4779-36-6

Basic information

• Product Name: 1-Chloro-2-nitro-4-(phenylsulfonyl)benzene
• Synonyms: 1-Chloro-2-nitro-4-(phenylsulfonyl)benzene;Benzene, 1-chloro-2-nitro-4-(phenylsulfonyl)-
• CAS NO: 4779-36-6
• Molecular Formula: C₁₂H₈ClNO₄S
• Molecular Weight: 298
• Mol File: 4779-36-6.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-Chloro-2-nitro-4-(phenylsulfonyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Chloro-2-nitro-4-(phenylsulfonyl)benzene(4779-36-6)
• EPA Substance Registry System: 1-Chloro-2-nitro-4-(phenylsulfonyl)benzene(4779-36-6)

Safety Data

• Hazardous Substances Data: 4779-36-6(Hazardous Substances Data)

Usage

General Description

1-Chloro-2-nitro-4-(phenylsulfonyl)benzene is a chemical compound with the molecular formula C12H8ClNO4S. It is a nitrochlorobenzene derivative with a phenylsulfonyl group attached to the 4-position. 1-Chloro-2-nitro-4-(phenylsulfonyl)benzene is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is also used as a reagent in organic synthesis, particularly in the production of biologically active compounds. The presence of the nitro group in this compound makes it a valuable building block for the synthesis of diverse aromatic compounds. Additionally, the chloro and sulfonyl groups make it a versatile compound for the introduction of functional groups in organic synthesis. Overall, 1-Chloro-2-nitro-4-(phenylsulfonyl)benzene has several applications in the field of organic chemistry and is an important intermediate in the production of various chemical compounds.

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Relevant articles and documents

Manufacturing method of piperidinyl sulfonyl sulfonamide

The present invention relates to the preparation of diphenylsulfonylamide represented by formula 1. Chemically 1 _AOMARKENCODEGTX06017. A compound represented by chemical formula 2 is obtained by reacting a compound represented by chemical formula 3 with N-protected piperidine amine to obtain a compound represented by the following formula, wherein N is protected with N-protected piperidine amine to obtain a compound represented by chemical formula 4 6, and to obtain a compound represented by the 6 7 formula 5 of the compound represented by the following general formula in the following 7 chemical formula 5 to obtain a compound represented by the following general formula (1 I). AOMARKENCODELTX017. Chemically 2 _AOMARKENCODEGTX06017. AOMARKENCODELTX017. Chemically 3 _AOMARKENCODEGTX06017. AOMARKENCODELTX017. Chemically 4 _AOMARKENCODEGTX06017. AOMARKENCODELTX017. Chemically 5 _AOMARKENCODEGTX06017. AOMARKENCODELTX017. Chemically 6 _AOMARKENCODEGTX06017. AOMARKENCODELTX017. Chemically 7 _AOMARKENCODEGTX06017.

Modulation of Wnt signaling through inhibition of secreted frizzled-related protein i (sFRP-1) with N-substituted piperidinyl diphenylsulfonyl sulfonamides

The diphenylsulfonyl sulfonamide scaffold represented by 1 (WAY-316606) are small molecule inhibitors of the secreted protein sFRP-1, an endogenous antagonist of the secreted glycoprotein Wnt. Modulators of the Wnt pathway have been proposed as anabolic a

2H-Benzimidazoles (Isobenzimidazoles). Part 3. Thermal Isomerisation of Substituted 2H-Benzimidazoles to 1H-Benzimidazoles

2H-Benzimidazole-2-spirocyclohexanes (1) when heated undergo a 1,5-sigmatropic rearrangement to 2,3-disubstituted 1H-benzimidazoles.A decided effect on the direction of this isomerisation was observed with substituents in the homodiene ring.