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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)-

4-((Benzyloxycarbonylamino)methyl)phenylboronic acid

OB(c1ccc(cc1)CNC(=O)OCc1ccccc1)O Request for Quotation
Chemical Name: 4-((Benzyloxycarbonylamino)methyl)phenylboronic acid
CAS Number: 914452-61-2
Product Number: AG00GTE6(AGN-PC-0WA8Z0)
Synonyms:
MDL No:
Molecular Formula: C15H16BNO4
Molecular Weight: 285.1028

Identification/Properties

Computed Properties
Molecular Weight:
285.106g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
6
Exact Mass:
285.117g/mol
Monoisotopic Mass:
285.117g/mol
Topological Polar Surface Area:
78.8A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
313
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of (4-((((Benzyloxy)carbonyl)amino)methyl)phenyl)boronic acid in chemical synthesis lies in its role as a versatile building block for the construction of complex organic molecules. This compound, commonly referred to as $name$, serves as a key intermediate in the formation of various pharmaceuticals, agrochemicals, and materials used in research and industry. Its unique structural features make it an essential component in the development of innovative synthetic strategies, allowing chemists to efficiently access a wide range of structurally diverse compounds. By utilizing $name$ as a chemical reagent, researchers can facilitate the synthesis of target molecules with specific functionalities and properties, advancing the field of organic chemistry and enabling the creation of new materials with tailored characteristics.