96090-15-2 Usage
Chemical compound
2-(3,4-Diethoxyphenyl)-3-nitro-2H-chromene is a chemical compound consisting of a nitro group and a chromene ring structure.
Common uses
It is commonly used in organic synthesis and pharmaceutical research due to its potential biological activities.
Biological activities
Nitrochromene has been studied for its anti-inflammatory, anti-cancer, and anti-microbial properties, making it a promising candidate for drug development.
Molecular structure
Its unique molecular structure allows for the modification of its functional groups, which can lead to the development of new compounds with improved pharmacological properties.
Check Digit Verification of cas no
The CAS Registry Mumber 96090-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,0,9 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 96090-15:
(7*9)+(6*6)+(5*0)+(4*9)+(3*0)+(2*1)+(1*5)=142
142 % 10 = 2
So 96090-15-2 is a valid CAS Registry Number.
96090-15-2Relevant academic research and scientific papers
THE SYNTHESIS OF 2-PHENYL-3-NITRO-3,4-DIHYDRO-2H-1-BENZOPYRANS
Varma, Rajender S.,Kadkhodayan, Miryam,Kabalka, George W.
, p. 1647 - 1652 (2007/10/02)
A series of 3-nitrochromans, including a 3-phenyl-2-nitrodihydronaphthopyran, were synthesized in good yields by selective reduction of the corresponding 3-nitrochromenes using sodium borohydride in methanolic tetrahydrofuran.
A convenient one-pot synthesis of 3-nitro-2H-chromenes by ultrasonic agitation on basic alumina
Varma, Rajender S.,Kabalka, George W.
, p. 139 - 141 (2007/10/02)
The condensation of o-hydroxybenzaldehyde with β-nitrostyrene derivatives was carried out on basic alumina.Sonic acceleration of this condensation provides a convenient synthesis of 2-phenyl-3-nitro-2H-1-benzopyrans in good yields
