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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-Pyrrolo[2,3-b]pyridine, 4-chloro-2-methyl-

Cc1cc2c([nH]1)nccc2Cl Request for Quotation
Chemical Name: 1H-Pyrrolo[2,3-b]pyridine, 4-chloro-2-methyl-
CAS Number: 307951-53-7
Product Number: AG0031AD(AGN-PC-035JHL)
Synonyms:
MDL No:
Molecular Formula: C8H7ClN2
Molecular Weight: 166.6076

Identification/Properties

Computed Properties
Molecular Weight:
166.608g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
166.03g/mol
Monoisotopic Mass:
166.03g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
151
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Chloro-2-methyl-1H-pyrrolo[2,3-b]pyridine serves as a valuable building block in chemical synthesis due to its distinct molecular structure and reactivity. This compound is commonly employed as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and various organic molecules. Its unique pyrrolopyridine scaffold allows for diverse functionalizations, making it a versatile tool in the preparation of complex organic compounds. In addition, the presence of the chlorine and methyl substituents in its structure offers opportunities for further manipulation and derivatization, enabling the synthesis of novel compounds with specific properties and functionalities. Overall, the strategic incorporation of 4-Chloro-2-methyl-1H-pyrrolo[2,3-b]pyridine in chemical synthesis enables the efficient and strategic construction of diverse molecular architectures for various applications in the field of chemistry.