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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-3-acetic acid, monosodium salt

[O-]C(=O)Cc1c[nH]c2c1cccc2.[Na+] Request for Quotation
Chemical Name: 1H-Indole-3-acetic acid, monosodium salt
CAS Number: 6505-45-9
Product Number: AG00IBFT(AGN-PC-0TF5HW)
Synonyms:
MDL No:
Molecular Formula: C10H8NNaO2
Molecular Weight: 197.1658

Identification/Properties

Computed Properties
Molecular Weight:
197.17g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
197.045273g/mol
Monoisotopic Mass:
197.045273g/mol
Topological Polar Surface Area:
55.9Ų
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
210
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Sodium 2-(1H-indol-3-yl)acetate, a versatile chemical compound commonly used in chemical synthesis, plays a critical role in various organic reactions due to its unique structural properties. This compound serves as an essential building block in the synthesis of pharmaceuticals, agrochemicals, and other complex organic molecules. One of the key applications of Sodium 2-(1H-indol-3-yl)acetate lies in its utility as a precursor for indole-containing compounds, which are widely used in the pharmaceutical industry for the synthesis of drugs targeting various diseases. Its ability to undergo diverse transformations, such as functional group manipulations and carbon-carbon bond formations, makes it a valuable tool in the production of bioactive molecules with potential therapeutic properties. Furthermore, Sodium 2-(1H-indol-3-yl)acetate can be employed in the synthesis of natural products, dyes, and functional materials, highlighting its versatility as a building block in synthetic organic chemistry. Its ease of manipulation and compatibility with a variety of reaction conditions make it a valuable reagent for chemists seeking to access a wide range of chemical structures efficiently. In summary, Sodium 2-(1H-indol-3-yl)acetate is a crucial component in chemical synthesis, enabling the construction of diverse organic molecules with applications in pharmaceuticals, materials science, and other industries. Its role as a key intermediate underscores its importance in modern synthetic chemistry research.