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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)-

Boronic acid, [3-[(1,1-dimethylethoxy)methyl]phenyl]-

OB(c1cccc(c1)COC(C)(C)C)O Request for Quotation
Chemical Name: Boronic acid, [3-[(1,1-dimethylethoxy)methyl]phenyl]-
CAS Number: 858364-78-0
Product Number: AG004RBA(AGN-PC-0KZVAS)
Synonyms:
MDL No:
Molecular Formula: C11H17BO3
Molecular Weight: 208.0619

Identification/Properties

Properties
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
208.064g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
208.127g/mol
Monoisotopic Mass:
208.127g/mol
Topological Polar Surface Area:
49.7A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
189
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
Precautionary Statements:
P264-P270-P301+P312+P330-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(3-(tert-Butoxymethyl)phenyl)boronic acid is a versatile compound widely used in chemical synthesis as a key building block in organic reactions. Its unique structure containing a boronic acid group enables it to participate in various synthetic transformations, particularly in Suzuki-Miyaura cross-coupling reactions.This compound serves as a valuable reagent for the formation of carbon-carbon bonds, allowing for the construction of complex organic molecules. By reacting with aryl halides or triflates in the presence of a palladium catalyst, (3-(tert-Butoxymethyl)phenyl)boronic acid can undergo coupling reactions to create biaryl compounds with high regioselectivity and yield.Additionally, (3-(tert-Butoxymethyl)phenyl)boronic acid has found applications in the synthesis of pharmaceuticals, agrochemicals, and advanced materials due to its role in creating structurally diverse and biologically active molecules. Its compatibility with a variety of functional groups and its relatively mild reaction conditions make it a valuable tool in the hands of synthetic chemists aiming to access a wide range of chemical structures.In summary, the utility of (3-(tert-Butoxymethyl)phenyl)boronic acid in chemical synthesis lies in its ability to facilitate the construction of complex organic molecules through Suzuki-Miyaura cross-coupling reactions, making it an essential reagent for the preparation of diverse compounds in various fields of chemistry.