5580-64-3 Usage
Uses
Used in Laboratory Research and Chemical Synthesis:
(2Z)-2-hydroxyimino-N-naphthalen-2-yl-acetamide is used as a reagent in organic chemistry reactions, contributing to the advancement of scientific knowledge and the development of new chemical compounds.
Used in Pharmaceutical Industry:
Due to its unique chemical properties, (2Z)-2-hydroxyimino-N-naphthalen-2-yl-acetamide may have potential applications in the pharmaceutical industry, possibly leading to the creation of novel drugs or therapeutic agents.
Used in Material Development:
(2Z)-2-hydroxyimino-N-naphthalen-2-yl-acetamide's interesting structural features make it a candidate for the development of new materials, such as polymers or coatings, which could have various industrial and commercial applications.
However, it is crucial to handle (2Z)-2-hydroxyimino-N-naphthalen-2-yl-acetamide with care, as it may pose health and environmental risks if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 5580-64-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,8 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5580-64:
(6*5)+(5*5)+(4*8)+(3*0)+(2*6)+(1*4)=103
103 % 10 = 3
So 5580-64-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H10N2O2/c15-12(8-13-16)14-11-6-5-9-3-1-2-4-10(9)7-11/h1-8,16H,(H,14,15)/b13-8+
5580-64-3Relevant academic research and scientific papers
Potential Antitumor Agents. 61. Structure-Activity Relationships for in Vivo Colon 38 Activity among Disubstituted 9-Oxo-9H-xanthene-4-acetic Acids
Rewcastle, Gordon W.,Atwell, Graham J.,Zhuang, Li,Baguley, Bruce C.,Denny, William A.
, p. 217 - 222 (2007/10/02)
Analogues of 9-oxo-9H-xanthene-4-acetic acid (XAA) bearing small, lipophilic 5-substituents are among the most dose-potent compounds yet reported with the capability of causing hemorrhagic necrosis of implanted colon 38 tumors in mice.To further extend structure-activity relationships among this class of compound, a series of XAA derivatives bearing two small lipophilic groups at various positions have been prepared and evaluated.The 5,6-disubstituted compounds in particular show consistently high levels of both dose potency and activity, suggesting this is the optimal configuration among substituted 9-oxo-9H-xanthene-4-acetic acids.The 5,6-dimethyl and 5-methyl-6-methoxy are the most effective analogues, showing in vivo colon 38 activity comparable to that of FAA at 10-15-fold lower doses and superior activity to FAA at the respective optimal doses, and the former has been selected for detailed evaluation.
