4025-69-8 Usage
Description
9,10-dioxo-9,10-dihydroanthracene-1-sulfonyl chloride is a chemical compound with the molecular formula C14H7ClO4S. It is a sulfonyl chloride derivative of anthraquinone, an organic compound widely used in the production of dyes and pigments. This derivative is known for its versatility in organic synthesis, particularly in the preparation of anthraquinone-based dyes and pharmaceuticals. The sulfonyl chloride functional group enables the attachment of the compound to other molecules, making it a valuable reagent in the synthesis of various organic compounds. It can also function as a catalyst in certain organic reactions, contributing to its importance in the field of organic chemistry and its applications in industry and research.
Uses
Used in Organic Synthesis:
9,10-dioxo-9,10-dihydroanthracene-1-sulfonyl chloride is used as a versatile building block for the synthesis of anthraquinone-based dyes and pharmaceuticals. Its sulfonyl chloride functional group allows for the attachment to other molecules, facilitating the creation of a wide range of organic compounds.
Used in Catalyst Applications:
In the field of organic chemistry, 9,10-dioxo-9,10-dihydroanthracene-1-sulfonyl chloride is utilized as a catalyst in certain organic reactions. Its ability to participate in reaction mechanisms enhances the efficiency and selectivity of these processes, making it a valuable tool for chemists.
Used in Dye and Pigment Production:
As a derivative of anthraquinone, 9,10-dioxo-9,10-dihydroanthracene-1-sulfonyl chloride is employed in the production of dyes and pigments. Its unique properties contribute to the development of new dyes with specific characteristics, catering to various industrial needs.
Used in Pharmaceutical Development:
9,10-dioxo-9,10-dihydroanthracene-1-sulfonyl chloride is also used in the pharmaceutical industry for the development of new drugs. Its role in the synthesis of anthraquinone-based pharmaceuticals highlights its potential in creating novel therapeutic agents.
Used in Research:
9,10-dioxo-9,10-dihydroanthracene-1-sulfonyl chloride is a valuable reagent in scientific research, where it is used to explore new chemical reactions and develop innovative synthetic pathways. Its applications in research contribute to the advancement of organic chemistry and related fields.
Check Digit Verification of cas no
The CAS Registry Mumber 4025-69-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,2 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4025-69:
(6*4)+(5*0)+(4*2)+(3*5)+(2*6)+(1*9)=68
68 % 10 = 8
So 4025-69-8 is a valid CAS Registry Number.
4025-69-8Relevant articles and documents
Cationic anthraquinone derivatives as catalytic DNA photonucleases: Mechanisms for DNA damage and quinone recycling
Armitage, Bruce,Yu, Changjun,Devadoss, Chelladurai,Schuster, Gary B.
, p. 9847 - 9859 (2007/10/02)
Ammonium-substituted anthraquinone derivatives have been found to catalyze DNA cleavage upon irradiation with 350 nm light. Picosecond laser spectroscopy demonstrates that the excited quinones react with DNA by two separate oxidative pathways: electron transfer from a nearby base and hydrogen atom abstraction from the deoxyribose component of the nucleic acid backbone. Photo-oxidation of DNA by either pathway yields the one-electron-reduced form of the quinone as a byproduct. Back electron transfer from the reduced quinone to the oxidized base is the predominant decay path for the reduced quinone formed by the electron transfer pathway while that formed by hydrogen atom abstraction is converted back to the ground-state, fully oxidized form by reduction of molecular oxygen. The resulting superoxide anion is detected by its reduction of cytochrome c. Comparison of the spectroscopic data for two quinones with significant different cleavage efficiencies suggests that DNA cleavage by these quinone reagents results from the hydrogen-abstraction chemistry. The laser experiments further indicate that the quinone completes one cycle of excitation, oxidation of DNA, and reduction of oxygen within 10 μs, illustrating the potential utility of these agents for double-stranded cleavage of DNA.
