1. Home
  2. 1H-Indole-4-carboxylic acid, 6-amino-, methyl ester, monohydrochloride

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-Indole-4-carboxylic acid, 6-amino-, methyl ester, monohydrochloride

COC(=O)c1cc(N)cc2c1cc[nH]2.Cl Request for Quotation
Chemical Name: 1H-Indole-4-carboxylic acid, 6-amino-, methyl ester, monohydrochloride
CAS Number: 731810-08-5
Product Number: AG00FFVZ(AGN-PC-0U2ELD)
Synonyms:
MDL No:
Molecular Formula: C10H11ClN2O2
Molecular Weight: 226.6595

Identification/Properties

Computed Properties
Molecular Weight:
226.66g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
226.051g/mol
Monoisotopic Mass:
226.051g/mol
Topological Polar Surface Area:
68.1A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
232
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Methyl 6-amino-1H-indole-4-carboxylate hydrochloride is a versatile compound widely utilized in chemical synthesis for its significant role as a key building block in the production of various pharmaceuticals and fine chemicals. This compound serves as a crucial intermediate in the synthesis of biologically active molecules, particularly those with indole-based structures. Its presence in synthetic pathways allows for the strategic introduction of the amino and carboxylate functional groups, enabling the modification and diversification of molecular structures to generate novel compounds with desired properties. By incorporating Methyl 6-amino-1H-indole-4-carboxylate hydrochloride into chemical reactions, researchers can access a wide range of derivatives with potential applications in drug discovery, medicinal chemistry, and material science.