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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)-

6-chloro-3-nitro-1H-pyrrolo[2,3-b]pyridine

Clc1ccc2c(n1)[nH]cc2[N+](=O)[O-] Request for Quotation
Chemical Name: 6-chloro-3-nitro-1H-pyrrolo[2,3-b]pyridine
CAS Number: 1190309-92-2
Product Number: AG000P46(AGN-PC-09RUYN)
Synonyms:
MDL No:
Molecular Formula: C7H4ClN3O2
Molecular Weight: 197.5786

Identification/Properties

Computed Properties
Molecular Weight:
197.578g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
196.999g/mol
Monoisotopic Mass:
196.999g/mol
Topological Polar Surface Area:
74.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
220
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


6-Chloro-3-nitro-1H-pyrrolo[2,3-b]pyridine, also known as $name$, plays a crucial role in chemical synthesis as a valuable building block. This compound is widely utilized in the pharmaceutical and agrochemical industries for the preparation of various biologically active molecules.One of the key applications of 6-Chloro-3-nitro-1H-pyrrolo[2,3-b]pyridine in chemical synthesis is its use as a key intermediate in the synthesis of heterocyclic compounds. It serves as a versatile starting material for the construction of complex molecular structures, allowing chemists to access a diverse range of target compounds with desired properties.Furthermore, 6-Chloro-3-nitro-1H-pyrrolo[2,3-b]pyridine is often employed in the development of novel pharmaceutical agents and crop protection chemicals. Its unique structural features enable the modification of its chemical structure through various synthetic transformations, leading to the creation of new molecules with enhanced biological activities.Overall, the versatility and synthetic utility of 6-Chloro-3-nitro-1H-pyrrolo[2,3-b]pyridine make it a valuable tool in the hands of chemists engaged in the synthesis of biologically relevant compounds and functional materials.