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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)-

3-(2,3-dihydro-1,4-benzodioxin-6-yl)-1H-pyrazole-4-carbaldehyde

O=Cc1cn[nH]c1c1ccc2c(c1)OCCO2 Request for Quotation
Chemical Name: 3-(2,3-dihydro-1,4-benzodioxin-6-yl)-1H-pyrazole-4-carbaldehyde
CAS Number: 1006482-46-7
Product Number: AG00H9A9(AGN-PC-0WAGG1)
Synonyms:
MDL No:
Molecular Formula: C12H10N2O3
Molecular Weight: 230.2194

Identification/Properties

Computed Properties
Molecular Weight:
230.223g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
230.069g/mol
Monoisotopic Mass:
230.069g/mol
Topological Polar Surface Area:
64.2A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
287
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


5-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)-1H-pyrazole-4-carbaldehyde is a versatile compound widely used in chemical synthesis due to its unique structural properties. As a key building block in organic chemistry, this compound plays a crucial role in the development of various pharmaceuticals, agrochemicals, and materials.Its functional groups allow for efficient derivatization and modification, making it a valuable intermediate in the synthesis of complex molecules. Specifically, 5-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)-1H-pyrazole-4-carbaldehyde is utilized in the formation of heterocyclic compounds and biologically active molecules.Furthermore, the presence of the aldehyde group enables selective reactions for further functionalization, facilitating the creation of diverse chemical entities with specific properties. Its strategic placement within the molecule enhances its utility as a synthetic tool for the construction of intricate molecular frameworks.Overall, 5-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)-1H-pyrazole-4-carbaldehyde is an indispensable component in the toolbox of synthetic chemists, enabling the efficient and precise synthesis of a wide range of valuable compounds with diverse applications.