Name: Butachlor Impurity 3 - SRIRAMCHEM
SKU: SAB-15-C
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Butachlor Impurity 3, 2-chloro-N-(2,6-diethylphenyl)acetamide, 6967-29-9

AgrochemicalsButachlor Impurity 3

SKU: SAB-15-C

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

Name:2-chloro-N-(2,6-diethylphenyl)acetamide

CAT. NO.:SAB-15-C

CAS NO.:6967-29-9

Description
Datasheet
Additional information

Description

Butachlor Impurity 3

Chemical Name	2-chloro-N-(2,6-diethylphenyl)acetamide
Catalog Number	SAB-15-C
Parent AI	Butachlor
Synonyms	2-Chloro-2′,6′-diethylacetanilide; 2′,6′-Diethyl-2-chloroacetanilide; 2′,6′-Diethylchloroacetanilide; N-(2,6-Diethylphenyl)-2-chloroacetamide; N-(2,6-Diethylphenyl)chloroacetamide; NSC 68291;ω-Chloro-2′,6′-diethylacetanilide
CAS Number	6967-29-9
Molecular Formula	C₁₂H₁₆ClNO
Molecular Weight	225.71
Appearance	White to Off-White Solid
Melting Point	135-136°C
Shipping & Storage Information	Storage-20°C, , Inert atmosphere Shipping: Free Shipping at Room Temperature in INDIA, may vary elsewhere Stability: Datasheet
Solubility	DMSO (Slightly), Methanol (Slightly)
Stability	Moisture Sensitive
Category	Agrochemical Impurity Standard/Metabolites
Description &Applications	It is also known as 2-CNDP, is a synthetic organic compound with a wide range of applications in the fields of science and engineering. 2-CNDP is an important intermediate in the synthesis of many organic compounds and is used as a catalyst in various chemical reactions. The compound has been studied extensively for its potential use in the treatment of various diseases and disorders, including cancer, diabetes, and neurological disorders
References	Zhang, M. et al.: Eur. J. Med. Chem., 62, 301 (2013)

The synthesis of 2-Chloro-N-(2,6-diethylphenyl)acetamide involves several steps of organic chemical reactions. One common method to synthesize this compound is by starting with 2,6-diethylphenylamine, which undergoes a reaction with chloroacetyl chloride. This reaction forms the amide bond and introduces the chlorine atom. Careful control of reaction conditions and purification steps is essential to achieve a high yield of the desired compound.

Applications:

Medicinal Chemistry: Compounds containing amide groups often exhibit interesting biological activities. Researchers explore the potential of 2-Chloro-N-(2,6-diethylphenyl)acetamide and its derivatives as pharmaceutical agents. They might act as antibacterial, antifungal, or even anticancer agents due to their ability to interact with biological macromolecules.
Agrochemicals: The diverse properties of this compound can make it a suitable candidate for the development of agrochemicals. It might serve as a key component in new pesticide formulations or plant growth regulators, contributing to sustainable agriculture practices.
Material Science: The unique structure of the compound lends itself to modification for various material science applications. It could be incorporated into polymers, coatings, or functional materials, enhancing their properties and performance.
Intermediates in Synthesis: 2-Chloro-N-(2,6-diethylphenyl)acetamide can also serve as a valuable intermediate in the synthesis of more complex compounds. By utilizing its specific reactivity, chemists can create compounds with tailored functionalities.

Challenges and Considerations: While 2-Chloro-N-(2,6-diethylphenyl)acetamide shows promise across multiple applications, its successful utilization requires addressing challenges related to synthesis scalability, compound stability, and toxicity assessments. Researchers must also consider eco-friendly and sustainable methods for synthesis and application.