52330-11-7 Usage
Uses
Used in Pharmaceutical Industry:
Tricyclo[12.3.1.12,6]nonadeca-1(18),2,4,6(19),10,14,16-heptaen-9-one,3,17-dihydroxy-,(10E)is used as a pharmaceutical compound for its potential therapeutic properties. The presence of hydroxyl groups and the unique structure of the compound may contribute to its bioactivity, making it a candidate for the development of new drugs or drug delivery systems.
Used in Chemical Industry:
In the chemical industry, Tricyclo[12.3.1.12,6]nonadeca-1(18),2,4,6(19),10,14,16-heptaen-9-one,3,17-dihydroxy-,(10E)can be used as a precursor or intermediate in the synthesis of other complex organic compounds. Its unique structure and functional groups may enable the development of novel chemical reactions or processes.
Used in Cosmetic Industry:
Tricyclo[12.3.1.12,6]nonadeca-1(18),2,4,6(19),10,14,16-heptaen-9-one,3,17-dihydroxy-,(10E)'s potential color and stability properties make it a candidate for use in the cosmetic industry. Tricyclo[12.3.1.12,6]nonadeca-1(18),2,4,6(19),10,14,16-heptaen-9-one,3,17-dihydroxy-,(10E)can be used as a natural colorant or additive in cosmetic products, providing a vibrant and visually appealing appearance.
Used in Food Industry:
Due to its carotenoid origin and potential color properties, Tricyclo[12.3.1.12,6]nonadeca-1(18),2,4,6(19),10,14,16-heptaen-9-one,3,17-dihydroxy-,(10E)may be utilized in the food industry as a natural colorant or additive. Its unique structure and properties could contribute to the development of new food products with enhanced visual appeal and nutritional value.
Used in Research and Development:
The unique structure and properties of Tricyclo[12.3.1.12,6]nonadeca-1(18),2,4,6(19),10,14,16-heptaen-9-one,3,17-dihydroxy-,(10E)make it an interesting subject for research and development in various scientific fields. It can be used as a model compound to study the properties and behavior of tetraterpenoids and carotenoids, as well as to explore new applications and potential benefits in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 52330-11-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,3 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 52330-11:
(7*5)+(6*2)+(5*3)+(4*3)+(3*0)+(2*1)+(1*1)=77
77 % 10 = 7
So 52330-11-7 is a valid CAS Registry Number.
52330-11-7Relevant academic research and scientific papers
Reaction of Aryl and Vinyl Halides with Zerovalent Nickel-Preparative Aspects and the Synthesis of Alnusone
Semmelhack, M.F.,Helquist, Paul,Jones, L.D.,Keller, Leonard,Mendelson L.,et al.
, p. 6460 - 6471 (2007/10/02)
Zerovalent nickel complexes such as bis(1,5-cyclooctadiene)nickel and tetrakis(triphenylphosphine)nickel react rapidly with aryl and vinyl halides to produce the symmetrical coupling products, a low-temperature analogue of the Ullman reaction.The reaction proceeds through oxidative addition of the organic halide to Ni(0), and the reactivity of the Ni(II)intermediates has been examined.Arylnickel halide complexes decompose rapidly to biaryls in DMF.The coupling of simple vinyl halides proceeds with isomerization of the double bond but 3-haloacrylates give efficient co upling with retention of geometry.Cyclizations to form ortho-bridged biaryls are efficient in simple cases (6-, 7-, 8-, 9-, 10-, and 14-membered rings) but fail with an ortho-disubstituted case.The 13-membered meta-bridged cyclic biphenyl, alnusone, is prepared efficiently with the crucial aryl halide coupling to form the ring proceeding in 50percent yield.A side reaction promoted by the presence of protons and with certain ortho-substituted aryl halides is reduction of the aryl halide to the arene.This process can be enhanced by deliberate addition of acid during reaction with Ni(0) and a series of aryl halides underwent succesful reduction.
