918-83-2 Usage
Uses
Used in Fragrance Industry:
Geraniol is used as a key component in perfumes, soaps, and lotions due to its pleasant, rose-like scent, enhancing the fragrance of these products and providing a desirable sensory experience for consumers.
Used in Insect Repellent Products:
Leveraging its insect-repellent properties, geraniol is utilized in mosquito repellents and pet flea collars, offering a natural alternative to chemical-based repellents and helping to protect against insect bites and infestations.
Used in Therapeutic Applications:
Geraniol has been studied for its potential therapeutic benefits, including antimicrobial and antioxidant properties. Its antimicrobial activity makes it a candidate for use in sanitizing products, while its antioxidant properties suggest potential applications in skincare and health products to promote overall well-being.
However, it is important to note that geraniol can be an irritant to the skin and respiratory system in high concentrations, necessitating careful consideration in its application and dosage to ensure safety and effectiveness.
Check Digit Verification of cas no
The CAS Registry Mumber 918-83-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,1 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 918-83:
(5*9)+(4*1)+(3*8)+(2*8)+(1*3)=92
92 % 10 = 2
So 918-83-2 is a valid CAS Registry Number.
918-83-2Relevant articles and documents
SnCl2/KI-mediated allylation reactions of formaldehyde in water
Lin, Mei-Huey,Lin, Long-Zhi,Chuang, Tsung-Hsun
supporting information; experimental part, p. 1871 - 1874 (2011/09/16)
An efficient procedure for SnCl2/KI-mediated allylation reactions of formaldehyde with a variety of allylic bromides in aqueous solution is reported. Under conditions developed in this effort, various homoallylic alcohols and 2-halohomoallylic alcohols are produced in good to excellent yields. Georg Thieme Verlag Stuttgart New York.
Intramolecular trapping of an ylide intermediate in the reaction of1:CH2 with an allylic alcohol
Sobery, Warunee,DeLuca, Joann P.
, p. 3315 - 3316 (2007/10/02)
The reaction of 1:CH2, generated by the photolysis of CH2N2, with 2-methyl-3-buten-2-ol leads to the formation of several products including 4-methyl-3-penten-1-ol. This product is best explained as the result of rearrangement of an ylide intermediate.
