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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)-

5-methoxy-2-oxo-1,3-dihydroindole-3-carbaldehyde

O=CC1C(=O)Nc2c1cc(OC)cc2 Request for Quotation
Chemical Name: 5-methoxy-2-oxo-1,3-dihydroindole-3-carbaldehyde
CAS Number: 52508-88-0
Product Number: AG00DCZC(AGN-PC-07HBWT)
Synonyms:
MDL No:
Molecular Formula: C10H9NO3
Molecular Weight: 191.1834

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Computed Properties
Molecular Weight:
191.186g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
191.058g/mol
Monoisotopic Mass:
191.058g/mol
Topological Polar Surface Area:
55.4A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
254
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Methoxy-2-oxoindoline-3-carbaldehyde is a versatile compound widely used in chemical synthesis, particularly in the creation of various organic compounds. This compound serves as a key building block in the synthesis of complex molecules due to its unique structural properties and reactivity.One significant application of 5-Methoxy-2-oxoindoline-3-carbaldehyde is its use as a precursor in the synthesis of indole derivatives. Indole derivatives have diverse applications in medicinal chemistry, agrochemicals, and materials science. By utilizing 5-Methoxy-2-oxoindoline-3-carbaldehyde as a starting material, chemists can introduce specific functional groups and stereochemistry to the indole scaffold, thereby enabling the synthesis of novel compounds with tailored properties.Additionally, 5-Methoxy-2-oxoindoline-3-carbaldehyde can participate in various multicomponent reactions and functional group transformations, further expanding its utility in chemical synthesis. Its ability to undergo selective reactions makes it a valuable tool for constructing complex molecular architectures efficiently.Overall, 5-Methoxy-2-oxoindoline-3-carbaldehyde is a crucial intermediate in organic synthesis, enabling chemists to access a wide range of functionalized compounds with diverse applications. Its versatility and reactivity make it a valuable asset in the toolkit of synthetic chemists seeking to diversify and expand their molecular design capabilities.