7540-51-4 Usage
Description
BETA-RHODINOL is a chemical compound with a specific molecular structure that exhibits unique properties and characteristics. It is known for its potential applications in various industries due to its distinct chemical and physical properties.
Uses
Used in Fragrance Industry:
BETA-RHODINOL is used as a fragrance ingredient for its ability to impart a pleasant and distinctive scent to various products. Its unique chemical composition contributes to the overall aroma profile of perfumes, cosmetics, and other fragranced products.
Used in Pharmaceutical Industry:
BETA-RHODINOL is used as an active pharmaceutical ingredient for its potential therapeutic effects. Its specific molecular structure allows it to interact with biological targets, making it a promising candidate for the development of new drugs and treatments.
Used in Chemical Research:
BETA-RHODINOL is used as a research compound in the field of chemistry. Its unique properties make it an interesting subject for studying various chemical reactions and processes, contributing to the advancement of scientific knowledge in this area.
Used in Analytical Chemistry:
BETA-RHODINOL is used as a reference material or standard in analytical chemistry. Its well-defined chemical and physical properties make it suitable for calibrating instruments and ensuring the accuracy of analytical measurements.
Flammability and Explosibility
Notclassified
Check Digit Verification of cas no
The CAS Registry Mumber 7540-51-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,4 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7540-51:
(6*7)+(5*5)+(4*4)+(3*0)+(2*5)+(1*1)=94
94 % 10 = 4
So 7540-51-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H20O/c1-9(2)5-4-6-10(3)7-8-11/h5,10-11H,4,6-8H2,1-3H3/t10-/m1/s1
7540-51-4Relevant articles and documents
Nickel Hydride Catalyzed Cleavage of Allyl Ethers Induced by Isomerization
Kathe, Prasad M.,Berkefeld, Andreas,Fleischer, Ivana
supporting information, p. 1629 - 1632 (2021/02/09)
This report discloses the deallylation of O - and N -allyl functional groups by using a combination of a Ni-H precatalyst and excess Bronsted acid. Key steps are the isomerization of the O - or N -allyl group through Ni-catalyzed double-bond migration followed by Bronsted acid induced O/N-C bond hydrolysis. A variety of functional groups are tolerated in this protocol, highlighting its synthetic value.
Exploration of the Fluoride Reactivity of Aryltrifluoroborate on Selective Cleavage of Diphenylmethylsilyl Groups
Fujiki, Katsumasa,Tanaka, Katsunori
supporting information, p. 4616 - 4620 (2020/07/06)
The first known report on the fluoride catalytic reactivity of potassium aryltrifluoroborate is described. The fluoride reactivity of phenyltrifluoroborate was controlled by substituents on the trifluoroborate-attached benzene, such as the methoxy group a
Total Syntheses of C60- And C100-Dolichols
Hirao, Kohtaro,Ono, Risako,Manabe, Yoshiyuki,Masui, Seiji,Atomi, Haruyuki,Fukase, Koichi
, p. 11549 - 11559 (2020/10/12)
C60- and C100-dolichols were synthesized. A Z-selective Wittig reaction was achieved with high selectivity in a microflow system to realize the scalable supply of the Z-isoprene unit. An isoprene chain was efficiently elongated by an SN2-type coupling between allyl sulfone and allyl chloride using t-BuOK. These key reactions enabled the efficient syntheses of dolichols. This study will pave the way for the functional studies of dolichols.