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2-Benzylamino-5-trifluoromethyl-benzenesulfonamide is a chemical compound with the molecular formula C14H12F3N2O2S. It is a derivative of benzenesulfonamide, featuring a benzylamine group at the 2-position and a trifluoromethyl group at the 5-position. 2-BENZYLAMINO-5-TRIFLUOROMETHYL-BENZENESULFONAMIDE is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, particularly as an intermediate in the production of various active ingredients. Its structure provides a foundation for further chemical modifications, which can lead to the development of new compounds with specific therapeutic or pesticidal properties.

1698-38-0

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1698-38-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1698-38-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,9 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1698-38:
(6*1)+(5*6)+(4*9)+(3*8)+(2*3)+(1*8)=110
110 % 10 = 0
So 1698-38-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H13F3N2O2S/c15-14(16,17)11-6-7-12(13(8-11)22(18,20)21)19-9-10-4-2-1-3-5-10/h1-8,19H,9H2,(H2,18,20,21)

1698-38-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Benzylamino)-5-(trifluoromethyl)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names 2-benzylamino-5-trifluoromethylbenzenesulfonamide

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:1698-38-0 SDS

1698-38-0Relevant academic research and scientific papers

Effect on KATP channel activation properties and tissue selectivity of the nature of the substituent in the 7- and the 3-position of 4H-1,2,4-benzothiadiazine 1,1-dioxides

Boverie, Stéphane,Antoine, Marie-Hélène,Somers, Fabian,Becker, Bénédicte,Sebille, Sophie,Ouedraogo, Raogo,Counerotte, Stéphane,Pirotte, Bernard,Lebrun, Philippe,De Tullio, Pascal

, p. 3492 - 3503 (2007/10/03)

The present work explored 3-alkylamino-4H-1,2,4-benzothiadiazine 1,1-dioxides diversely substituted in the 7-position. Those compounds, structurally related to previously described potassium channel openers such as the benzothiadiazine dioxide BPDZ 73, we

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