69745-49-9 Usage
Uses
Used in Industrial Processes:
2,3,3-Trimethylcyclohexene is used as a solvent in industrial processes due to its ability to dissolve a wide range of substances. Its solubility properties make it a valuable component in various manufacturing operations.
Used in Chemical Synthesis:
As an intermediate in the chemical synthesis of other organic compounds, 2,3,3-Trimethylcyclohexene plays a crucial role in the production of various chemical products. Its reactivity and structural features allow it to participate in multiple chemical reactions, contributing to the formation of desired end products.
Used in Fragrance Industry:
2,3,3-Trimethylcyclohexene is utilized as a fragrance ingredient in perfumes and personal care products. Its strong odor and stability make it a suitable candidate for enhancing the scent profiles of various consumer products.
Safety Considerations:
Given its flammability, 2,3,3-Trimethylcyclohexene should be handled with caution to prevent accidents and ensure safe usage in all applications. Proper safety measures and handling protocols should be followed to mitigate risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 69745-49-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,4 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69745-49:
(7*6)+(6*9)+(5*7)+(4*4)+(3*5)+(2*4)+(1*9)=179
179 % 10 = 9
So 69745-49-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H16/c1-8-6-4-5-7-9(8,2)3/h6H,4-5,7H2,1-3H3
69745-49-9Relevant articles and documents
ANHYDROUS FERRIC CHLORIDE DISPERSED ON SILICA GEL INDUCED RING ENLARGEMENT OF TERTIARY CYCLOALKANOLS II: A CONVENIENT HOMOLOGATION OF CYCLOALKANONES, PREPARATION OF SPIRO SYSTEMS AND PROPELLA-γ-LACTONES
Fadel, A.,Salaun, J.
, p. 1267 - 1276 (2007/10/02)
The reagent obtained by mixing anhydrous FeCl3 and silica gel induced, in the lack of any solvent, dehydration of tertiary cycloalkanols, specific C4-->C5 and C5-->C6 ring enlargement, formation of spiro compounds and propella-γ-lactones and cleavage of tetrahydropyranyl ethers.
