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5-(4-bromo-2-fluorophenyl)-1,3,4-thiadiazol-2-amine is a chemical compound that belongs to the class of organic compounds known as phenyl thiadiazoles. These are aromatic compounds containing a thiadiazole ring substituted by a phenyl group. This particular compound is notable for its bromo and fluoro atom substitutions on the phenyl group, classifying it as a halogenated compound. The thiadiazole ring is a five-membered aromatic ring composed of two nitrogen atoms, two carbon atoms, and one sulfur atom. 5-(4-bromo-2-fluorophenyl)-1,3,4-thiadiazol-2-amine's applications or uses are not commonly noted in literature, which may suggest that it is predominantly used in research or specific chemical reactions. The complexity and specific substitutions of 5-(4-bromo-2-fluorophenyl)-1,3,4-thiadiazol-2-amine likely determine its chemical behavior and reactivity.

299937-74-9

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299937-74-9 Usage

Uses

Used in Research Applications:
5-(4-bromo-2-fluorophenyl)-1,3,4-thiadiazol-2-amine is used as a research chemical for the investigation of its chemical properties and potential applications in various fields. Its unique structure with a thiadiazole ring and halogenated phenyl group may offer specific reactivity or interactions that are of interest to researchers in organic chemistry and related disciplines.
Used in Chemical Reactions:
In the field of organic synthesis, 5-(4-bromo-2-fluorophenyl)-1,3,4-thiadiazol-2-amine may be used as a reactant or intermediate in the preparation of more complex molecules. Its bromo and fluoro substitutions could be key functional groups that participate in reactions such as cross-coupling, nucleophilic substitution, or electrophilic aromatic substitution, leading to the formation of novel compounds with potential applications in pharmaceuticals, materials science, or other areas.
Used in Pharmaceutical Development:
Although not commonly noted in literature, the compound's structure suggests that it could be a candidate for pharmaceutical development. The presence of the thiadiazole ring and halogenated phenyl group may confer biological activity, and researchers may explore its potential as a lead compound in the development of new drugs. 5-(4-bromo-2-fluorophenyl)-1,3,4-thiadiazol-2-amine could be subjected to further modifications and testing to assess its efficacy and safety in various therapeutic applications.
Used in Materials Science:
The unique structural features of 5-(4-bromo-2-fluorophenyl)-1,3,4-thiadiazol-2-amine may also make it a candidate for use in materials science. Its potential applications could include the development of new materials with specific properties, such as electronic, optical, or mechanical characteristics. Researchers may investigate its use in the synthesis of polymers, coatings, or other materials with tailored properties for various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 299937-74-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,9,9,3 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 299937-74:
(8*2)+(7*9)+(6*9)+(5*9)+(4*3)+(3*7)+(2*7)+(1*4)=229
229 % 10 = 9
So 299937-74-9 is a valid CAS Registry Number.

299937-74-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-Bromo-2-fluorophenyl)-1,3,4-thiadiazol-2-amine

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:299937-74-9 SDS

299937-74-9Relevant academic research and scientific papers

FLAP MODULATORS

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Paragraph 0181, (2015/11/03)

The present invention relates to compounds of Formula (I), or a form thereof, wherein ring A, R1, R2, R3, R3′, L, W, and V are as defined herein, useful as FLAP modulators. The invention also relates to pharmaceutical compositions comprising compounds of Formula (I). Methods of making and using the compounds of Formula (I) are also within the scope of the invention

OXAZOLIDINONE DERIVATIVES AS ANTIMICROBIALS

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Page/Page column 68, (2010/10/20)

The present invention relates to certain substituted phenyl oxazolidinones and to processes for the synthesis of the same. This invention also relates to pharmaceutical compositions containing the compounds of the present invention as antimicrobials. The compounds are useful antimicrobial agents, effective against a number of human and veterinary pathogens, including gram-positive aerobic bacteria, for example, multiple-resistant staphylococci, streptococci and enterococci as well as anaerobic organisms, for example, Bacterioides spp. and Clostridia spp. species, and acid fast organisms, for example, Mycobacterium tuberculosis, Mycobacterium avium and Mycobacterium spp.

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