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N-(1-anthracenyl)-4-nitrobenzaldimine is an organic compound characterized by its unique molecular structure, which consists of an anthracene moiety attached to a nitrobenzene group through an imine bond. N-(1-anthracenyl)-4-nitrobenzaldimine is known for its distinct fluorescence properties, making it a potential candidate for applications in the field of chemosensing and as a fluorophore in various analytical techniques. The presence of the nitro group on the benzene ring introduces electron-withdrawing characteristics, which can significantly influence the compound's reactivity and stability. Its chemical formula is C21H13N3O2, and it is often used in research to study molecular interactions and the effects of structural modifications on optical properties.

905-87-3

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905-87-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 905-87-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,0 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 905-87:
(5*9)+(4*0)+(3*5)+(2*8)+(1*7)=83
83 % 10 = 3
So 905-87-3 is a valid CAS Registry Number.

905-87-3Relevant academic research and scientific papers

Solvent-free one pot synthesis of indenoquinolinones catalyzed by iron(III) trifl ate

Damavandi, Saman,Sandaroos, Reza

, p. 121 - 124 (2011)

A green three-component one pot condensation synthesis of 16 indenoquinolinone from aromatic aldehydes, 1-aminonaphthalene or 1-aminoanthracene and 1,3-indanedione catalyzed by Fe(OTf)3 is described. The isolated yields ranged from 80 % to 92 %

Efficient example of cross-linked polymeric catalysed synthesis of 7H-benzo[h]indeno[1,2-b]quinolin-8-one and 8H-naphtho[2,3-h]indeno[1,2-b] quinolin-9-one

Sandaroos, Reza,Vadi, Mehdi,Damavandi, Saman

, p. 1497 - 1501 (2014/04/03)

Cross-linked poly(2-acrylamido-2-methyl propane sulphonic acid) (AMPS) was found to be an efficient heterogeneous catalyst for direct synthesis of 7H-benzo[h]indeno[1, 2-b]quinolin-8-one and 8Hnaphtho[ 2, 3-h]indeno[1, 2-b]quinolin-9-one derivatives throu

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