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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)-

4H-1-Benzopyran-4-one, 7-chloro-2,3-dihydro-

Clc1ccc2c(c1)OCCC2=O Request for Quotation
Chemical Name: 4H-1-Benzopyran-4-one, 7-chloro-2,3-dihydro-
CAS Number: 18385-72-3
Product Number: AG0039QS(AGN-PC-001AOZ)
Synonyms:
MDL No:
Molecular Formula: C9H7ClO2
Molecular Weight: 182.6037

Identification/Properties

Computed Properties
Molecular Weight:
182.603g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
182.013g/mol
Monoisotopic Mass:
182.013g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
193
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


7-Chloro-4-chromanone, also known as 7-chloro-4H-chromen-4-one, is a key intermediate in chemical synthesis with versatile applications. This compound serves as a valuable building block in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure makes it a crucial starting material for the synthesis of various heterocyclic compounds.In chemical synthesis, 7-Chloro-4-chromanone is commonly used as a precursor in the preparation of biologically active molecules and pharmacological agents. Its reactivity allows for the introduction of various functional groups through selective chemical reactions, enabling the creation of complex molecular structures. Additionally, this compound can undergo further modifications to generate libraries of compounds for drug discovery and development processes.Moreover, 7-Chloro-4-chromanone plays a significant role in the development of new materials and chemical entities. Its use in organic synthesis facilitates the creation of innovative compounds with diverse properties and applications. By utilizing this intermediate in strategic synthetic pathways, chemists can access novel molecules with enhanced functionalities and potential biological activities.Overall, the versatile nature of 7-Chloro-4-chromanone makes it a valuable tool in chemical synthesis, enabling the efficient and controlled construction of complex molecules for various scientific and industrial purposes.