84560-00-9 Usage
Uses
Used in Fragrance Industry:
2-pentylcyclopentan-1-ol is used as a fragrance ingredient for its pleasant, fruity odor, making it a preferred choice for enhancing the aroma of perfumes, soaps, and other personal care products.
Used in Food Industry:
2-pentylcyclopentan-1-ol is used as a flavoring agent in food products, adding a fruity taste and aroma to various consumer goods.
Used in Personal Care Products:
2-pentylcyclopentan-1-ol is used as a fragrance ingredient in personal care products, providing a pleasant, fruity scent and enhancing the overall sensory experience of these products.
Its low toxicity and natural occurrence in fruits and plants make 2-pentylcyclopentan-1-ol a safe and preferred choice for use in these applications.
Check Digit Verification of cas no
The CAS Registry Mumber 84560-00-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,5,6 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 84560-00:
(7*8)+(6*4)+(5*5)+(4*6)+(3*0)+(2*0)+(1*0)=129
129 % 10 = 9
So 84560-00-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H20O/c1-2-3-4-6-9-7-5-8-10(9)11/h9-11H,2-8H2,1H3
84560-00-9Relevant academic research and scientific papers
Kusumoto, Tetsuo,Ogino, Kumiko,Hiyama, Tamejiro,Isozaki, Tadaaki,Suzuki, Yoshiichi
, p. 865 - 866 (1996)
Liquid crystalline compound having a chiral trans-2-pentylcyclopentyl ester group exhibited stable antiferroelectric chiral smectic C phase whereas its its isomer showed an unidentified smectic phase.
Colloidal palladium nanoparticles with in situ H2: Reducing system for ,-unsaturated carbonyl compounds
De Castro, Kathlia A.,Oh, Seungchan,Yun, Jongchan,Lim, Jin Kyu,An, Gwangil,Kim, Dong Kook,Rhee, Hakjune
experimental part, p. 3509 - 3520 (2009/12/05)
A new reducing system comprising Pd(OAc)2 and NaBH4 in methanol to generate palladium nanoparticles has been efficiently utilized to reduce a variety of unsaturated carbonyl compounds. These were reduced to their corresponding saturated alcohols and fully saturated compounds in selected cases. This protocol presents alternative and mild reaction conditions for reduction.
