476-43-7 Usage
Description
Cynodontin, a secondary fungal metabolite and dyestuff intermediate, is a compound with notable antifungal properties. It is derived from certain fungi and has the potential to be utilized in various applications due to its inherent characteristics.
Uses
Used in Pharmaceutical Industry:
Cynodontin is used as an antifungal agent for treating a variety of fungal infections. Its antifungal properties make it a valuable asset in combating fungal pathogens that can cause diseases in humans, animals, and plants.
Used in Textile Industry:
As a dyestuff intermediate, Cynodontin plays a crucial role in the production of dyes used in the textile industry. Its ability to contribute to the development of colorants for fabrics makes it an important component in the manufacturing process of textiles.
Used in Agricultural Industry:
Cynodontin can be employed as a protective agent in agriculture to guard crops against fungal diseases. By incorporating this compound into agricultural practices, it can help maintain crop health and increase yield by reducing the impact of fungal infections.
These applications highlight the versatility of Cynodontin and its potential to contribute to various industries beyond its primary function as an antifungal agent.
Check Digit Verification of cas no
The CAS Registry Mumber 476-43-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 476-43:
(5*4)+(4*7)+(3*6)+(2*4)+(1*3)=77
77 % 10 = 7
So 476-43-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H10O6/c1-5-4-8(18)11-12(13(5)19)15(21)10-7(17)3-2-6(16)9(10)14(11)20/h2-4,16-19H,1H3
476-43-7Relevant articles and documents
Regiospecific Synthesis of Quinizarin and Naphthazarin Derivatives by Cycloaddition
Cameron, Donald W.,Feutrill, Geoffrey I.,McKay, Peter G.
, p. 2095 - 2109 (2007/10/02)
The diene (E)-1,1,4-trimethoxybuta-1,3-diene underwent regiospecific cycloaddition to derivatives of 2(3)-chloro-1,4-naphthoquinone.The resulting adducts were aromatized to give 1,4-dioxygenated anthraquinones.The latter were obtained as derivatives of quinizarin dimethyl ether or of quinizarin monomethyl ether depending on the conditions of aromatization.Cycloaddition of the diene to non-halogenated naphthoquinones proceeded similarly, orientation being controlled by substituents in the benzenoid ring.Analogous reaction of the diene with benzoquinones gave 5,8-dioxygenated naphthoquinones (naphthazarins), generally in limited yield.The procedure has been applied to synthesis of the mould metabolites helminthosporin and cynodontin
REGIOSPECIFIC SYNTHESIS OF QUINIZARIN DERIVATIVES BY CYCLOADDITION
Cameron, Donald W.,Feutrill, Geoffrey I.,McKay, Peter G.
, p. 701 - 702 (2007/10/02)
Cycloaddition of (E)-1,1,4-trimethoxy-1,3-butadiene (1) to naphthoquinones affords regiospecific syntheses of derivatives of 1,4-dihydroxyanthraquinone including the mould metabolites helminthosporin (21) and cynodontin (22).
