3479-89-8 Usage
Explanation
The compound consists of 10 carbon atoms and 14 hydrogen atoms.
Explanation
The molecule has a seven-membered ring with alternating double and single bonds (a triene) and is in a cyclic arrangement.
Explanation
The molecule has three additional CH3 groups, which are attached to the heptatriene ring at positions 3, 7, and 7.
Explanation
The compound is liquid and colorless under standard conditions, making it easy to handle and observe.
Explanation
The compound exhibits aromatic properties due to its cyclic structure and the presence of double bonds, which contribute to its stability and reactivity.
Explanation
It is used as a starting material for the synthesis of various other organic compounds, making it a valuable intermediate in chemical reactions.
Explanation
The compound serves as a key intermediate in the synthesis of a wide range of organic compounds, highlighting its versatility.
Explanation
Due to its structure and the presence of double bonds, the compound can participate in various chemical reactions, making it a valuable tool in organic chemistry.
Explanation
Despite its reactivity, the compound is relatively stable when stored properly and away from extreme conditions, which allows for its use in various applications.
Structure
Cyclic hydrocarbon with a heptatriene ring
Methyl groups
Three methyl groups attached to different carbon atoms
Physical state
Colorless liquid at room temperature
Aromatic properties
Unique aromatic characteristics
Application
Building block in organic synthesis
Precursor
Important precursor for the preparation of other compounds
Reactivity
Highly reactive
Stability
Relatively stable under normal conditions
Check Digit Verification of cas no
The CAS Registry Mumber 3479-89-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,7 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3479-89:
(6*3)+(5*4)+(4*7)+(3*9)+(2*8)+(1*9)=118
118 % 10 = 8
So 3479-89-8 is a valid CAS Registry Number.
3479-89-8Relevant academic research and scientific papers
Transformations of 3-carene oxide at rhenium-containing catalysts
Manukov, E. N.,Bazhina, G. N.
, p. 106 - 110 (2007/10/02)
The transformations of 3-carene oxide at rhenium-containing catalysts were studied.The introduction of rhenium into the catalytic system significantly increases the reaction rate and leads to the formation of compounds not previously encountered in the products from the isomerization of 3-carene oxide, i.e., 3-carene, 3(10),4-caradiene, 3,3,6-trimethylcycloheptanone, and 3-caren-10-ol.
DISPROPORTIONATION OF HYDROGEN IN 3-CARENE
Manukov, E. N.,Chuiko, V. A.,Vyglazov, O. G.
, p. 257 - 262 (2007/10/02)
The disproportionation of hydrogen in 3-carene takes place with the formation of compounds of the 1,1,4-trimethylcycloheptane series.The proposed reaction mechanism involves dehydration of the 2-carene to 2,4-caradiene, which exists in a rapid tautomeric equilibrium with 3,7,7-trimethyl-1,3,5-cycloheptatriene.This gives rise to the appearance of compounds with a seven-membered ring in the reaction product.
Chemistry of the 2-Pinanols. 2. Investigation of the Utility of the Enhanced Basicities of the Pinanoxide Bases
Traynor, Sean G.,Kane, Bernard J.,Coleman, Jacquelyn B.,Cardenas, Carlos G.
, p. 900 - 906 (2007/10/02)
The utility of the alkoxides of cis- and trans-2-pinanol has been investigated.Yiels comparable to and exceeding those obtained with tert-butoxide are reported for the alkylation of ethyl acetoacetate, for the conversion of α-pinene oxide to trans-pinocarveol and cis-3-pinen-2-ol, and for the isomerization of vinylnorbornene and limonene.Dehydrohalogenation was effected rapidly on bornyl chloride and 2,6-dichlorocamphane-compounds reported to be inert to potassium tert-butoxide in tert-butyl alcohol.Reactions with 1-octyl bromide and with benzyl chloride showed that the pinanoxides have nucleophilicities comparable to that of tert-butoxide.
