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3H-Pyrrole, 3-diazo-2,4,5-triphenyl- is a chemical compound with the molecular formula C21H15N3. It is a derivative of pyrrole, a heterocyclic aromatic organic compound consisting of a five-membered ring with two carbon atoms and two hydrogen atoms, along with a nitrogen atom. In this specific compound, the pyrrole ring is substituted with three phenyl groups (C6H5) at positions 2, 4, and 5, and a diazo group (-N2) at position 3. 3H-Pyrrole, 3-diazo-2,4,5-triphenyl- is known for its unique chemical properties and potential applications in various fields, such as organic synthesis and materials science. Due to its complex structure and reactivity, it is essential to handle 3H-Pyrrole, 3-diazo-2,4,5-triphenyl- with care and follow proper safety protocols.

2596-88-5

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2596-88-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2596-88-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,9 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2596-88:
(6*2)+(5*5)+(4*9)+(3*6)+(2*8)+(1*8)=115
115 % 10 = 5
So 2596-88-5 is a valid CAS Registry Number.

2596-88-5Relevant academic research and scientific papers

Synthesis and Intramolecular Azo Coupling of 4-Diazopyrrole-2-carboxylates: Selective Approach to Benzo and Hetero [c]-Fused 6H-Pyrrolo[3,4-c]pyridazine-5-carboxylates

Galenko, Ekaterina E.,Galenko, Alexey V.,Khlebnikov, Alexander F.,Novikov, Mikhail S.,Shakirova, Julia R.

, p. 8495 - 8507 (2016/09/28)

A high yield synthesis of fluorescent benzo, thieno, and furo [c]-fused methyl 7-aryl-6H-pyrrolo[3,4-c]pyridazine-5-carboxylates, including unprecedented heterocyclic skeletons, was performed by the transformation of methyl 4-aminopyrrole-2-carboxylate in

3-Diazopyrroles. Part 5 (1). Antibacterial activity of 3-diazo-2-phenylpyrroles

Cirrincione,Almerico,Dattolo,Aiello,Grimaudo,Diana,Misuraca

, p. 1555 - 1562 (2007/10/02)

3-Diazo-2-phenylpyrroles 3a-g showed antimicrobial activity against Gram-positive bacteria, whereas against Gram-negative strains the inhibitory activity is limited to derivatives 3a and 3c. The substituents at 4 and 5 positions strongly influence the inh

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