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1-(4-bromophenyl)-1H-pyrrole-2-carbaldehyde, also known as 4-Bromo-α-pyrrol-2-yl-benzaldehyde, is a chemical compound characterized by its molecular formula C11H8BrNO. This yellow solid has a molecular weight of 246.09 g/mol and is an aldehyde derivative of pyrrole, a five-membered aromatic heterocyclic molecule. It is recognized for its role as a building block in the synthesis of various pharmaceutical and biologically active compounds. Its potential applications in organic synthesis, material science, and its bioactive properties make it a subject of interest for researchers in medicinal chemistry and drug discovery.

30186-40-4

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30186-40-4 Usage

Uses

Used in Pharmaceutical and Biologically Active Compounds Synthesis:
1-(4-bromophenyl)-1H-pyrrole-2-carbaldehyde is used as a key building block for the synthesis of pharmaceutical and biologically active compounds. Its unique structure and reactivity contribute to the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(4-bromophenyl)-1H-pyrrole-2-carbaldehyde is used as a versatile intermediate for creating a wide range of chemical products. Its aldehyde group allows for various reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Material Science:
1-(4-bromophenyl)-1H-pyrrole-2-carbaldehyde is also utilized in material science, where its properties can be harnessed to develop new materials with specific characteristics. Its potential applications in this field are still being explored, but it holds promise for contributing to advancements in material technology.
Used in Medicinal Chemistry and Drug Discovery:
As a compound with bioactive properties, 1-(4-bromophenyl)-1H-pyrrole-2-carbaldehyde is used in the field of medicinal chemistry and drug discovery. Researchers employ 1-(4-bromophenyl)-1H-pyrrole-2-carbaldehyde to investigate its potential therapeutic effects and to design new drugs targeting various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 30186-40-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,1,8 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 30186-40:
(7*3)+(6*0)+(5*1)+(4*8)+(3*6)+(2*4)+(1*0)=84
84 % 10 = 4
So 30186-40-4 is a valid CAS Registry Number.

30186-40-4Downstream Products

30186-40-4Relevant academic research and scientific papers

SYNTHESIS AND SPECTRAL PROPERTIES OF 1-ARYL-2-FORMYLPYRROLES

Pina, M. del' K.,Budylin, V. A.,Rodriges, M.,Terent'ev, P. B.,Bundel', Yu. G.

, p. 142 - 146 (2007/10/02)

Various 1-aryl-2-formylpyrroles were synthesized by reaction of furfurol with substituted anilines.For p-bromo- and p-chlorophenyl substituents, the intermediate Schiff bases were isolated.

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