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  2. 1H-Isoindole-1,3(2H)-dione, 2-[(6-chloro-3-pyridinyl)methyl]-

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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-Isoindole-1,3(2H)-dione, 2-[(6-chloro-3-pyridinyl)methyl]-

Clc1ccc(cn1)CN1C(=O)c2c(C1=O)cccc2 Request for Quotation
Chemical Name: 1H-Isoindole-1,3(2H)-dione, 2-[(6-chloro-3-pyridinyl)methyl]-
CAS Number: 120739-60-8
Product Number: AG008ZM1(AGN-PC-0011YT)
Synonyms:
MDL No:
Molecular Formula: C14H9ClN2O2
Molecular Weight: 272.6865

Identification/Properties

Computed Properties
Molecular Weight:
272.688g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
272.035g/mol
Monoisotopic Mass:
272.035g/mol
Topological Polar Surface Area:
50.3A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
364
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, 2-((6-Chloropyridin-3-yl)methyl)isoindoline-1,3-dione serves as a versatile building block with significant applications. This compound, through its unique structural properties, plays a crucial role in the design and synthesis of various organic molecules and pharmaceutical compounds. With its specific functional groups and reactivity, 2-((6-Chloropyridin-3-yl)methyl)isoindoline-1,3-dione can be utilized as a key intermediate in the production of complex molecules, enabling the efficient construction of diverse chemical structures. Its ability to participate in a wide range of synthetic transformations makes it a valuable tool for organic chemists seeking to access novel compounds for research and development purposes.