Boronic acid, [4-[[(phenylmethyl)amino]carbonyl]phenyl]-|252663-47-1,AngeneChemical

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

Boronic acid, [4-[[(phenylmethyl)amino]carbonyl]phenyl]-

Request for Quotation

Chemical Name:	Boronic acid, [4-[[(phenylmethyl)amino]carbonyl]phenyl]-
CAS Number:	252663-47-1
Product Number:	AG003AAP(AGN-PC-0KKVAJ)
Synonyms:
MDL No:	MFCD03411953
Molecular Formula:	C14H14BNO3
Molecular Weight:	255.0769

Identification/Properties
Safety Information
NMR Spectrum
Other Analytical Data
Customer Feedback

Identification/Properties

Computed Properties

Molecular Weight:

255.08g/mol

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

255.107g/mol

Monoisotopic Mass:

255.107g/mol

Topological Polar Surface Area:

69.6A^2

Heavy Atom Count:

Formal Charge:

Complexity:

284

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

Compound Is Canonicalized:

Yes

Safety Information

GHS Pictogram:

Signal Word:

Warning

UN#:

Hazard Statements:

H315-H319-H335

Precautionary Statements:

P261-P305+P351+P338

Class:

Packing Group:

NMR Spectrum

Other Analytical Data

Request for Quotation

Quantity Required:*

Company Name:

Contact Person:*

Email:*

Tel:*

Country:*

Others:(Optional)

Verification Code:

Customer Feedback

Chemical Structure

4-(N-Benzylaminocarbonyl)phenylboronic acid, also known as $name$, is a versatile compound commonly used in chemical synthesis. Due to its unique structure, $name$ is utilized as a key building block in the synthesis of various organic molecules. In particular, this compound is valued for its ability to react with a wide range of electrophiles, such as alkyl halides and epoxides, to form C-C and C-N bonds.One important application of $name$ in chemical synthesis is in the formation of biaryl compounds. By combining $name$ with aryl halides or pseudo-halides in the presence of palladium catalysts, chemists can efficiently access structurally diverse biaryl molecules. These biaryl compounds are prevalent in pharmaceuticals, agrochemicals, and materials science, making the synthetic route involving $name$ of great interest to researchers in these fields.Additionally, $name$ plays a crucial role in Suzuki-Miyaura cross-coupling reactions, a powerful tool in organic synthesis. In this reaction, the boronic acid functionality of $name$ undergoes transmetallation with a palladium catalyst, allowing for the formation of carbon-carbon bonds between two distinct aryl groups. This process enables the construction of complex molecules with high efficiency and selectivity, further highlighting the utility of $name$ in chemical synthesis.