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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)-

7-Isoquinolinecarboxaldehyde, 1-chloro-

O=Cc1ccc2c(c1)c(Cl)ncc2 Request for Quotation
Chemical Name: 7-Isoquinolinecarboxaldehyde, 1-chloro-
CAS Number: 223671-53-2
Product Number: AG003E8C(AGN-PC-037D6X)
Synonyms:
MDL No:
Molecular Formula: C10H6ClNO
Molecular Weight: 191.6137

Identification/Properties

Properties
BP:
368.4°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
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
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-Chloroisoquinoline-7-carbaldehyde, also known as $name$, is a versatile compound widely employed in chemical synthesis for its unique reactivity and functional group compatibility. With its chloro group situated at the 1-position and an aldehyde moiety at the 7-position on the isoquinoline ring, this compound serves as a valuable building block in the synthesis of various complex organic molecules.One of the key applications of 1-Chloroisoquinoline-7-carbaldehyde is in the preparation of heterocyclic compounds. By utilizing the reactivity of the chlorine atom and the electrophilicity of the aldehyde group, this compound can participate in a range of reactions such as nucleophilic substitutions, condensations, and cyclizations to introduce diverse functional groups and structural motifs into the final products. This versatility makes it particularly useful in the synthesis of pharmaceuticals, agrochemicals, and materials with tailored properties.Furthermore, 1-Chloroisoquinoline-7-carbaldehyde can act as a valuable intermediate in the construction of biologically active molecules and natural products. Its strategic placement of functional groups allows for precise modification and manipulation of the isoquinoline scaffold to access target compounds with improved potency, selectivity, and pharmacokinetic properties. Overall, the application of this compound in chemical synthesis offers chemists a powerful tool for designing and crafting new molecules with desired characteristics and functionalities.