2672-77-7 Usage
Description
N-(2,4-dimethoxyphenyl)-3-hydroxynaphthalene-2-carboxamide is a chemical compound that belongs to the class of carboxamides. It features a naphthalene core with a carboxamide group and a hydroxyl group, as well as a 2,4-dimethoxyphenyl substituent. This molecular structure and its functional groups suggest potential interactions with various biological targets and pathways, indicating its potential as a candidate for drug development and therapeutic applications.
Uses
Used in Pharmaceutical Industry:
N-(2,4-dimethoxyphenyl)-3-hydroxynaphthalene-2-carboxamide is used as a pharmaceutical agent for its potential biological and pharmacological activities. It is known for its anti-inflammatory, analgesic, and antipyretic properties, which can be beneficial in the treatment of various conditions that involve inflammation, pain, and fever.
Used in Drug Development:
Due to its potential interactions with biological targets and pathways, N-(2,4-dimethoxyphenyl)-3-hydroxynaphthalene-2-carboxamide is used in drug development to explore its therapeutic applications further. This may involve designing and testing new drugs based on its molecular structure and properties to treat specific diseases or conditions.
Further research and studies are needed to fully understand and explore the biological activities and potential uses of N-(2,4-dimethoxyphenyl)-3-hydroxynaphthalene-2-carboxamide, ensuring its safety and efficacy in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 2672-77-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,7 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2672-77:
(6*2)+(5*6)+(4*7)+(3*2)+(2*7)+(1*7)=97
97 % 10 = 7
So 2672-77-7 is a valid CAS Registry Number.
InChI:InChI=1/C19H17NO4/c1-23-14-7-8-16(18(11-14)24-2)20-19(22)15-9-12-5-3-4-6-13(12)10-17(15)21/h3-11,21H,1-2H3,(H,20,22)
2672-77-7Relevant articles and documents
Fluorescent substrates for potential use in enzyme-linked immunosorbent assay of membrane-bound nucleic acids
Fujita, Satoshi,Momiyama, Masayoshi,Kondo, Yasumitsu,Kagiyama, Naoto,Hori, Samuel H.,Toru, Takeshi
, p. 1347 - 1353 (2007/10/02)
A number of phosphorylated fluorochromes were synthesized and tested for the alkaline phosphatase-linked fluorescence assay of membrane-bound nucleic acids. 3-Hydroxy-N-2′-biphenyl-2-naphthalenecarboxamide phosphate ester (HBNP) was found to be the most suitable for the assay. Nonfluorescent HBNP is hydrolyzed by phospholipase bound to the probe DNA to the highly fluorescent 3-hydroxy-N,2′-biphenyl-2-naphthalenecarboxamide (HBN). HBN is insoluble enough in aqueous medium to precipitate on the nylon membrane. Spots containing as little as 5 fg of λ DNA can be successfully detected on the membrane with HBNP.
