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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)-

ethyl 1H-pyrrolo[2,3-c]pyridine-3-carboxylate

CCOC(=O)c1c[nH]c2c1ccnc2 Request for Quotation
Chemical Name: ethyl 1H-pyrrolo[2,3-c]pyridine-3-carboxylate
CAS Number: 67058-73-5
Product Number: AG0064DR(AGN-PC-0LOT0I)
Synonyms:
MDL No:
Molecular Formula: C10H10N2O2
Molecular Weight: 190.1986

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;

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


Ethyl 1H-pyrrolo[2,3-c]pyridine-3-carboxylate is a valuable compound that finds versatile applications in chemical synthesis processes. This intermediate is commonly used in the synthesis of various heterocyclic compounds due to its functional group reactivity and structural versatility. In organic synthesis, Ethyl 1H-pyrrolo[2,3-c]pyridine-3-carboxylate serves as a key building block for the construction of complex molecules and pharmaceutical compounds. Its unique molecular structure allows for diverse functionalization and modification, making it a valuable tool in the creation of novel chemical entities. Researchers and chemists often utilize this compound to introduce specific chemical functionalities or structural motifs into target molecules, enabling them to access new chemical space and develop innovative synthetic pathways. Its application in chemical synthesis extends to the development of new materials, agrochemicals, and pharmaceuticals, highlighting its significance in advancing various scientific fields.