53820-85-2 Usage
Properties & Specific Content of 1H-inden-3-yl 4-nitrobenzoate
A compound with 20 carbon atoms, 13 hydrogen atoms, 1 nitrogen atom, and 4 oxygen atoms in its molecular structure.
Derivation
1H-inden-3-yl and 4-nitrobenzoic acid
1H-inden-3-yl 4-nitrobenzoate is synthesized by combining a fused bicyclic aromatic hydrocarbon (1H-inden-3-yl) with a derivative of benzoic acid (4-nitrobenzoic acid).
Bicyclic Structure
Fused bicyclic aromatic hydrocarbon
The 1H-inden-3-yl component features a bicyclic (two interconnected rings) structure with aromatic properties (stability and delocalization of electrons).
Nitro Group
Substituted at the para position
A nitro group (-NO2) is attached to the 4-nitrobenzoate moiety at the para position (opposite side of the benzene ring), which contributes to the compound's reactivity and potential applications.
Industrial Applications
Pharmaceutical, agrochemical, and materials science industries
The presence of the nitro group makes 1H-inden-3-yl 4-nitrobenzoate a valuable compound for various applications in pharmaceuticals, agrochemicals, and materials science due to its reactivity and versatility.
Synthesis Intermediate
Organic synthesis and functional materials preparation
1H-inden-3-yl 4-nitrobenzoate can serve as a valuable intermediate for the synthesis of other organic compounds with diverse industrial and academic applications, such as the preparation of functional materials.
Check Digit Verification of cas no
The CAS Registry Mumber 53820-85-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,2 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53820-85:
(7*5)+(6*3)+(5*8)+(4*2)+(3*0)+(2*8)+(1*5)=122
122 % 10 = 2
So 53820-85-2 is a valid CAS Registry Number.
