897-16-5 Usage
Description
(2E)-[(4E)-4-(hydroxyimino)cyclohexa-2,5-dien-1-ylidene](naphthalen-1-yl)ethanenitrile is a complex organic molecule with a 3D structure, featuring a naphthalene ring connected to a hydroxyimino-cyclohexa-2,5-dien-1-ylidene group and an ethanenitrile group. As a derivative of naphthalene, this compound holds potential applications across various fields, including pharmaceuticals, agrochemicals, and material science. Further analysis and research are necessary to explore its specific properties and uses.
Uses
Used in Pharmaceutical Industry:
(2E)-[(4E)-4-(hydroxyimino)cyclohexa-2,5-dien-1-ylidene](naphthalen-1-yl)ethanenitrile is used as a potential pharmaceutical agent for its unique molecular structure, which may offer novel therapeutic properties and interactions with biological targets.
Used in Agrochemical Industry:
In the agrochemical sector, (2E)-[(4E)-4-(hydroxyimino)cyclohexa-2,5-dien-1-ylidene](naphthalen-1-yl)ethanenitrile is utilized as a component in the development of new pesticides or herbicides, leveraging its chemical properties to control or eliminate unwanted plant species.
Used in Material Science:
(2E)-[(4E)-4-(hydroxyimino)cyclohexa-2,5-dien-1-ylidene](naphthalen-1-yl)ethanenitrile serves as a building block in material science for the synthesis of advanced materials with specific properties, such as improved conductivity, stability, or reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 897-16-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,9 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 897-16:
(5*8)+(4*9)+(3*7)+(2*1)+(1*6)=105
105 % 10 = 5
So 897-16-5 is a valid CAS Registry Number.
897-16-5Relevant articles and documents
Antitumor chemotherapy. XIV. Cytotoxic activity of compounds possessing an ethylenic double bond substituted at the α and β positions with an electron attracting group
Dore Ch.,Viel
, p. 47 - 54 (2007/10/04)
The authors have previously shown that molecules possessing an ethylene double bond, activated by one or 2 electron attracting substituents, show a cytotoxic activity which must be connected with the addition of a cellular nucleophil to their double bond. This correlation has been extended to N alkylmaleinimides and different compounds with paraquinonine structure. The compounds examined possess a distinct cytotoxic antitumor activity which is, however, inferior to that of α nitro stilbenes and β nitro styrenes, the simplified analogs of aristolochic acid.
