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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)-

1H-Indole-2-carboxylic acid, 6-chloro-, methyl ester

COC(=O)c1cc2c([nH]1)cc(cc2)Cl Request for Quotation
Chemical Name: 1H-Indole-2-carboxylic acid, 6-chloro-, methyl ester
CAS Number: 98081-84-6
Product Number: AG0069X7(AGN-PC-0LFZ6X)
Synonyms:
MDL No:
Molecular Formula: C10H8ClNO2
Molecular Weight: 209.6290

Identification/Properties

Properties
BP:
365.5°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
209.629g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
209.024g/mol
Monoisotopic Mass:
209.024g/mol
Topological Polar Surface Area:
42.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
234
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-H317
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 6-chloro-1H-indole-2-carboxylate is a versatile compound commonly utilized in chemical synthesis for the creation of novel pharmaceuticals, agrochemicals, and fine chemicals. This compound serves as a crucial building block in the development of various organic compounds due to its unique structure and reactivity. Known for its ability to participate in diverse chemical reactions, Methyl 6-chloro-1H-indole-2-carboxylate is particularly valued in the synthesis of indole derivatives, which are widely applied in medicinal chemistry and material science. Through strategic manipulation of its functional groups, this compound can be transformed into a wide range of derivatives with tailored properties, making it an indispensable tool for synthetic chemists seeking to design and fabricate innovative molecules with specific functions and applications.