93493-69-7 Usage
Description
1,7-Naphthyridine, 2,6-dichlorois a chemical compound belonging to the naphthyridine family, characterized by the molecular formula C10H5Cl2N. It features a naphthyridine ring with two chlorine atoms attached at the 2 and 6 positions, endowing it with diverse biological activities and potential medicinal properties.
Uses
Used in Pharmaceutical Development:
1,7-Naphthyridine, 2,6-dichloroserves as a valuable intermediate in the development of various pharmaceuticals due to its antitumor, antibacterial, and antifungal properties. It plays a crucial role in the synthesis of drugs targeting a range of health conditions.
Used in Agrochemical Development:
1,7-NAPHTHYRIDINE, 2,6-DICHLOROalso finds application in the agrochemical industry, where it is utilized in the development of products with antitumor, antibacterial, and antifungal properties, contributing to enhanced crop protection and management.
Used as a Fluorescent Probe in Analytical Chemistry:
1,7-Naphthyridine, 2,6-dichlorohas been investigated for its potential use as a fluorescent probe for detecting metal ions, which can be beneficial in various analytical and environmental applications.
Used in the Development of Advanced Materials:
Furthermore, this compound has been explored for its role in the development of new materials with optical and electronic properties, indicating its potential use in high-tech industries and research.
Check Digit Verification of cas no
The CAS Registry Mumber 93493-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,4,9 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 93493-69:
(7*9)+(6*3)+(5*4)+(4*9)+(3*3)+(2*6)+(1*9)=167
167 % 10 = 7
So 93493-69-7 is a valid CAS Registry Number.
93493-69-7Relevant articles and documents
Naphthyridinyloxy(or thio)phenoxy propanoic acids, derivatives thereof and methods of herbicidal use
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, (2008/06/13)
Novel 2-naphthyridinyloxy(or thio)phenoxy propanoic acid compounds of the formula STR1 wherein STR2 represents a 6 membered nitrogen containing an aromatic ring which forms a 1,5-, 1,6-, 1,7- or 1,8-naphthyridinyl moiety with the adjoining pyridine ring,
