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1H-Pyrrole-2-carboxaldehyde,3,5-dimethyl-4-nitro-(9CI) is a specific type of chemical compound that falls under the category of organic compounds known as nitropyrrroles. The 1H implies it's a hydrogen-1 isotope, essential for molecular structures. Pyrrole refers to the five-membered aromatic heterocyclic compound, and carboxaldehyde refers to the aldehyde functional group attached to it; it's primarily responsible for giving the compound its chemical properties and reactions. The 3,5-dimethyl part means that there are two methyl groups attached to the third and fifth atoms of the pyrrole ring, while the 4-nitro signifies a nitro functional group connected to the fourth atom.

40236-20-2

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40236-20-2 Usage

Uses

1H-Pyrrole-2-carboxaldehyde,3,5-dimethyl-4-nitro-(9CI) is used as a research compound for [application reason] in the field of organic chemistry.
Used in Research and Laboratory Applications:
1H-Pyrrole-2-carboxaldehyde,3,5-dimethyl-4-nitro-(9CI) is used as a research compound for the study of its chemical properties and potential applications in organic chemistry. 1H-Pyrrole-2-carboxaldehyde,3,5-dimethyl-4-nitro-(9CI) is not known for any significant commercial uses and appears to be largely useful for research or laboratory purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 40236-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,3 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 40236-20:
(7*4)+(6*0)+(5*2)+(4*3)+(3*6)+(2*2)+(1*0)=72
72 % 10 = 2
So 40236-20-2 is a valid CAS Registry Number.

40236-20-2Upstream product

40236-20-2Downstream Products

40236-20-2Relevant academic research and scientific papers

The rearrangement of 3-nitropyridinium salts to 3-nitropyrroles

Glyzdinskaya, Larisa V.,Kuratova, Anna K.,Sagitullina, Galina P.,Vorontsova, Marina A.

, p. 434 - 447 (2017/01/29)

The rearrangement of 3-benzoylamino-5-nitropyridinium quaternary salts by ethanolic methylamine results in the formation of 2-acyl-4-nitropyrroles.

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