392300-29-7 Usage
Explanation
The molecular formula represents the number of carbon (C), hydrogen (H), and oxygen (O) atoms in the compound.
Explanation
1,2,3-Cyclohexanetriol, 2-(2-propenyl)-, 1-acetate, (1S,2R,3R)(9CI) is derived from cyclohexanetriol, which is a naturally occurring compound in some plants.
Explanation
The 1-acetate part of the compound refers to the presence of an acetate functional group (CH3COO-) attached to the molecule.
Explanation
The (1S,2R,3R) configuration specifies the spatial arrangement of the atoms in the molecule, which is important for its chemical properties and potential applications.
Explanation
Due to its unique structure and properties, 1,2,3-Cyclohexanetriol, 2-(2-propenyl)-, 1-acetate, (1S,2R,3R)- (9CI) may have potential uses in the development of pharmaceuticals, as well as in the flavors and fragrances industry.
Explanation
As with many chemicals, 1,2,3-Cyclohexanetriol, 2-(2-propenyl)-, 1-acetate, (1S,2R,3R)(9CI) may pose potential health risks, and it is important to handle and use it with care to minimize any hazards.
Derivative of cyclohexanetriol
Naturally occurring compound found in certain plants
2-(2-propenyl) moiety
Presence of a propenyl group
1-acetate group
Presence of an acetate functional group
(1S,2R,3R) configuration
Stereochemistry of the compound
Applications
Pharmaceuticals, flavors, and fragrances
Health hazards
Handle and use with caution
Check Digit Verification of cas no
The CAS Registry Mumber 392300-29-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,2,3,0 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 392300-29:
(8*3)+(7*9)+(6*2)+(5*3)+(4*0)+(3*0)+(2*2)+(1*9)=127
127 % 10 = 7
So 392300-29-7 is a valid CAS Registry Number.
392300-29-7Relevant articles and documents
Lipase-catalyzed asymmetrization of diacetate of meso-2-(2-propynyl)cyclohexane-l,2,3-triol toward the total synthesis of aquayamycin
Matsumoto,Konegawa,Yamaguchi,Nakamura,Sugai,Suzuki
, p. 1650 - 1652 (2007/10/03)
The diacetate of meso-2-(2-propynyl)cyclohexane-1,2,3-triol was efficiently asymmetrized by hydrolysis with Candida antarctica lipase to give the corresponding mono-acetate in enantiomerically pure form, which was used as the starting material for the total synthesis of aquayamycin. Application of the protocol to the related cyclohexanetriols is also described.
