4354-58-9 Usage
Description
6-cyclohexylhexan-1-ol is a chemical compound with the molecular formula C12H24O. It is a colorless liquid with a slightly floral odor and is known for its mild, pleasant scent.
Uses
Used in Fragrance Industry:
6-cyclohexylhexan-1-ol is used as a fragrance ingredient in perfumes and personal care products for its ability to add a subtle, sweet note to fragrances.
Used in Pharmaceutical Industry:
6-cyclohexylhexan-1-ol has potential applications in the production of pharmaceuticals, where it can be utilized in the development of various medicinal compounds.
Used in Pesticide Industry:
6-cyclohexylhexan-1-ol also has potential applications in the production of pesticides, where it can be used in the formulation of different agrochemical products.
Used as a Solvent:
6-cyclohexylhexan-1-ol can act as a solvent in various industrial applications, providing a medium for dissolving other substances.
Used as a Flavoring Agent:
Additionally, it can be used as a flavoring agent in food products, enhancing the taste and aroma of various consumables.
Safety Precautions:
Although 6-cyclohexylhexan-1-ol is generally considered safe for use in consumer products, it should be handled and stored with proper care due to its flammable nature.
Check Digit Verification of cas no
The CAS Registry Mumber 4354-58-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,5 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4354-58:
(6*4)+(5*3)+(4*5)+(3*4)+(2*5)+(1*8)=89
89 % 10 = 9
So 4354-58-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H24O/c13-11-7-2-1-4-8-12-9-5-3-6-10-12/h12-13H,1-11H2
4354-58-9Relevant articles and documents
Free-radical anti-Markovnikov hydroalkylation of unactivated alkenes with simple alkanes
Tian, Yunfei,Ling, Anbo,Fang, Ren,Tan, Ren Xiang,Liu, Zhong-Quan
supporting information, p. 3432 - 3435 (2018/08/07)
A Cu(ii)-mediated radical anti-Markovnikov hydroalkylation of unactivated alkenes with simple alkanes via selective C(sp3)-H bond cleavage was achieved. This reaction features high site-selectivity diverse functional group tolerance, and scalability.
Synthesis of diaminobutane derivatives as potent Ca2+-permeable AMPA receptor antagonists
Yoneda, Yoshiyuki,Kawajiri, Shinichi,Sugimura, Masunobu,Osanai, Ken,Kito, Fusako,Ota, Emi,Mimura, Tetuya
, p. 2663 - 2666 (2007/10/03)
We synthesized diaminobutane derivatives as potent Ca2+-permeable AMPA receptor antagonists with non-hypotensive activity. Compound 10c showed selective Ca2+-permeable AMPA receptor antagonist activity and neuroprotective effects in transient global ischemia models in gerbils.
