1. Home
  2. [3-(cyclohexyloxymethyl)phenyl]boronic acid

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-(cyclohexyloxymethyl)phenyl]boronic acid

OB(c1cccc(c1)COC1CCCCC1)O Request for Quotation
Chemical Name: [3-(cyclohexyloxymethyl)phenyl]boronic acid
CAS Number: 1256358-64-1
Product Number: AG000O5J(AGN-PC-09PV7F)
Synonyms:
MDL No:
Molecular Formula: C13H19BO3
Molecular Weight: 234.0992

Identification/Properties

Computed Properties
Molecular Weight:
234.102g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
234.143g/mol
Monoisotopic Mass:
234.143g/mol
Topological Polar Surface Area:
49.7A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
217
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The compound (3-((Cyclohexyloxy)methyl)phenyl)boronic acid, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. It is commonly used in organic chemistry for the formation of carbon-carbon (C-C) and carbon-heteroatom bonds through Suzuki-Miyaura cross-coupling reactions.This boronic acid derivative is particularly valued for its ability to react with various electrophiles such as aryl halides, triflates, and mesylates under mild reaction conditions. The resulting products exhibit a wide range of applications in pharmaceuticals, agrochemicals, materials science, and other industrial sectors.$name$ offers chemists a powerful tool for the selective introduction of the (3-((Cyclohexyloxy)methyl)phenyl) group into complex molecules, enabling the synthesis of new, biologically active compounds or functional materials with tailored properties. Its stability and compatibility with diverse reaction conditions make it a valuable reagent for the construction of intricate molecular architectures in organic synthesis.