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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)-

2H-1-Benzopyran-3-carboxaldehyde, 7-methoxy-

O=CC1=Cc2c(OC1)cc(cc2)OC Request for Quotation
Chemical Name: 2H-1-Benzopyran-3-carboxaldehyde, 7-methoxy-
CAS Number: 57543-39-2
Product Number: AG00EAU6(AGN-PC-0JKSPH)
Synonyms:
MDL No:
Molecular Formula: C11H10O3
Molecular Weight: 190.1953

Identification/Properties

Computed Properties
Molecular Weight:
190.198g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
190.063g/mol
Monoisotopic Mass:
190.063g/mol
Topological Polar Surface Area:
35.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
247
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


7-Methoxy-2H-chromene-3-carbaldehyde, also known as $name$, is a versatile compound widely utilized in chemical synthesis. With its unique structure and reactivity, this aldehyde derivative plays a crucial role in the creation of various chemical compounds through its involvement in multiple key reactions.In organic synthesis, 7-Methoxy-2H-chromene-3-carbaldehyde serves as a valuable building block in the formation of heterocyclic compounds, particularly in the construction of chromene derivatives. Its aldehyde group allows for selective functionalization reactions, enabling the introduction of desired substituents to tailor the properties of the final product.Furthermore, the presence of the methoxy group in the molecule enhances its compatibility in cross-coupling reactions and C-H activation processes, leading to efficient derivatization and modification of the molecular structure. This compound's diverse reactivity makes it a valuable tool in the development of novel pharmaceuticals, agrochemicals, and materials with specific functional properties.In summary, the application of 7-Methoxy-2H-chromene-3-carbaldehyde in chemical synthesis extends from its role as a key intermediate to its potential in the creation of complex molecular frameworks with tailored functionalities. Its versatility and compatibility in various synthetic routes make it a valuable asset in the hands of researchers and chemists striving to innovate and advance the field of organic chemistry.