86456-20-4 Usage
Description
2-(TOLUENE-4-SULFONYLOXY)-8-(2-DIMETHYLAMINO-ETHYLAMINO)-XANTHEN-9-ONE is a chemical compound derived from xanthen-9-one, featuring a toluene-4-sulfonyloxy group at position 2 and a 2-dimethylamino-ethylamino group at position 8 on the xanthene ring. It is known for its fluorescent properties and potential applications in various scientific and medical fields.
Uses
Used in Organic Synthesis and Medicinal Chemistry:
2-(TOLUENE-4-SULFONYLOXY)-8-(2-DIMETHYLAMINO-ETHYLAMINO)-XANTHEN-9-ONE is used as a fluorescent dye for its ability to emit light upon exposure to specific wavelengths, facilitating the study of molecular interactions and processes.
Used in Fluorescence Microscopy:
In the field of fluorescence microscopy, 2-(TOLUENE-4-SULFONYLOXY)-8-(2-DIMETHYLAMINO-ETHYLAMINO)-XANTHEN-9-ONE is used as a molecular probe to visualize cellular structures and processes, enhancing the understanding of biological mechanisms.
Used in Flow Cytometry:
2-(TOLUENE-4-SULFONYLOXY)-8-(2-DIMETHYLAMINO-ETHYLAMINO)-XANTHEN-9-ONE is utilized in flow cytometry as a fluorescent marker to analyze and sort cells based on specific characteristics, aiding in research and diagnostics.
Used in Cell Imaging:
2-(TOLUENE-4-SULFONYLOXY)-8-(2-DIMETHYLAMINO-ETHYLAMINO)-XANTHEN-9-ONE is employed in cell imaging to label and track cellular components, providing insights into cell behavior and function.
Used in Pharmaceutical Development:
2-(TOLUENE-4-SULFONYLOXY)-8-(2-DIMETHYLAMINO-ETHYLAMINO)-XANTHEN-9-ONE is used in the development of new pharmaceuticals, potentially contributing to the creation of drugs with improved targeting and therapeutic effects.
Used in Diagnostic Tool Development:
2-(TOLUENE-4-SULFONYLOXY)-8-(2-DIMETHYLAMINO-ETHYLAMINO)-XANTHEN-9-ONE is also used in the development of diagnostic tools, where its fluorescent properties can be harnessed for detecting and monitoring diseases.
Used in Antiviral Research:
2-(TOLUENE-4-SULFONYLOXY)-8-(2-DIMETHYLAMINO-ETHYLAMINO)-XANTHEN-9-ONE is studied for its potential antiviral properties, exploring its ability to inhibit viral replication and infection.
Used in Anticancer Research:
In the field of oncology, this compound is investigated for its potential anticancer properties, examining its effects on tumor growth and the possibility of integrating it into cancer treatment strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 86456-20-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,4,5 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86456-20:
(7*8)+(6*6)+(5*4)+(4*5)+(3*6)+(2*2)+(1*0)=154
154 % 10 = 4
So 86456-20-4 is a valid CAS Registry Number.
InChI:InChI=1/C24H24N2O5S/c1-16-7-10-18(11-8-16)32(28,29)31-17-9-12-21-19(15-17)24(27)23-20(25-13-14-26(2)3)5-4-6-22(23)30-21/h4-12,15,25H,13-14H2,1-3H3
86456-20-4Relevant articles and documents
Analogues of hycanthone and lucanthone as antitumor agents
Archer,Zayed,Rej,Rugino
, p. 1240 - 1246 (2007/10/02)
Hycanthone analogues (5 and 6) containing 7-substituted hydroxyl groups were prepared and evaluated as antitumor agents. These compounds were significantly more active than the corresponding unsubtituted derivatives. The 7-hydroxylated-4-(hydroxymethyl)-9H-xanthen-9-ones, 11 and 12, were also active antitumor agents. However, the 7-hydroxy-9H-xanthen-9-one counterparts of the 7-hydroxylucanthones were totally devoid of antitumor activity. Results obtained thus far are consistent with the hypothesis that 4-hydroxymethyl substituents in the 9H-xanthen-9-one and 9H-thioxanthen-9-one series are required for antitumor activity.
