1-(furan-2-ylmethyl)-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea


Chemical Name: 1-(furan-2-ylmethyl)-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea
CAS Number: 874297-85-5
Product Number: AG004MGP(AGN-PC-0713DK)
Synonyms:
MDL No:
Molecular Formula: C18H23BN2O4
Molecular Weight: 342.1972

Identification/Properties


Properties
BP:
463.7 °C at 760 mmHg
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
342.202g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
342.175g/mol
Monoisotopic Mass:
342.175g/mol
Topological Polar Surface Area:
72.7A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
462
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-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



N-(2-Furanylmethyl)-N′-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea, commonly referred to as $name$, is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in the preparation of various organic molecules due to its ability to undergo selective reactions and form structurally complex products.In chemical synthesis, $name$ is commonly employed as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its functional groups enable it to participate in diverse chemical transformations, such as coupling reactions, cross-coupling reactions, and substitution reactions. Moreover, the presence of the boron-containing moiety enhances its reactivity and enables selective C–C and C–N bond formation.Furthermore, the furanyl and phenyl groups in $name$ provide additional opportunities for further functionalization, allowing for the introduction of specific chemical functionalities and structural modifications. This versatility makes $name$ a valuable tool for designing and synthesizing complex molecules with desired properties for various applications in the fields of medicinal chemistry, materials science, and organic synthesis.