10372-41-5

Basic information

• Product Name: 3-AMINO-N,N-DIETHYL-BENZENESULFONAMIDE
• Synonyms: N,N-DIETHYL 3-AMINOBENZENESULFONAMIDE;3-AMINO-N,N-DIETHYL-BENZENESULFONAMIDE;3-AMINO-N,N-DIMETHYLBENZENESULFONAMIDE
• CAS NO: 10372-41-5
• Molecular Formula: C₁₀H₁₆N₂O₂S
• Molecular Weight: 228.31
• Product Categories: blocks;Sulfonamides;Amines
• Mol File: 10372-41-5.mol

Chemical Properties

• Boiling Point: 388.4 °C at 760 mmHg
• Flash Point: 188.7 °C
• Appearance: /
• Density: 1.199 g/cm³
• Vapor Pressure: 3.08E-06mmHg at 25°C
• Refractive Index: 1.56
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• CAS DataBase Reference: 3-AMINO-N,N-DIETHYL-BENZENESULFONAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-AMINO-N,N-DIETHYL-BENZENESULFONAMIDE(10372-41-5)
• EPA Substance Registry System: 3-AMINO-N,N-DIETHYL-BENZENESULFONAMIDE(10372-41-5)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 10372-41-5(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
3-AMINO-N,N-DIETHYL-BENZENESULFONAMIDE is used as an active pharmaceutical ingredient for its anticonvulsant activity, particularly in the treatment of epileptic conditions. It helps in managing seizures and reducing the frequency of epileptic episodes by modulating the neuronal activity in the brain.
Used in Research and Development:
3-AMINO-N,N-DIETHYL-BENZENESULFONAMIDE serves as a valuable research intermediate in the development of new drugs and therapies. Its unique chemical structure allows scientists to explore its potential in various applications, such as the synthesis of novel anticonvulsant drugs, and the study of its interactions with other molecules and biological systems.

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

Upstream product

• 6335-26-8 3-nitro-benzenesulfonic acid diethylamide 
• 109-89-7 diethylamine 
• 121-51-7 3-nitrobenzenesulphonyl chloride 

Downstream Products

• 1622393-03-6 C₁₇H₂₀N₂O₃S₂ 
• 565165-15-3 C₁₇H₁₈N₂O₃S₂ 
• 1038740-94-1 C₁₆H₂₂N₄O₃S 
• 188263-57-2 6-tert-Butyl-8-isocyanato-4-oxo-4H-chromene-2-carboxylic acid (3-diethylsulfamoyl-phenyl)-amide 

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.

Herbicidally active phenoxyalkanecarboxylic acid derivatives

A compound of the formula: STR1 wherein Q1 is CH or N; R is H or C1 -C5 alkyl; X is H, halogen, CF3, or NO2 ; Y is H or halogen; Z is --O-- or --NH--; A is STR2 wherein Q2, and Q3 are each CH or N; R1 and R2 are each H, C1 -C5 alkyl, C1 -C5 alkoxy, or C2 -C6 alkxoycarobnyl; R3, R4, and R5 are each H or C1 -C5 alkyl; R6 is H, halogen, or C1 -C5 alkyl; R7, R8, R9, and R10 are each H or C1 -C5 alkyl; R11 is H, C1 -C5 alkyl, C1 -C5 alkoxy, C2 -C6 alkenyl, C6 -C10 aryl, C7 -C15 aryloxyalkyl, or C7 -C15 aralkyl; R12 and R13 are each H or C1 -C5 alkyl; R14 is C1 -C5 alkyl, C2 -C6 alkenyl, C5 -C10 aryl, or C7 -C15 aralkyl; or R13 and R14 taken together form C3 -C4 alkylene, V1 and V2 are each H, halogen, NO2, CN, or CF3 ; V3 is halogen or CF3 ; W1 is --O-- or --NH--; W2 is --(CH2)n -- wherein n is 0 or 1, or CO; X1 is halogen, or a salt thereof, which is effective as a herbicidal agent.