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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(3H)-Isobenzofuranone, 4-chloro-

O=C1OCc2c1cccc2Cl Request for Quotation
Chemical Name: 1(3H)-Isobenzofuranone, 4-chloro-
CAS Number: 52010-22-7
Product Number: AG003L89(AGN-PC-0KO9PC)
Synonyms:
MDL No: MFCD01718133
Molecular Formula: C8H5ClO2
Molecular Weight: 168.5771

Identification/Properties

Properties
BP:
360.6°C/760mmHg
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
168.576g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
167.998g/mol
Monoisotopic Mass:
167.998g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
181
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


4-Chlorophthalide, often utilized in chemical synthesis, serves as a critical building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials. As a versatile compound, it facilitates the development of innovative molecules through its ability to undergo multiple functionalization reactions. With its chlorine atom strategically positioned within the phthalide structure, 4-Chlorophthalide allows for precise modifications that can enhance the desired properties of the final products. From drug discovery to material science, this compound plays a vital role in enabling the synthesis of diverse compounds with tailored functionalities and applications.