27525-01-5 Usage
Nitroaromatic compound
It is a type of organic compound that contains a naphthalene ring with a nitro group (-NO2) attached to it.
Cyano and nitro group positions
The cyano group (-CN) is attached at position 1 and the nitro group (-NO2) is attached at position 2 on the naphthalene ring.
Organic synthesis
1-Cyano-2-nitronaphthalene is commonly used as an intermediate in organic synthesis, aiding in the formation of various chemical compounds.
Precursor in chemical production
1-Cyano-2-nitronaphthalene serves as a starting material or building block in the production of other chemicals.
Strong electron-withdrawing properties
The presence of the cyano and nitro groups makes 1-Cyano-2-nitronaphthalene an effective electron-withdrawing agent, which is useful in reactions involving nucleophilic aromatic substitution.
Potential applications in materials science
Researchers have explored the use of 1-Cyano-2-nitronaphthalene as a component in the development of new materials with unique properties.
Building block for functionalized naphthalene derivatives
1-Cyano-2-nitronaphthalene can be used as a starting point for the synthesis of various naphthalene-based derivatives with specific functions or properties.
Toxicity
1-Cyano-2-nitronaphthalene is a toxic compound and can pose health risks if not handled properly. It is essential to follow safety precautions and guidelines when working with this substance.
Check Digit Verification of cas no
The CAS Registry Mumber 27525-01-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,5,2 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 27525-01:
(7*2)+(6*7)+(5*5)+(4*2)+(3*5)+(2*0)+(1*1)=105
105 % 10 = 5
So 27525-01-5 is a valid CAS Registry Number.
27525-01-5Relevant academic research and scientific papers
Studies on Aromatic Nitro Compounds. IV. Reactions of 2-Nitronaphthalenes with Active Methylene Compounds in the Presence of Bases
Tomioka, Yukihiko,Miyake, Junko,Yamazaki, Motoyoshi
, p. 851 - 858 (2007/10/02)
The reactions of 2-nitronaphthalenes with active methylene compounds in the presence of a base were investigated. 2-Nitronaphthalene (I) reacted with ethyl cyanoacetate in the presence of potassium hydroxide to produce ethyl N-(1-cyano-2-naphthyl)oxamate
