57947-01-0

Basic information

• Product Name: 2-amino-N,N-diethylbenzenesulfonamide
• Synonyms: 2-amino-N,N-diethylbenzenesulfonamide;UKRORGSYN-BB BBV-029824;2-aMino-N,N-diethylbenzene-1-sulfonaMide;N,N-Diethyl 2-aMinobenzenesulfonaMide
• CAS NO: 57947-01-0
• Molecular Formula: C₁₀H₁₆N₂O₂S
• Molecular Weight: 228.32
• Mol File: 57947-01-0.mol

Chemical Properties

• Melting Point: 68 °C(Solv: ethanol, 70% (64-17-5))
• Boiling Point: 371.1 °C at 760 mmHg
• Flash Point: 178.2 °C
• Appearance: /
• Density: 1.199 g/cm³
• Vapor Pressure: 1.06E-05mmHg at 25°C
• Refractive Index: 1.56
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 0.28±0.10(Predicted)
• CAS DataBase Reference: 2-amino-N,N-diethylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-N,N-diethylbenzenesulfonamide(57947-01-0)
• EPA Substance Registry System: 2-amino-N,N-diethylbenzenesulfonamide(57947-01-0)

Safety Data

• Hazardous Substances Data: 57947-01-0(Hazardous Substances Data)

Usage

Uses

Used in Pesticide Industry:
2-amino-N,N-diethylbenzenesulfonamide is used as an active ingredient in pesticides for controlling pests and insects in agricultural settings. Its effectiveness in this application is due to its ability to target specific pests while minimizing harm to non-target species and the environment.
Used in Chemical Manufacturing:
2-amino-N,N-diethylbenzenesulfonamide is used as a raw material or intermediate in the synthesis of other chemicals. Its versatile chemical structure allows for the production of a wide range of compounds, making it a valuable component in the chemical industry.
Used in Pharmaceutical Processes:
2-amino-N,N-diethylbenzenesulfonamide is used as a precursor or intermediate in the development of pharmaceutical compounds. Its unique chemical properties enable the creation of new drugs with potential therapeutic applications.
Note: It is important to handle 2-amino-N,N-diethylbenzenesulfonamide with appropriate safety measures due to its potential environmental toxicity. The long-term effects on the environment and health are not well-studied, so caution is advised in its use and disposal.

InChI:InChI=1/C10H16N2O2S/c1-3-12(4-2)15(13,14)10-8-6-5-7-9(10)11/h5-8H,3-4,11H2,1-2H3

Upstream product

• 77925-51-0 2-(N,N-diethylaminosulfonyl)nitrobenzene 
• 1694-92-4 2-Nitrobenzenesulfonyl chloride 
• 119-66-4 2-nitrobenzenediazonium chloride 

Downstream Products

• 77888-52-9 2-(N,N-Diethylaminosulfonyl)benzenesulfonamide 
• 77925-52-1 2-(N,N-diethylsulfamoyl)benzenesulfonyl chloride 

Relevant articles and documents

A simple synthesis of anilines by LiAlH4/TiCl4 reduction of aromatic nitro compounds

A rapid and efficient single-step synthesis of substituted anilines has been developed. The aromatic nitro compounds were reduced by using reducing systems generated by the action of an excess of LiAlH4 on TiCl4. Anilines substituted with different functional groups were synthesized in high yields and purity starting from the corresponding nitro compounds. The developed procedure is applicable to nitroaromatics containing both electron withdrawing and electron donating substituents. Substrates with electron donor substituents require a larger excess of LiAlH4. The reducing power of the prepared reactant systems depends on the used molar ratio of LiAlH4 and TiCl4.

Azo coupling of o- and p-(dialkylaminosulfonyl)benzene-diazonium salts with 7-acetylamino-4-hydroxynaphthalene-2-sulfonic acid in citrate-phosphate buffer solution

Dependences of the partial rate constants for azo coupling of o-(dialkylaminosulfonyl)benzene-diazonium salts with 7-acetylamino-4-hydroxynaphthalene-2-sulfonic acid (N-Acetyl-I-acid) on the fraction of the dianionic form of the latter indicate considerable steric hindrances to the second stage of the reaction. Ionization of the hydroxy group of N-acetyl-I-acid gives rise to additional electrostatic repulsion at the stage of formation of the σ complex, which reduces the rate of azo coupling at the 3-position of orthanilic acid.

Herbicidal N-(pyridinylaminocarbonyl)benzenesulfonamides

N-(Pyridinylaminocarbonyl)benzenesulfonamides are useful for the regulation of plant growth and as pre-emergence and post-emergence herbicides.

N(Substituted phenylsulfonyl) N'(substituted cyumidin-2-yl) ureas

This invention relates to N(Substituted Phenylsulfonyl) N'(Substituted Pyrimidinyl) urea compounds having the formulae I and IA STR1 to agricultural compositions containing them and to their methods of use as general as well as selective pre- and post-eme

Herbicidal N-(pyridinylaminocarbonyl)benzenesulfonamides

N-(Pyridinylaminocarbonyl)benzenesulfonamides are useful for the regulation of plant growth and as pre-emergence and post-emergence herbicides.