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AA92161

173903-47-4 | Benzamide, 2-hydroxy-N-(5-nitro-2-thiazolyl)-

Packsize Purity Availability Price Discounted Price    Quantity
1mg 90% in stock $33.00 $23.00 -   +
250mg 90% in stock $59.00 $41.00 -   +
1g 90% in stock $120.00 $84.00 -   +
5g 90% in stock $335.00 $234.00 -   +
25g 90% in stock $1,205.00 $843.00 -   +

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Description
Catalog Number: AA92161
Chemical Name: Benzamide, 2-hydroxy-N-(5-nitro-2-thiazolyl)-
CAS Number: 173903-47-4
Molecular Formula: C10H7N3O4S
Molecular Weight: 265.2453
MDL Number: MFCD07484970
SMILES: O=C(c1ccccc1O)Nc1ncc(s1)[N+](=O)[O-]
NSC Number: 697856

 

Computed Properties
Complexity: 336  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 18  
Hydrogen Bond Acceptor Count: 6  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 2  
XLogP3: 3.2  

 

 

Upstream Synthesis Route 
  • 2-Hydroxy-N-(5-nitro-2-thiazolyl)benzamide is a versatile compound widely used in chemical synthesis as a key building block for various organic reactions. This compound is known for its ability to participate in a range of synthetic processes, primarily due to the presence of functional groups that allow for diverse chemical transformations.In chemical synthesis, 2-Hydroxy-N-(5-nitro-2-thiazolyl)benzamide serves as a crucial intermediate in the creation of pharmaceuticals, agrochemicals, and specialty chemicals. Its structural features and reactivity make it an essential reagent for the formation of new carbon-carbon and carbon-heteroatom bonds in organic molecules.Furthermore, the presence of the hydroxyl group in 2-Hydroxy-N-(5-nitro-2-thiazolyl)benzamide enables it to act as a nucleophile or a hydrogen bond donor in various reactions. This characteristic enhances its utility in synthetic transformations such as esterifications, amidations, and nucleophilic substitutions.Moreover, the nitro and thiazolyl moieties in the compound provide opportunities for further functionalization through reduction, oxidation, and coupling reactions. This versatility makes 2-Hydroxy-N-(5-nitro-2-thiazolyl)benzamide a valuable tool for customizing molecular structures and achieving specific chemical goals in the laboratory.Overall, the strategic placement of functional groups in 2-Hydroxy-N-(5-nitro-2-thiazolyl)benzamide makes it an indispensable component in the toolbox of synthetic chemists, enabling the efficient construction of complex molecules and the exploration of new chemical pathways.
Literature
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