1. Home
  2. 1H-Indole-2-carboxylic acid, 4-methyl-, ethyl ester

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-Indole-2-carboxylic acid, 4-methyl-, ethyl ester

CCOC(=O)c1cc2c([nH]1)cccc2C Request for Quotation
Chemical Name: 1H-Indole-2-carboxylic acid, 4-methyl-, ethyl ester
CAS Number: 16732-80-2
Product Number: AG001XBQ(AGN-PC-0NJAP8)
Synonyms:
MDL No:
Molecular Formula: C12H13NO2
Molecular Weight: 203.2371

Identification/Properties

Computed Properties
Molecular Weight:
203.241g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
203.095g/mol
Monoisotopic Mass:
203.095g/mol
Topological Polar Surface Area:
42.1A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
242
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

Request for Quotation

Customer Feedback

Chemical Structure


Ethyl 4-methyl-1H-indole-2-carboxylate is a versatile compound widely used in chemical synthesis. It serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals due to its unique structural features and reactivity. This compound is particularly valued for its role as a precursor in the synthesis of indole-based compounds, which are important in the development of biologically active molecules such as anticancer agents, antibiotics, and anti-inflammatory drugs. Its incorporation into chemical reactions allows for the introduction of the indole moiety, enabling the formation of complex molecular structures with diverse functionalities. In addition, the ester group in Ethyl 4-methyl-1H-indole-2-carboxylate provides opportunities for further derivatization, allowing for the modification of properties and enhancement of the compound's biological activity.