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10372-41-5

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10372-41-5 Usage

Uses

3-Amino-N,N-dimethylbenzenesulfonamide exhibits anticonvulsant activity in epileptic conditions. A useful pharmaceutical and research intermediate.

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

10372-41-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Amino-N,N-diethylbenzenesulfonamide

1.2 Other means of identification

Product number -
Other names N,N-Diethyl 3-aminobenzenesulfonamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10372-41-5 SDS

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.

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