99902-78-0 Usage
Molecular Weight
330.11 g/mol
Structure
The molecule consists of a benzene ring with a nitro group (-NO2) at the 5-position, a nitrile group (-C≡N) attached to the 2-position, and a bromophenoxy group (-C6H4BrO) attached to the 2-position.
+ Appearance
Yellow crystalline solid
+ Melting Point
94-96°C
+ Solubility
Slightly soluble in water, soluble in common organic solvents such as ethanol, methanol, and acetone.
+ Reactivity
The presence of the nitro group and the nitrile group makes the molecule highly reactive and susceptible to various chemical reactions, such as reduction, hydrolysis, and condensation.
+ Bromophenoxy group
The presence of the bromophenoxy group adds to the reactivity of the molecule and allows for further functionalization and derivatization.
+ Building block
2-(2-bromophenoxy)-5-nitrobenzonitrile is used as a building block in the synthesis of various pharmaceuticals and agrochemicals.
+ Organic synthesis
The compound has potential applications in the field of organic synthesis due to its reactivity and functional groups.
+ Medicinal chemistry
The compound is also important for research and development in medicinal chemistry, as it can be used to synthesize biologically active molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 99902-78-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,9,0 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 99902-78:
(7*9)+(6*9)+(5*9)+(4*0)+(3*2)+(2*7)+(1*8)=190
190 % 10 = 0
So 99902-78-0 is a valid CAS Registry Number.
99902-78-0Relevant articles and documents
Synthesis and anti-CVB 3 evaluation of substituted 5-nitro-2-phenoxybenzonitriles
Puerstinger, Gerhard,De Palma, Armando M.,Zimmerhofer, Guenther,Huber, Simone,Ladurner, Sophie,Neyts, Johan
experimental part, p. 5123 - 5125 (2009/04/16)
The synthesis and SAR of a series of 60 substituted 2-phenoxy-5-nitrobenzonitriles (analogues of MDL-860) as inhibitors of enterovirus replication (in particular of coxsackievirus B3 (CVB 3)) are reported. Several of the analogues inhibited CVB 3 and othe
