58437-71-1 Usage
Description
(E)-2-(3,3-dimethylbicyclo[2.2.1]hept-2-ylidene)ethanol, with the molecular formula C11H18O, is a colorless liquid chemical compound known for its diverse applications across various industries. It is characterized by its distinct fragrance and flavor, as well as its antibacterial and antifungal properties, making it a valuable ingredient in numerous products.
Uses
Used in Fragrance and Flavor Industry:
(E)-2-(3,3-dimethylbicyclo[2.2.1]hept-2-ylidene)ethanol is used as a fragrance ingredient and flavoring agent for its distinct scent and taste, enhancing the sensory appeal of products in perfumes, cosmetics, and the food industry.
Used in Personal Care Products:
In the personal care industry, (E)-2-(3,3-dimethylbicyclo[2.2.1]hept-2-ylidene)ethanol is used as an active ingredient for its antibacterial and antifungal properties, contributing to the effectiveness of products in maintaining hygiene and preventing infections.
Used in Pharmaceuticals:
(E)-2-(3,3-dimethylbicyclo[2.2.1]hept-2-ylidene)ethanol is utilized in the pharmaceutical industry for its antimicrobial characteristics, playing a role in the development of products aimed at treating bacterial and fungal infections.
Used in Organic Synthesis:
(E)-2-(3,3-dimethylbicyclo[2.2.1]hept-2-ylidene)ethanol is also used as a chiral building block in organic chemistry, facilitating the synthesis of other organic compounds and contributing to the advancement of chemical research and development.
Safety Precautions:
It is crucial to handle and store (E)-2-(3,3-dimethylbicyclo[2.2.1]hept-2-ylidene)ethanol with care, as it can be harmful if ingested, inhaled, or comes into contact with the skin. Proper safety measures should be taken to minimize potential risks.
Check Digit Verification of cas no
The CAS Registry Mumber 58437-71-1 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, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 58437-71:
(7*5)+(6*8)+(5*4)+(4*3)+(3*7)+(2*7)+(1*1)=151
151 % 10 = 1
So 58437-71-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H18O/c1-11(2)9-4-3-8(7-9)10(11)5-6-12/h5,8-9,12H,3-4,6-7H2,1-2H3/b10-5+
58437-71-1Relevant articles and documents
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).
