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o-Toluenesulfonamide, 5-fluoro(6CI,8CI) is a chemical compound characterized by the molecular formula C7H8FNO2S. It is a derivative of sulfonamide that incorporates a fluorine atom, which contributes to its unique reactivity and pharmaceutical properties. o-Toluenesulfonamide, 5-fluoro(6CI,8CI) is recognized for its role as a building block in the synthesis of biologically active molecules, particularly within the pharmaceutical and agrochemical sectors.

2339-57-3

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2339-57-3 Usage

Uses

Used in Pharmaceutical Industry:
o-Toluenesulfonamide, 5-fluoro(6CI,8CI) is utilized as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and reactivity make it a valuable component in the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical sector, o-Toluenesulfonamide, 5-fluoro(6CI,8CI) is employed as a precursor for the production of agrochemicals. Its potential antifungal and antibacterial properties are leveraged to create compounds that can protect crops from diseases and pests, thereby enhancing agricultural productivity.
Used in Medicinal Chemistry Research:
o-Toluenesulfonamide, 5-fluoro(6CI,8CI) serves as a versatile building block in medicinal chemistry research. Its incorporation into various molecular frameworks allows for the exploration of new chemical space and the discovery of novel biologically active compounds with potential therapeutic applications.
Used in Drug Development:
o-Toluenesulfonamide, 5-fluoro(6CI,8CI) is used in drug development as a starting material for the synthesis of new pharmaceutical agents. Its unique properties and reactivity enable the creation of diverse drug candidates that can address unmet medical needs and offer innovative treatment options for various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 2339-57-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,3 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2339-57:
(6*2)+(5*3)+(4*3)+(3*9)+(2*5)+(1*7)=83
83 % 10 = 3
So 2339-57-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H8FNO2S/c1-5-2-3-6(8)4-7(5)12(9,10)11/h2-4H,1H3,(H2,9,10,11)

2339-57-3SDS

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 5-fluoro-2-methylbenzenesulfonamide

1.2 Other means of identification

Product number -
Other names 4-Fluor-toluol-2-sulfonsaeure-amid

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:2339-57-3 SDS

2339-57-3Relevant articles and documents

Discovery of cyclic sulfonamide derivatives as potent inhibitors of SARS-CoV-2

Shin, Young Sup,Lee, Jun Young,Noh, Soojin,Kwak, Yoonna,Jeon, Sangeun,Kwon, Sunoh,Jin, Young-hee,Jang, Min Seong,Kim, Seungtaek,Song, Jong Hwan,Kim, Hyoung Rae,Park, Chul Min

supporting information, (2020/11/13)

Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) continues to spread worldwide, with 25 million confirmed cases and 800 thousand deaths. Effective treatments to target SARS-CoV-2 are urgently needed. In the present study, we have identified a

DERIVATIVES OF BENZOTHIAZINES, PREPARATION THEREOF AND APPLICATION THEREOF AS DRUGS

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Page/Page column 38-39, (2010/09/18)

The object of the present invention is benzothiazine derivatives having the capability of inhibiting 11β-HSD1 not only at an enzymatic level but also at a cell level. The compounds of the present invention are of general formula (I). Wherein notably R1 represents a hydrogen or OR1 represents an ester or an ether. R2 represents a naphthyl or a 1, 2, 3, 4-tetrahydro-naphthalene or a biphenyl or phenyl pyridine or a substituted phenyl. R3 represents a methyl or ethyl; R4 and R'4 represent a hydrogen.

Substituted N-{3-[(1,1-dioxido-1,2-benzothiazol-3-yl)(phenyl)amino]propyl} benzamide analogs as potent Kv1.3 ion channel blockers. Part 2

Haffner, Curt D.,Thomson, Stephen A.,Guo, Yu,Petrov, Kimberly,Larkin, Andrew,Banker, Pierette,Schaaf, Gregory,Dickerson, Scott,Gobel, Jeff,Gillie, Dan,Condreay, J. Patrick,Poole, Chuck,Carpenter, Tiffany,Ulrich, John

scheme or table, p. 6989 - 6992 (2011/02/23)

We report the synthesis and in vitro activity of a series of novel substituted N-{3-[(1,1-dioxido-1,2-benzothiazol-3-yl)(phenyl)amino]propyl} benzamide analogs. These analogs showed potent inhibitory activity against Kv1.3. Several demonstrated similar po

HIV INTEGRASE INHIBITORS

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Page/Page column 12, (2010/11/27)

The invention encompasses a series bicyclic pyrimidinone compounds of Formula I which inhibit HIV integrase and prevent viral integration into human DNA. This action makes the compounds useful for treating HIV infection and AIDS. The invention also encompasses pharmaceutical compositions and methods for treating those infected with HIV.

HIV integrase inhibitors

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Page/Page column 16, (2010/11/27)

The invention encompasses a series bicyclic pyrimidinone compounds of Formula I which inhibit HIV integrase and prevent viral integration into human DNA. This action makes the compounds useful for treating HIV infection and AIDS. The invention also encompasses pharmaceutical compositions and methods for treating those infected with HIV.

BICYCLIC HETEROCYCLES AS HIV INTEGRASE INHIBITORS

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Page/Page column 115, (2010/11/27)

The invention encompasses a series cyclic bicyclic pyrimidinone compounds of Formula I which inhibit HIV integrase and prevent viral integration into human DNA. This action makes the compounds useful for treating HIV infection and AIDS. The invention also encompasses pharmaceutical compositions and methods for treating those infected with HIV.

Bicyclic heterocycles as HIV integrase inhibitors

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Page/Page column 54, (2008/06/13)

The invention encompasses a series cyclic bicyclic pyrimidinone compounds of Formula I which inhibit HIV integrase and prevent viral integration into human DNA. This action makes the compounds useful for treating HIV infection and AIDS. The invention also encompasses pharmaceutical compositions and methods for treating those infected with HIV.

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