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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)-

4-chloro-1H-pyrrolo[2,3-b]pyridin-5-ol

Oc1cnc2c(c1Cl)cc[nH]2 Request for Quotation
Chemical Name: 4-chloro-1H-pyrrolo[2,3-b]pyridin-5-ol
CAS Number: 1020056-82-9
Product Number: AG0006AJ(AGN-PC-0NLWCC)
Synonyms:
MDL No:
Molecular Formula: C7H5ClN2O
Molecular Weight: 168.5804

Identification/Properties

Computed Properties
Molecular Weight:
168.58g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
168.009g/mol
Monoisotopic Mass:
168.009g/mol
Topological Polar Surface Area:
48.9A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
155
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#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Chloro-1H-pyrrolo[2,3-b]pyridin-5-ol is a versatile compound commonly used in chemical synthesis due to its unique structure and properties. In organic chemistry, this compound serves as a valuable building block for the synthesis of various heterocyclic compounds and pharmaceutical intermediates. Its reactive chlorine moiety allows for easy functionalization and derivatization, making it a valuable starting material for the preparation of diverse chemical compounds. Additionally, 4-Chloro-1H-pyrrolo[2,3-b]pyridin-5-ol can participate in a variety of key chemical reactions such as nucleophilic substitution, cyclization, and cross-coupling reactions, enabling the formation of complex molecular structures. Its utility in medicinal chemistry and agrochemical research further showcases its significance in the field of chemical synthesis.