212513-35-4 Usage
Molecular structure
1H-Indene-4,6-diol,2-(3,5-dihydroxyphenyl)-2,3-dihydro-3-(4-hydroxyphenyl)-1-[(4-hydroxyphenyl)methylene]-,(1Z,2R,3R)-rel-()-
Explanation
The compound has a complex structure with multiple functional groups and a specific arrangement of atoms.
Explanation
The compound has a specific stereochemistry, meaning it cannot be superimposed on its mirror image.
Explanation
The compound's complex structure and properties make it suitable for various organic synthesis reactions.
Explanation
The presence of hydroxyl groups and phenyl rings in the structure contributes to its potential antioxidant and radical scavenging properties.
Explanation
The compound's unique structure and properties may make it valuable in the development of pharmaceuticals and drugs.
Explanation
The compound exists as an enantiomer with negative optical rotation, which can be important for its biological activity and interactions with other molecules.
Chiral molecule
(1Z,2R,3R) prefix
Usage in organic chemistry
Mainly used in the field of organic chemistry
Antioxidant and radical scavenging properties
Contains several hydroxyl groups and phenyl rings
Value in pharmaceuticals and drug development
Specific structure and properties
Optical activity
(-) enantiomer
Check Digit Verification of cas no
The CAS Registry Mumber 212513-35-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,2,5,1 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 212513-35:
(8*2)+(7*1)+(6*2)+(5*5)+(4*1)+(3*3)+(2*3)+(1*5)=84
84 % 10 = 4
So 212513-35-4 is a valid CAS Registry Number.
