholanath,Cavallo, Luigi,Rueping, Magnus
supporting information, p. 14286 - 14294 (2020/09/15)
A magnesium-catalyzed regiodivergent C-O bond cleavage protocol is presented. Readily available magnesium catalysts achieve the selective hydroboration of a wide range of epoxides and oxetanes yielding secondary and tertiary alcohols in excellent yields and regioselectivities. Experimental mechanistic investigations and DFT calculations provide insight into the unexpected regiodivergence and explain the different mechanisms of the C-O bond activation and product formation.
Synthesis of 2,2,-Disubstituted Oxetanes from Ketones with S-Methyl-S-(sodiomethyl)-N-(4-tolylsulfonyl)sulfoximine
Welch, Steven C.,Rao, A. S. C. Prakasa,Lyon, John T.,Assercq, Jean-Marie
, p. 252 - 257 (2007/10/02)
A covenient and facile one-step synthesis of 2,2-disubstituted oxetanes from ketones utilizing S-methyl-S-(sodiomethyl)-N-(4-tolylsulfonyl)sulfoxymine in dimethyl sulfoxide is presented.The stereochemistry and chemical reactivity of some 2,2-disubstituted