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3,3'-Sulfonylbis[6-fluoroaniline] is a chemical compound belonging to the class of anilines, which are derivatives of benzene. It is characterized by the presence of two fluorine atoms and a sulfone group attached to a central benzene ring, with the chemical formula C12H10F2N2O2S.

40939-65-9

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40939-65-9 Usage

Uses

Used in Pharmaceutical Industry:
3,3'-Sulfonylbis[6-fluoroaniline] is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of various medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical industry, 3,3'-Sulfonylbis[6-fluoroaniline] serves as an intermediate, playing a role in the creation of substances that aid in the management and protection of crops.
Used in Dye Industry:
3,3'-Sulfonylbis[6-fluoroaniline] is utilized as an intermediate in the production of dyes, contributing to the coloration and properties of various dye products.
Safety Note:
Due to its toxicological properties, 3,3'-Sulfonylbis[6-fluoroaniline] may pose health risks if not handled properly. It is crucial to follow proper safety measures when working with 3,3'-Sulfonylbis[6-fluoroaniline] to avoid any potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 40939-65-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,9,3 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40939-65:
(7*4)+(6*0)+(5*9)+(4*3)+(3*9)+(2*6)+(1*5)=129
129 % 10 = 9
So 40939-65-9 is a valid CAS Registry Number.

40939-65-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(3-amino-4-fluorophenyl)sulfonyl-2-fluoroaniline

1.2 Other means of identification

Product number -
Other names Benzenamine,3,3'-sulfonylbis[6-fluoro

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:40939-65-9 SDS

40939-65-9Relevant academic research and scientific papers

SUSTAINABLE CHEMICAL PROCESS FOR REDUCTION OF NITRO COMPOUNDS (R-NO2) OR NITROSO COMPOUNDS (R-NO) CONTAINING SULPHONIC OR CARBOXYLIC GROUP INTO CORRESPONDING AMINO COMPOUNDS (R-NH2) WITH INHERENT RECYCLE OF ALL ACIDIC STREAMS GENERATED IN SYNTHESIS

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Page/Page column 51; 53-54, (2011/05/06)

The process of the present invention creates a sustainable and closed water loop allowing inherent recycles of all liquid streams generated in the process. The liquid streams generated during the process of the invention are inherently recycled completely, making the process of the present invention a zero liquid discharge process which is environmentally friendly and sustainable. This invention further relates to a sustainable chemical process of reduction of R- NO2 or R-NO into corresponding R-NH2 that produces environmentally friendly R-NH2 in good yields and selectivity with large of mother liquor recycle. The process has a wide scope in that it can be applied to a number of molecules.

Antiparasitic Agents: Part 5 - Synthesis of 4-(Substituted-aryl)amino-7-chloroquinolines as Potential Antimalarial Agents

Chauhan, P. M. S.,Sharma, Satyavan,Bhakuni, D. S.

, p. 1142 - 1145 (2007/10/02)

A series of 4-(4- and 3-substituted-aryl)amino-7-chloroquinolines (11-15, 17, 18, 28) and substituted diphenyl sulphones (8-10, 19-27) have been synthesized and tested for their antiparasitic activity against Plasmodium berghei in mice, Litomosoides carinii in cotton rats and Hymenolepis nana in mice.Of the compounds tested, 11 shows 100percent activity against P. berghei at a dose of 10 mg/kg x 5 days in mice while 23 is effective in eliminating 100percent of the H. nana worms from mice at a single oral dose of 250 mg/kg.

Anti-allergic oxanilate compounds

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, (2008/06/13)

A method of treating mammals for allergy and anaphylactic reactions of a reagin or non-reagin mediated nature which comprises administering prophylactically to said mammal an anti-allergy or anaphylactic reaction effective amount of a compound of the formula STR1 Novel compounds and compositions are also claimed.

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