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AgrochemicalsCarbofuran Impurity 6

SKU: SAC-05-F

Original price was: ₹60,000.00.Current price is: ₹50,000.00.

Name:2,3-Dihydro-2,2-dimethyl-7-nitrobenzofuran CAT. NO.:SAC-05-F CAS NO.:13414-55-6

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  • Datasheet
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Description

Carbofuran Impurity 6

Chemical Name 2,3-Dihydro-2,2-dimethyl-7-nitrobenzofuran
Catalog Number SAC-05-F
Parent AI Carbofuran
Synonyms 2,2-Dimethyl-7-nitro-2,3-dihydro-1-benzofuran
CAS Number 13414-55-6
Molecular Formula C₁₀H₁₁NO₃
Molecular Weight 193.2
Appearance colorless, crystalline solid
Melting Point 65-67 °C
Shipping & Storage Information

 

Storage-20°C

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

Stability: Datasheet

Solubility NA
Stability Stable under recommended storage conditions
Category Standards; Environmental Standards, Mutagens and Metabolites; Pesticides
Description &Applications 2,3-Dihydro-2,2-dimethyl-7-nitrobenzofuran is an impurity of Carbofuran (C176590), which is a a cholinesterase inhibitor. Also used as systemic insecticide, acaricide, and nematocide. Used in Pesticide detection.
References Dorough, W.H., et al.: J. Agric. Food Chem., 16, 319 (1968)

“2,3-Dihydro-2,2-dimethyl-7-nitrobenzofuran,” a mouthful of a name that hints at the compound’s complex structure and potential significance. This article delves into the world of 2,3-Dihydro-2,2-dimethyl-7-nitrobenzofuran, exploring its structure, synthesis, properties, and possible applications.

Structure and Composition: At first glance, the name might appear daunting, but breaking it down reveals key insights. “2,3-Dihydro” indicates the presence of two hydrogen atoms at positions 2 and 3 on the molecule’s carbon backbone. “2,2-dimethyl” signifies the attachment of two methyl groups (CH3) at the same carbon atom, adding steric bulkiness. “7-nitro” highlights the presence of a nitro group (NO2) at position 7, which consists of a nitrogen atom bonded to two oxygen atoms. Lastly, “benzofuran” describes a fused ring system consisting of a benzene ring fused with a furan ring.

Synthesis: The synthesis of 2,3-Dihydro-2,2-dimethyl-7-nitrobenzofuran is a carefully orchestrated process that involves several chemical reactions. One common method involves the nitration of 2,2-dimethyl-3,4-dihydrobenzofuran, where the nitro group is introduced using nitric acid and sulfuric acid. The resulting compound is then reduced to obtain the desired product – 2,3-Dihydro-2,2-dimethyl-7-nitrobenzofuran. This synthesis route showcases the delicate balance between functional group transformations and ring formation.

Properties: The compound’s intricate structure directly influences its properties. The fused benzene-furan ring imparts aromatic characteristics, making the molecule electronically interesting. The nitro group introduces polarity and electron-withdrawing effects, affecting the compound’s reactivity. The steric hindrance due to the methyl groups affects interactions with other molecules. These properties collectively influence its behavior in various chemical reactions and potential applications.

Potential Applications: While specific applications of 2,3-Dihydro-2,2-dimethyl-7-nitrobenzofuran might not be extensively documented, its unique structural features suggest possible roles in diverse areas of chemistry:

  1. Medicinal Chemistry: The compound’s aromatic and nitro group functionalities could render it valuable for designing molecules with potential pharmaceutical activity. Nitro groups are known to participate in various biological processes.
  2. Materials Science: Aromatic compounds often find applications in the development of advanced materials due to their electronic properties. This compound might contribute to the creation of novel materials with tailored electronic characteristics.
  3. Synthetic Chemistry: Its complex structure challenges synthetic chemists to explore creative methodologies for its preparation. Developing efficient synthesis routes can have broader implications for the field.
  4. Biological Activity: The compound’s unique structure might lead to interesting biological interactions, making it a subject of interest in studying enzyme-substrate interactions and other biochemical processes.
  5. Chemical Research: Even if not directly applied, compounds like these inspire researchers to investigate new reaction mechanisms and explore uncharted territories in organic chemistry.

Additional information

Pack Size

50mg

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