130650-84-9 Usage
Chemical Family
Etiochlorin
Etiochloin is a family of chemical compounds that 2,3-dihydroxyetiochlorin belongs to.
Type of Compound
Porphyrin Derivative
2,3-dihydroxyetiochlorin is derived from the porphyrin structure, which is a macrocyclic organic compound.
Hydroxyl Groups
Two
The compound has two hydroxyl groups attached to it, which contribute to its chemical properties and potential applications.
Attachment Positions
Second and Third Positions
The hydroxyl groups are specifically attached to the second and third positions of the etiochlorin ring system.
Potential Application
Photodynamic Therapy
2,3-dihydroxyetiochlorin has been studied for its potential use in photodynamic therapy, a treatment method that targets cancer cells.
Role in Photodynamic Therapy
Photosensitizer
The compound can act as a photosensitizer, which is a substance that absorbs light and becomes excited, enabling it to generate reactive oxygen species.
Mechanism of Action
Reactive Oxygen Species Generation
Upon light activation, 2,3-dihydroxyetiochlorin can generate reactive oxygen species, which are responsible for inducing cell death in targeted cells.
Current Status
Ongoing Research
Research on 2,3-dihydroxyetiochlorin and its potential medicinal and therapeutic uses is still ongoing, with further studies being conducted to explore its full potential.
Check Digit Verification of cas no
The CAS Registry Mumber 130650-84-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,6,5 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 130650-84:
(8*1)+(7*3)+(6*0)+(5*6)+(4*5)+(3*0)+(2*8)+(1*4)=99
99 % 10 = 9
So 130650-84-9 is a valid CAS Registry Number.
InChI:InChI=1/C32H40N4O2/c1-9-20-17(5)23-13-27-21(10-2)19(7)25(35-27)15-30-32(38,12-4)31(8,37)29(36-30)16-28-22(11-3)18(6)24(34-28)14-26(20)33-23/h13-16,34-35,37-38H,9-12H2,1-8H3/b23-13-,24-14-,25-15-,26-14-,27-13-,28-16-,29-16-,30-15-/t31-,32+/m0/s1
130650-84-9Relevant articles and documents
Syntheses of oxygen analogues of sulfhemes-A and -C
Iakovides, Panos,Smith, Kevin M.
, p. 1123 - 1148 (2007/10/03)
Syntheses of metal-free oxygen analogues of the sulfhemes-A and -C from protoporphyrin-IX dimethyl ester I are presented. Oxasulfporphyrin-C dimethyl ester 5 is obtained by intramolecular displacement of a primary tosylate by a tertiary hydroxyl in an appropriately constructed precursor 18, or by surface-catalyzed rearrangement of the epoxide-bearing oxasulfporphyrin-A dimethyl ester 23. Compound 23 is in turn prepared by Mitsunobu type internal dehydration of the precursor 12. The methodology is then successfully extended to more symmetric porphyrin systems. Compounds 23, 25, 46, and 61/62 are the first porphyrin epoxides to be synthesized.
