10210-21-6 Usage
General Description
1,3,8-Trihydroxy-6-methoxy-2-(1-oxohexyl)-9,10-anthraquinone is a chemical compound with a complex structure consisting of three hydroxyl groups, a methoxy group, an oxohexyl group, and an anthraquinone core. 1,3,8-Trihydroxy-6-methoxy-2-(1-oxohexyl)-9,10-anthraquinone is a naturally occurring pigment found in plants such as Rubia tinctorum, also known as madder. It is commonly used as a dye in the textile industry, providing a range of red and orange hues. Additionally, this compound has demonstrated potential medicinal properties, including antioxidant and anti-inflammatory effects, making it a subject of interest in the development of pharmaceuticals and nutraceuticals. However, further research is needed to fully understand its potential benefits and risks.
Check Digit Verification of cas no
The CAS Registry Mumber 10210-21-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,1 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10210-21:
(7*1)+(6*0)+(5*2)+(4*1)+(3*0)+(2*2)+(1*1)=26
26 % 10 = 6
So 10210-21-6 is a valid CAS Registry Number.
InChI:InChI=1/C21H20O7/c1-3-4-5-6-13(22)18-15(24)9-12-17(21(18)27)20(26)16-11(19(12)25)7-10(28-2)8-14(16)23/h7-9,23-24,27H,3-6H2,1-2H3
10210-21-6Relevant articles and documents
Cycloaddition of cross-conjugated trienes to halogenated quinones
Couturier,Brassard
, p. 703 - 708 (2007/10/02)
The chemoselectivity of [4+2] cycloadditions involving electron-rich cross-conjugated trienes and halogenated quinones has been examined. The approach provides improved preparations of 6-acetyl-2,3,7-trihydroxyjuglone, solorinic and norsolorinic acids, and averythrin. It also confirms the structure proposed for haematommone and 3,8-dihydroxy-4-methoxy-2-methoxycarbonyl-1-methylanthraquinone but invalidates that of sopheranin.
