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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, 4-chloro-

Clc1cccc2c1cn[nH]2 Request for Quotation
Chemical Name: 1H-Indazole, 4-chloro-
CAS Number: 13096-96-3
Product Number: AG000V6B(AGN-PC-0JQ4GK)
Synonyms:
MDL No:
Molecular Formula: C7H5ClN2
Molecular Weight: 152.5810

Identification/Properties

Computed Properties
Molecular Weight:
152.581g/mol
XLogP3:
2.2
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Chloro-1H-indazole is a versatile building block in chemical synthesis, commonly utilized in the pharmaceutical and agrochemical industries. Its unique structure and reactivity make it a valuable tool for constructing complex organic molecules. In organic synthesis, 4-Chloro-1H-indazole serves as a key intermediate for the preparation of various biologically active compounds, including potential drugs and crop protection agents. With its functional group compatibility and propensity for selective reactions, this compound enables efficient and precise modification of molecular structures, facilitating the development of novel chemicals with desired properties. Whether used in medicinal chemistry research or agrochemical development, 4-Chloro-1H-indazole offers synthetic chemists a strategic pathway to create diverse and valuable products.