1. Home
  2. 1H-Pyrrolo[2,3-c]pyridine-2-carboxylic acid, ethyl ester

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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-c]pyridine-2-carboxylic acid, ethyl ester

CCOC(=O)c1cc2c([nH]1)cncc2 Request for Quotation
Chemical Name: 1H-Pyrrolo[2,3-c]pyridine-2-carboxylic acid, ethyl ester
CAS Number: 24334-19-8
Product Number: AG0037HT(AGN-PC-03G3RY)
Synonyms:
MDL No:
Molecular Formula: C10H10N2O2
Molecular Weight: 190.1986

Identification/Properties

Properties
BP:
371.8°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
190.202g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
190.074g/mol
Monoisotopic Mass:
190.074g/mol
Topological Polar Surface Area:
55A^2
Heavy Atom Count:
14
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

Request for Quotation

Customer Feedback

Chemical Structure


Ethyl 1H-pyrrolo[2,3-c]pyridine-2-carboxylate is a versatile compound widely utilized in chemical synthesis for its unique properties. This particular molecule serves as a crucial building block in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Due to its structural features and reactivity, it acts as a key intermediate in the formation of complex organic compounds through different synthetic methodologies such as esterification, amidation, and cyclization reactions. Its presence enables the rapid and efficient construction of diverse molecular architectures, making it an indispensable tool for organic chemists in the preparation of novel compounds with potential biological activities or industrial applications.