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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)-

4-Isoquinolinecarboxaldehyde, 3-chloro-

O=Cc1c(Cl)ncc2c1cccc2 Request for Quotation
Chemical Name: 4-Isoquinolinecarboxaldehyde, 3-chloro-
CAS Number: 120285-29-2
Product Number: AG0094KX(AGN-PC-001TV5)
Synonyms:
MDL No:
Molecular Formula: C10H6ClNO
Molecular Weight: 191.6137

Identification/Properties

Computed Properties
Molecular Weight:
191.614g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
191.014g/mol
Monoisotopic Mass:
191.014g/mol
Topological Polar Surface Area:
30A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
197
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


$Name$ is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. As a key building block in organic chemistry, 3-Chloroisoquinoline-4-carbaldehyde plays a crucial role in the development of various pharmaceuticals, agrochemicals, and materials. Its presence in the synthesis of complex molecules allows for precise control over the chemical reactions, leading to the formation of new compounds with specific functionalities.One of the primary applications of 3-Chloroisoquinoline-4-carbaldehyde is in the construction of heterocyclic structures. By incorporating this compound into reaction schemes, chemists can introduce the chloro group at specific positions within the molecular framework, enabling the creation of diverse chemical entities with enhanced biological activities. Additionally, the presence of the aldehyde functional group in 3-Chloroisoquinoline-4-carbaldehyde offers opportunities for further derivatization, facilitating the synthesis of more complex molecules.Furthermore, 3-Chloroisoquinoline-4-carbaldehyde serves as a valuable intermediate in the preparation of various biologically active compounds such as pharmaceutical intermediates and natural product derivatives. Its compatibility with a wide range of chemical reactions allows for the efficient assembly of intricate molecular structures, making it a crucial component in modern organic synthesis. Overall, the strategic incorporation of 3-Chloroisoquinoline-4-carbaldehyde in chemical synthesis enables chemists to access a diverse array of functionalized molecules with potential applications in drug discovery, materials science, and other fields.