80434-33-9 Usage
General Description
Gamma-diasarone is a chemical compound that belongs to the class of compounds known as alpha,beta-unsaturated aldehydes, which are organic compounds containing a carboxylic group with the formula -C(C=O)H. It is a yellow liquid with a strong, pungent odor and is most commonly used in the synthesis of organic materials and in chemical research. Gamma-diasarone has been studied for its potential applications in the field of medicine, particularly for its antioxidant and anti-inflammatory properties. It is also used as a flavoring agent in the food industry and as a fragrance in the cosmetic industry. However, gamma-diasarone is known to be a skin and eye irritant, and caution should be taken when handling this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 80434-33-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,4,3 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 80434-33:
(7*8)+(6*0)+(5*4)+(4*3)+(3*4)+(2*3)+(1*3)=109
109 % 10 = 9
So 80434-33-9 is a valid CAS Registry Number.
80434-33-9Relevant articles and documents
Pd-Catalyzed Nazarov-Type Cyclization: Application in the Total Synthesis of β-Diasarone and Other Complex Cyclopentanoids
Singh, Bara,Bankar, Siddheshwar K.,Ramasastry
supporting information, p. 1043 - 1048 (2022/02/05)
We describe the palladium-catalyzed Nazarov-type cyclization of easily accessible (hetero)arylallyl acetates to pentannulated (hetero)arenes. This method provides ready access to various types of bi-, tri-, tetra-, and pentacyclic cyclopentanoids under ne
Gold-Catalyzed Dimeric Cyclization of Isoeugenol and Related 1-Phenylpropenes in Ionic Liquid: Environmentally Friendly and Stereoselective Synthesis of 1,2,3-Trisubstituted 2,3-Dihydro-1 H -indenes
Morita, Nobuyoshi,Mashiko, Rie,Hakuta, Dai,Eguchi, Daisuke,Ban, Shintaro,Hashimoto, Yoshimitsu,Okamoto, Iwao,Tamura, Osamu
, p. 1927 - 1933 (2016/07/06)
Gold-catalyzed dimerization of isoeugenol and related 1-phenylpropenes in ionic liquid enabled environmentally friendly, stereoaselective synthesis of 1,2,3-trisubstituted 2,3-dihydro-1H-indenes. Dimerization of isoeugenol or isohomogenol afforded diisoeu
