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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)-

Methyl6-chloro-1H-pyrrolo[3,2-b]pyridine-3-carboxylate

COC(=O)c1c[nH]c2c1ncc(c2)Cl Request for Quotation
Chemical Name: Methyl6-chloro-1H-pyrrolo[3,2-b]pyridine-3-carboxylate
CAS Number: 959245-12-6
Product Number: AG006A53(AGN-PC-0WALLY)
Synonyms:
MDL No:
Molecular Formula: C9H7ClN2O2
Molecular Weight: 210.6171

Identification/Properties

Properties
BP:
362.9°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
210.617g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
210.02g/mol
Monoisotopic Mass:
210.02g/mol
Topological Polar Surface Area:
55A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
237
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-H317-H319-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 6-chloro-1H-pyrrolo[3,2-b]pyridine-3-carboxylate is a versatile compound commonly used in chemical synthesis as a key intermediate for the production of pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and reactivity make it a valuable building block in the preparation of various heterocyclic compounds with potential biological activities. This compound serves as a crucial starting material for the synthesis of pyrrolopyridines, which are important structural motifs found in many biologically active compounds. By incorporating Methyl 6-chloro-1H-pyrrolo[3,2-b]pyridine-3-carboxylate into synthetic pathways, chemists can access a wide range of complex molecules with diverse functionalities, making it an indispensable tool in organic synthesis.