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1801267-04-8

6-Chloro-2-methyl-5-nitro-2H-indazole

Catalog#: AR01XGR7  |   CAS#: 1801267-04-8  |   MDL#: MFCD00237464  |   MF: C8H6ClN3O2  |   MW: 211.6051

Packsize Purity Price Availability Quantity
100mg 97% $14.00 Global Stock Buy Now Add To Cart
250mg 97% $25.00 Global Stock Buy Now Add To Cart
1g 97% $98.00 Global Stock Buy Now Add To Cart
5g 97% $477.00 Global Stock Buy Now Add To Cart
10g 97% $869.00 Global Stock Buy Now Add To Cart
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Catalog Number AR01XGR7
Chemical Name 6-Chloro-2-methyl-5-nitro-2H-indazole
CAS Number 1801267-04-8
Molecular Formula C8H6ClN3O2
Molecular Weight 211.6051
MDL Number MFCD00237464
SMILES Cn1nc2c(c1)cc(c(c2)Cl)N(=O)=O

6-Chloro-2-methyl-5-nitro-2H-indazole is a versatile compound with significant applications in chemical synthesis. This compound serves as a key building block in the construction of various organic molecules, particularly in the pharmaceutical and agrochemical industries. Its unique structure and reactivity make it a valuable intermediate in the synthesis of a wide range of biologically active compounds.One important application of 6-Chloro-2-methyl-5-nitro-2H-indazole is in the synthesis of heterocyclic compounds, which are commonly found in many pharmaceutical drugs. By incorporating this compound into the synthetic route, chemists can introduce specific functional groups and stereochemical features that are crucial for the desired pharmacological activity of the final product. Additionally, the presence of the chloro, methyl, and nitro groups in the molecule enables further derivatization to generate novel compounds with enhanced biological properties.Furthermore, 6-Chloro-2-methyl-5-nitro-2H-indazole can be utilized as a reactive intermediate for the preparation of various nitrogen-containing compounds. Its electron-deficient nature and regioselectivity in reactions make it a valuable tool for the synthesis of complex molecules with multiple nitrogen atoms, such as alkaloids and amino acid derivatives. Chemists can leverage the versatility of this compound to access diverse chemical space and discover new bioactive compounds with potential therapeutic applications.In conclusion, the strategic incorporation of 6-Chloro-2-methyl-5-nitro-2H-indazole in chemical synthesis offers a pathway to access structurally diverse and biologically relevant compounds. Its role as a versatile building block underscores its importance in drug discovery efforts and organic synthesis endeavors.
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