58437-69-7 Usage
Uses
Used in the Fragrance Industry:
(E)-2-(3,3-dimethylbicyclo[2.2.1]hept-2-ylidene)ethyl acetate is used as a fragrance ingredient for its distinctive fruity scent. It is commonly employed in the creation of perfumes and colognes, adding a pleasant and appealing aroma to these products.
Used in the Food Industry:
In the food industry, (E)-2-(3,3-dimethylbicyclo[2.2.1]hept-2-ylidene)ethyl acetate is used as a flavoring agent. Its fruity odor makes it a valuable addition to the development of various food products, enhancing their taste and overall sensory experience.
Used in the Cosmetics and Personal Care Industry:
(E)-2-(3,3-dimethylbicyclo[2.2.1]hept-2-ylidene)ethyl acetate is also utilized in the manufacturing of cosmetics and personal care products. Its fruity scent and ability to blend well with other ingredients make it a popular choice for adding a pleasant fragrance to these products.
Used in the Pharmaceutical Industry:
As an intermediate in the synthesis of various pharmaceuticals and other organic compounds, (E)-2-(3,3-dimethylbicyclo[2.2.1]hept-2-ylidene)ethyl acetate plays a crucial role in the development of new drugs and medicinal products. Its unique chemical structure allows for its use in creating a wide range of therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 58437-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,4,3 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 58437-69:
(7*5)+(6*8)+(5*4)+(4*3)+(3*7)+(2*6)+(1*9)=157
157 % 10 = 7
So 58437-69-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H20O2/c1-9(14)15-7-6-12-10-4-5-11(8-10)13(12,2)3/h6,10-11H,4-5,7-8H2,1-3H3/b12-6+
58437-69-7Relevant academic research and scientific papers
ω-Methylcamphene/ω,ω-Dimethylcamphene: Synthesis and Reactions
Lamture, J. B.,Nayak, U. R.
, p. 853 - 858 (2007/10/02)
ω-Methylcamphene (8)/ω,ω-Dimethylcamphene (9) have been synthesized by two routes; (i) the Prins reaction on camphene (1)/ω-methylcamphene (8) and (ii) olefination with methylenetriphenylphosphorane of the aldehyde (17)/methyl ketone (24) followed by isomerization of the resulting hydrocarbon with N-lithioethylenediamine.Camphenilone (2) also undergoes a direct Wittig reaction with ethylidenephosphorane (27) yielding 8 (E/Z)-mixture but fails to react with isopropylidenephosphorane (28) in an attempt to generate 9.Camphene (1) and its ω-methyl homologues 8/9 undergo normal epoxidation with perbenzoic acid without excess consumption of peracid.Lewis acid-catalyzed rearrangement of the resulting epoxides 16/23/29 has also been studied.The Hg(OAc)2/NaCl reaction on 8 yields the crystalline ω-methyl-ω-mercurichloride (10) transformed by pyridine perbromide into the ω-bromo-ω-methylcamphene (11).
Ectocyclic Methylene-Manganic Acetate Reaction: A Comparative Study with Camphene/Longifolene
Goudgaon, N. M.,Nayak, U. R.
, p. 955 - 956 (2007/10/02)
Manganic acetate oxidation has been extended to ectocyclic methylene bridged systems of the type exemplified by camphene (1) and longifolene (2).In the case of 2 the reaction is completely abnormal, resulting in ω-acetoxy-methylation of the olefin without any lactone formation at all.On the other hand, the camphene-Mn(III) acetate reaction yields a mixture of γ-lactone (4) (50percent) and ω-acetoxymethylcamphene (3) (20percent).
