179249-41-3 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 10 carbon (C) atoms, 20 hydrogen (H) atoms, and 2 oxygen (O) atoms.
2. Cyclohexane derivative
Explanation
The compound is derived from cyclohexane, which is a six-carbon ring structure. It has additional functional groups attached to the ring.
Explanation
The cyclohexane ring has hydroxyl (-OH) groups attached at the 1st, 2nd, and 4th positions, making it a triol.
4. Isoborneol
Explanation
1,4-Cyclohexanediol,2-(1-methylethyl)-,(1alpha,2alpha,4alpha)-(9CI) is also known as isoborneol, which is a common name for this compound.
Explanation
Isoborneol can be found in the essential oils extracted from specific plants, indicating its natural occurrence.
Explanation
Isoborneol is used as a starting material or intermediate in the synthesis of various chemicals and pharmaceuticals. It also has potential applications in the perfume and flavor industry due to its unique properties.
Explanation
As with any chemical compound, it is important to handle isoborneol with care to avoid potential hazards. This may include following safety guidelines, using appropriate protective equipment, and being aware of its potential health and environmental effects.
Explanation
The stereochemistry of the compound is indicated by the (1alpha,2alpha,4alpha)-(9CI) notation, which describes the spatial arrangement of the hydroxyl groups on the cyclohexane ring. The "alpha" designation refers to the position of the hydroxyl group relative to the ring.
Hydroxyl groups
1, 2, and 4 positions
Occurrence
Essential oils of certain plants
Applications
Synthesis of chemicals, pharmaceuticals, perfume, and flavor industry
Hazards
Proper handling required
Stereochemistry
(1alpha,2alpha,4alpha)-(9CI)
Check Digit Verification of cas no
The CAS Registry Mumber 179249-41-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,2,4 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 179249-41:
(8*1)+(7*7)+(6*9)+(5*2)+(4*4)+(3*9)+(2*4)+(1*1)=173
173 % 10 = 3
So 179249-41-3 is a valid CAS Registry Number.
179249-41-3Relevant articles and documents
Unusual facial selectivity in the cycloaddition of singlet oxygen to a simple cyclic diene
Davis, Kelly M.,Carpenter, Barry K.
, p. 4617 - 4622 (2007/10/03)
Syntheses of 5-isopropyl-1,3-cyclohexadiene and syn-5-isopropyl-2,3-dioxabicyclo[2.2.2]octane, by routes that would allow completely diastereoselective introduction of deuterium labels, are described. The reaction of the isopropyl cyclohexadiene with singlet oxygen is shown to give an endoperoxide that is derived by preferential attack on the more sterically hindered face of the diene. A possible mechanistic explanation of this result is that the attack from the less hindered face leads to "ene" reaction rather than endoperoxide formation. However, this mechanism would require that the "ene" reaction and cycloaddition proceed via a common intermediate-presumably a perepoxide.
