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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1H-Indazole, 5-chloro-

Clc1ccc2c(c1)cn[nH]2 Request for Quotation
Chemical Name: 1H-Indazole, 5-chloro-
CAS Number: 698-26-0
Product Number: AG003MLQ(AGN-PC-0JL96T)
Synonyms:
MDL No:
Molecular Formula: C7H5ClN2
Molecular Weight: 152.5810

Identification/Properties

Properties
MP:
144 - 146 °C
BP:
309.5 °C at 760 mmHg.
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
152.581g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
152.014g/mol
Monoisotopic Mass:
152.014g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
129
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


1H-Indazole, 5-chloro- is a key building block in chemical synthesis due to its versatile reactivity and structural features. This compound is widely utilized in the pharmaceutical industry as a valuable intermediate for the synthesis of various biologically active compounds. In particular, its unique functional groups and aromatic ring system make it an essential component in the development of pharmaceuticals, agrochemicals, and materials science.In organic synthesis, 1H-Indazole, 5-chloro- serves as a valuable starting material for the construction of complex molecular structures through various chemical transformations. Its chloro-substituted position provides a handle for further functionalization, allowing for the introduction of diverse chemical groups to fine-tune the properties of the final product. This compound can participate in substitution, addition, and coupling reactions to form new carbon-carbon and carbon-heteroatom bonds, enabling the creation of novel molecules with desired properties.Moreover, 1H-Indazole, 5-chloro- exhibits interesting biological activities and has been studied for its potential pharmacological effects. By incorporating this compound into drug design, researchers can explore its interactions with biological targets and evaluate its potential therapeutic applications. Its structural similarity to naturally occurring bioactive molecules makes it a promising candidate for drug discovery and development.Overall, the application of 1H-Indazole, 5-chloro- in chemical synthesis offers a wide range of opportunities for creating diverse molecules with pharmaceutical, agrochemical, and material applications. Its versatility and reactivity make it a valuable tool for chemists and researchers seeking to explore new avenues in organic chemistry and drug development.