69480-06-4 Usage
General Description
"Ethanone, 1-(2,6-dihydroxy-4-methoxy-3-methylphenyl)-" is a chemical compound that belongs to the class of keto compounds. It is a derivative of 2,6-dihydroxy-4-methoxy-3-methylphenol, also known as syringic acid. This chemical is commonly used in the field of organic chemistry for various purposes such as organic synthesis, pharmaceutical research, and as a chemical intermediate. It possesses antioxidant properties due to the presence of hydroxyl groups, which make it potentially useful in the development of new drugs or health supplements. Overall, Ethanone, 1-(2,6-dihydroxy-4-methoxy-3-methylphenyl)- is a versatile chemical compound with a wide range of potential applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 69480-06-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,4,8 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 69480-06:
(7*6)+(6*9)+(5*4)+(4*8)+(3*0)+(2*0)+(1*6)=154
154 % 10 = 4
So 69480-06-4 is a valid CAS Registry Number.
69480-06-4Relevant articles and documents
Mallotojaponins B and C: Total Synthesis, Antiparasitic Evaluation, and Preliminary SAR Studies
Grayfer, Tatyana D.,Grellier, Philippe,Mouray, Elisabeth,Dodd, Robert H.,Dubois, Jo?lle,Cariou, Kevin
supporting information, p. 708 - 711 (2016/03/01)
(Chemical Equation Presented). The first total syntheses of mallotojaponin B and C as well as several analogues have been achieved. Biological evaluation of the synthesized compounds against Plasmodium falciparum and Trypanosoma brucei have also been carried out.
Anti-AIDS agents 68. The first total synthesis of a unique potent anti-HIV chalcone from genus Desmos
Nakagawa-Goto, Kyoko,Lee, Kuo-Hsiung
, p. 8263 - 8266 (2007/10/03)
The first total synthesis of a unique highly functionalized and potent anti-HIV chalcone 1, isolated from genus Desmos, was achieved from commercially available 2,4,6-trihydroxytoluene (3) or 2,4,6-trihydroxybenzaldehyde (2) in five (from 3) or six steps (from 2).