13794-73-5 Usage
Description
[3R-(3alpha,3abeta,6alpha,7beta,8aalpha)]-hexahydro-3,6,8,8-tetramethyl-1H-3a,7-methanoazulen-5(4H)-one is a complex chemical compound belonging to the class of azulenones, derived from the azulene molecule. It is a yellow-brown solid with a distinctive odor and is known for its unique chemical properties and potential biological activities.
Uses
Used in Synthetic Organic Chemistry:
[3R-(3alpha,3abeta,6alpha,7beta,8aalpha)]-hexahydro-3,6,8,8-tetramethyl-1H-3a,7-methanoazulen-5(4H)-one is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for the development of new molecules with potential applications in different fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, [3R-(3alpha,3abeta,6alpha,7beta,8aalpha)]-hexahydro-3,6,8,8-tetramethyl-1H-3a,7-methanoazulen-5(4H)-one is used as a starting material for the development of new drugs. Its potential biological activities make it an interesting candidate for researchers working on medicinal chemistry and drug discovery.
Used in Material Science:
[3R-(3alpha,3abeta,6alpha,7beta,8aalpha)]-hexahydro-3,6,8,8-tetramethyl-1H-3a,7-methanoazulen-5(4H)-one is also utilized in material science for the creation of novel materials with specific properties. Its unique chemical structure contributes to the development of advanced materials for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 13794-73-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,9 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13794-73:
(7*1)+(6*3)+(5*7)+(4*9)+(3*4)+(2*7)+(1*3)=125
125 % 10 = 5
So 13794-73-5 is a valid CAS Registry Number.
13794-73-5Relevant articles and documents
Cedar camphor derivative as well as preparation method and application thereof
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Paragraph 0063-0066, (2021/04/03)
The invention relates to the technical field of synthetic drugs, in particular to a cedar camphor derivative as well as a preparation method and an application thereof. The cedar camphor derivative isany one of compounds shown in the following structural formula, tautomers, hydrates, solvates or pharmaceutically acceptable salts thereof, and the cedar camphor derivative has a good treatment effect on viruses, especially influenza viruses, so that the application range of the cedar camphor and the derivatives thereof is expanded, and the variety of the cedar camphor derivatives is expanded.
THE STEREOCHEMISTRY OF PIPITZOLS AND PEREZOLS
Joseph-Nathan, P.,Roman, L. U.,Hernandez, J. D.,Taira, Z.,Watson, W. H.
, p. 731 - 734 (2007/10/02)
The stereochemistry of α-pipitzol (1a) has been established by transformation to cedrene (4) and by single cristal X-ray diffraction of α-pipitzol benzoate (1b).The stereochemistries of the related cedranolides β-pipitzol (2a), α-(1c), β-(2c) and γ-perezol (1d) are assigned from their respective ORD curves.
