678159-56-3 Usage
Bicyclic diol structure
The compound has two interconnected rings, with two hydroxyl (OH) groups attached.
Methyl group
A single carbon atom (-CH3) is attached to the cyclohexane ring.
Methoxy group
An oxygen atom bonded to a methyl group (-O-CH3) is attached to the cyclohexane ring.
Isopropenyl group
A three-carbon group with a double bond between the first and second carbon atoms (-C(CH3)=CH2) is attached to the cyclohexane ring.
Stereoisomers
The compound is a mixture of four stereoisomers, which are different spatial arrangements of the same molecular formula.
(1R,2R,3S,6R)-rel configuration
The most common stereoisomer has this specific arrangement of the atoms in the molecule.
Applications
Used in the production of pharmaceuticals, fragrances, and other organic compounds.
Organic synthesis
The compound has potential applications in the field of organic synthesis, which involves the formation of new chemical compounds from simpler ones.
Biological activity
The compound may have biological activity in certain contexts, but more research is needed to fully understand its properties and potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 678159-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,8,1,5 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 678159-56:
(8*6)+(7*7)+(6*8)+(5*1)+(4*5)+(3*9)+(2*5)+(1*6)=213
213 % 10 = 3
So 678159-56-3 is a valid CAS Registry Number.
678159-56-3Relevant articles and documents
Acid-catalyzed reactions of 2,3-epoxy derivatives of citral with alcohols
Yarovaya,Korchagina,Salomatina,Polovinka,Barkhash
, p. 985 - 991 (2003)
Acid-catalyzed reactions of 2,3-epoxy derivatives of citral (which is a widely spread naturally occurring unsaturated aldehyde) with alcohols were studied under conditions of heterogeneous catalysis and in fluorosulfonic acid. A number of new products were obtained, and possible mechanisms of their formation were proposed.
