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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)-

Benzoic acid,p-borono-, 1-propyl ester (7CI)

CCCOC(=O)c1ccc(cc1)B(O)O Request for Quotation
Chemical Name: Benzoic acid,p-borono-, 1-propyl ester (7CI)
CAS Number: 91062-38-3
Product Number: AG006F0H(AGN-PC-0VRLOJ)
Synonyms:
MDL No:
Molecular Formula: C10H13BO4
Molecular Weight: 208.0188

Identification/Properties

Properties
MP:
108-112 °C
BP:
366.42°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
208.02g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
208.091g/mol
Monoisotopic Mass:
208.091g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
200
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#:
-
Hazard Statements:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Propoxycarbonyl)phenylboronic acid, a versatile organic compound, plays a crucial role in chemical synthesis as a valuable building block in the creation of various organic molecules. This compound is commonly utilized in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid derivative to facilitate the formation of carbon-carbon bonds.In the realm of organic chemistry, the application of 4-(Propoxycarbonyl)phenylboronic acid enables the introduction of the phenyl group into target molecules, thereby broadening the scope of potential organic compounds that can be synthesized. Its functional group allows for selective reactions with other organic molecules, leading to the development of complex structures with specific functionalities.Furthermore, the use of 4-(Propoxycarbonyl)phenylboronic acid in chemical synthesis offers chemists a reliable method for constructing biaryl compounds, which are prevalent in numerous pharmaceuticals, agrochemicals, and materials science applications. By harnessing the unique reactivity of this compound, researchers can access a diverse array of molecular structures with tailored properties, laying the groundwork for advancements in various scientific fields.