10210-21-6 Usage
Description
1,3,8-Trihydroxy-6-methoxy-2-(1-oxohexyl)-9,10-anthraquinone is a naturally occurring chemical compound with a complex structure, featuring three hydroxyl groups, a methoxy group, an oxohexyl group, and an anthraquinone core. It is found in plants such as Rubia tinctorum, commonly known as madder.
Uses
Used in Textile Industry:
1,3,8-Trihydroxy-6-methoxy-2-(1-oxohexyl)-9,10-anthraquinone is used as a dye in the textile industry for providing a range of red and orange hues. Its natural origin and vibrant coloration make it a preferred choice for various textile applications.
Used in Pharmaceutical and Nutraceutical Development:
1,3,8-Trihydroxy-6-methoxy-2-(1-oxohexyl)-9,10-anthraquinone is used as a potential medicinal compound for its demonstrated antioxidant and anti-inflammatory effects. It is a subject of interest in the development of pharmaceuticals and nutraceuticals, although 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.
