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2-(2,5-dichlorophenyl)-1H-pyrrole is an organic compound characterized by its unique molecular structure, which consists of a pyrrole ring fused with a dichlorophenyl group. 2-(2,5-dichlorophenyl)-1H-pyrrole is notable for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a building block for the creation of new molecules with biological activity. The presence of two chlorine atoms on the phenyl ring enhances its reactivity and contributes to its chemical properties, making it a valuable intermediate in organic synthesis. Its chemical formula is C11H7Cl2N, reflecting the presence of 11 carbon atoms, 7 hydrogen atoms, 2 chlorine atoms, and 1 nitrogen atom. The compound's structure and properties make it a subject of interest in the field of organic chemistry, where it is studied for its potential roles in the development of new drugs and chemical compounds.

99113-94-7

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99113-94-7 Usage

Chemical Class

2-(2,5-dichlorophenyl)-1H-pyrrole belongs to the class of pyrrole compounds.

Molecular Weight

206.07 g/mol.

Physical Appearance

White crystalline solid.

Primary Use

Used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and dyes.

Industrial Applications

Serves as a building block in the production of high-performance materials such as polymers and resins.

Health and Environmental Concerns

Identified as a potential endocrine disruptor, banned in some consumer products, and regulated in many countries due to its harmful effects on human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 99113-94-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,1,1 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 99113-94:
(7*9)+(6*9)+(5*1)+(4*1)+(3*3)+(2*9)+(1*4)=157
157 % 10 = 7
So 99113-94-7 is a valid CAS Registry Number.

99113-94-7Downstream Products

99113-94-7Relevant academic research and scientific papers

Arylation of Aromatic Heterocycles with Arenes and Palladium(II) Acetate

Itahara, Toshio

, p. 5272 - 5275 (2007/10/02)

Treatment of aromatic heterocycles such as furfural, 2-acetylfuran, 2-formylthiophene, 2-acetylthiophene, 1-benzoylpyrrole, 1-(2,6-dichlorobenzoyl)pyrrole, 1-acetylindole, and 1-acetyl-3-methylindole with arenes and palladium(II) acetate gave the corresponding aryl-substituted aromatic heterocycles.

Arylation of N-Acyl-pyrroles and -indoles with Arenes and Palladium Acetate

Itahara, Toshio

, p. 254 - 255 (2007/10/02)

Treatment of 1-benzoylpyrroles with palladium acetate in acetic acid containing benzene gave mixtures of 1-benzoyl-2-phenylpyrroles; similar treatment of 1-acetylindoles gave the corresponding 1-acetyl-2-phenylindoles.

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