14686-65-8 Usage
Uses
Used in Pharmaceutical Research and Medicinal Chemistry:
9H-Xanthen-9-one, 1,5-dihydroxyis used as a key intermediate in the synthesis of various pharmaceutical compounds for its potential therapeutic effects. Its antioxidant properties make it a candidate for the development of drugs targeting oxidative stress-related conditions.
Used in Anticancer Applications:
In the field of oncology, 9H-Xanthen-9-one, 1,5-dihydroxyis utilized as a potential anticancer agent, being studied for its ability to inhibit the growth of cancer cells. It is particularly relevant in the search for novel treatments that can combat the progression of various types of cancer.
Used in the Development of New Materials:
9H-Xanthen-9-one, 1,5-dihydroxyis employed in material science for the creation of new compounds with unique properties. Its role in this industry is to contribute to the advancement of material technologies that can have applications in different sectors.
Used in Organic Optoelectronics:
In the optoelectronics industry, 9H-Xanthen-9-one, 1,5-dihydroxyis used as a component in the development of organic electronic devices. Its光电特性 (photoelectric properties) make it suitable for applications such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs), where its properties can enhance device performance and efficiency.
Overall, 9H-Xanthen-9-one, 1,5-dihydroxydemonstrates a broad spectrum of applications across various industries, underscoring its significance in contemporary scientific research and technological innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 14686-65-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,8 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14686-65:
(7*1)+(6*4)+(5*6)+(4*8)+(3*6)+(2*6)+(1*5)=128
128 % 10 = 8
So 14686-65-8 is a valid CAS Registry Number.
14686-65-8Relevant articles and documents
The Design, Synthesis, and Evaluation of 1,5,7-Trisubstituted-3-Pyridyl-Xanthones for Use as Insecticides Starting from Pyripyropene A
Fuse, Shinichiro,Matsumura, Keisuke,Johmoto, Kohei,Uekusa, Hidehiro,Tanaka, Hiroshi,Hirose, Tomoyasu,Sunazuka, Toshiaki,ōmura, Satoshi,Takahashi, Takashi
, p. 18450 - 18455 (2016)
A readily accessible template of 1,5,7-trisubstituted-3-pyridyl-xanthones was designed starting from naturally occurring pyripyropene A for agrichemical development. Our originally developed Ag2CO3-mediated oxidative cyclization enabled ready access to the key scaffold, 1,5,7-trihydroxy-3-chloro-xanthone. The chemo- and regioselective sequential introduction of four substituents to the scaffold rapidly afforded the desired, structurally diverse 1,5,7-trisubstituted-3-pyridyl-xanthones. An evaluation of insecticidal activity revealed that one of the synthesized compounds retained insecticidal activity against vetch aphid and green peach aphid. The observed insecticidal spectrum was similar to that of pyripyropene A. The developed template could be a valuable aid for future agrichemical development.
A CONVENIENT SYNTHESIS OF NATURALLY OCCURING XANTHONES
Patel, G. N.,Trivedi, K. N.
, p. 1641 - 1648 (2007/10/02)
Six naturally occuring xanthones are synthesized by the thermal condensation of methyl 2,6-dihydroxybenzoate, methyl 2,4-dihydroxybenzoate and methyl 2,4,6-trihydroxybenzoate with hydroquinone, catechol and pyrogallol.
