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AgrochemicalsChlorsulfuron Impurity 1

SKU: SAC-13-A

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Name:1-Chloro-4-[(4-methoxybenzyl)oxy]-2-nitrobenzene CAT. NO.:SAC-13-A CAS NO.:236111-74-3

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  • Datasheet
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Description

Chlorsulfuron Impurity 1

Chemical Name 1-Chloro-4-[(4-methoxybenzyl)oxy]-2-nitrobenzene
Catalog Number SAC-13-A
Parent AI Chlorsulfuron
Synonyms 1-Chloro-4-[(4-methoxyphenyl)methoxy]-2-nitrobenzene
CAS Number 236111-74-3
Molecular Formula C₁₄H₁₂ClNO₄
Molecular Weight 293.7
Appearance Pale yellow solid
Melting Point NA
Shipping & Storage Information

 

Storage 20°C

Shipping: Free Shipping at Room Temperature in INDIA,  may vary elsewhere

Stability: Datasheet

Solubility Dichloromethane
Stability Stable under recommended storage conditions
Category Standards; Pharmaceutical/API Drug Impurities/Metabolites
Description &Applications 1-Chloro-4-[(4-methoxybenzyl)oxy]-2-nitrobenzene is an intermediates in the synthesis of 5-hydroxy Chlorosulfuron (H839405) which is a derivative of Chlorosulfuron(C384978). Chlorsulfuron blocks the biosynthesis of valine [72-​18-​4] and isoleucine [73-​32-​5] in plants.
References Thomas, R.: Plant Physiol., 75, 827 (1984)

1-Chloro-4-[(4-methoxybenzyl)oxy]-2-nitrobenzene, often abbreviated as CMBONB, is a chemically intriguing compound with significant applications in various fields. This aromatic organic compound belongs to the class of nitrobenzenes, characterized by the presence of a nitro group (-NO2) on a benzene ring. The compound’s unique structure and versatile reactivity have led to its use in pharmaceuticals, agrochemicals, and materials science.

Synthesis: The synthesis of 1-Chloro-4-[(4-methoxybenzyl)oxy]-2-nitrobenzene involves several steps of chemical transformation. One common approach to its synthesis is through the reaction of 4-hydroxy-1-methoxybenzene (p-anisole) with p-chloronitrobenzene in the presence of suitable catalysts and reagents. The reaction includes protection of the hydroxyl group, followed by chlorination and nitration steps to yield the final product.

Properties: 1-Chloro-4-[(4-methoxybenzyl)oxy]-2-nitrobenzene possesses several noteworthy properties:

  1. Aromatic Nature: The compound features an aromatic benzene ring, which contributes to its stability and reactivity patterns.
  2. Functional Groups: The presence of a chlorine atom, a methoxy group (-OCH3), and a nitro group (-NO2) introduces diverse reactivity sites that can be harnessed for various chemical transformations.
  3. Solubility: CMBONB exhibits solubility in organic solvents like dichloromethane, acetone, and ethyl acetate. This property aids in its manipulation and application in various reactions.
  4. Melting Point: The melting point of this compound falls within a specific range, allowing for its identification and characterization.

Applications:

  1. Pharmaceuticals: CMBONB and its derivatives have demonstrated potential in medicinal chemistry. They can serve as intermediates in the synthesis of biologically active compounds, including pharmaceuticals used to treat various medical conditions.
  2. Agrochemicals: The compound’s reactivity and functional groups make it useful in the synthesis of agrochemicals such as pesticides and herbicides. These compounds play a crucial role in modern agriculture by protecting crops from pests and enhancing yield.
  3. Materials Science: The aromatic nature of CMBONB renders it valuable in materials science applications. It can be used as a precursor in the creation of polymers, dyes, and other specialty chemicals used in the production of advanced materials.
  4. Research and Development: The unique structural features of this compound make it an interesting target for researchers exploring new synthetic methods and reaction pathways. Its participation in diverse chemical transformations contributes to the advancement of chemical science.

Additional information

Pack Size

50mg

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