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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)-

1-oxo-2,3-dihydroisoindole-5-carbaldehyde

O=Cc1ccc2c(c1)CNC2=O Request for Quotation
Chemical Name: 1-oxo-2,3-dihydroisoindole-5-carbaldehyde
CAS Number: 926307-99-5
Product Number: AG0036WW(AGN-PC-0J0Y6I)
Synonyms:
MDL No:
Molecular Formula: C9H7NO2
Molecular Weight: 161.1574

Identification/Properties

Properties
BP:
493.8±45.0°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
161.16g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
161.048g/mol
Monoisotopic Mass:
161.048g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
215
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Oxoisoindoline-5-carbaldehyde is a versatile compound widely used in chemical synthesis due to its unique reactivity and functional group compatibility. In organic chemistry, it serves as a key building block for the formation of various heterocyclic compounds and pharmaceutical intermediates. This compound is particularly valued for its ability to undergo diverse transformations such as condensation reactions, nucleophilic additions, and oxidative processes. Its application extends to the synthesis of biologically active molecules, agrochemicals, and materials science. Additionally, 1-Oxoisoindoline-5-carbaldehyde plays a crucial role in the development of novel synthetic methodologies and the exploration of new chemical reactions. As a valuable tool in the hands of synthetic chemists, this compound enables the efficient assembly of complex molecular structures with high precision and control.