10372-41-5 Usage
Description
3-AMINO-N,N-DIETHYL-BENZENESULFONAMIDE, also known as 3-Amino-N,N-diethylbenzenesulfonamide, is an organic compound with the molecular formula C8H12N2O2S. It is a derivative of benzenesulfonamide, featuring an amino group and two diethyl groups attached to the nitrogen atoms. 3-AMINO-N,N-DIETHYL-BENZENESULFONAMIDE is known for its anticonvulsant properties and is commonly utilized as a pharmaceutical and research intermediate.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 10372-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,7 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10372-41:
(7*1)+(6*0)+(5*3)+(4*7)+(3*2)+(2*4)+(1*1)=65
65 % 10 = 5
So 10372-41-5 is a valid CAS Registry Number.
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
10372-41-5Relevant articles and documents
A simple synthesis of anilines by LiAlH4/TiCl4 reduction of aromatic nitro compounds
Di Gioia, Maria Luisa,Leggio, Antonella,Guarino, Isabella Federica,Leotta, Vanessa,Romio, Emanuela,Liguori, Angelo
, p. 5341 - 5344 (2015)
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.
