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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)-

N-cyclopropyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide

O=C(c1cccc(c1)B1OC(C(O1)(C)C)(C)C)NC1CC1 Request for Quotation
Chemical Name: N-cyclopropyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
CAS Number: 914397-31-2
Product Number: AG006MBB(AGN-PC-01NOTJ)
Synonyms:
MDL No:
Molecular Formula: C16H22BNO3
Molecular Weight: 287.1618

Identification/Properties

Properties
Storage:
2-8℃;Keep in dry area;
Computed Properties
Molecular Weight:
287.166g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
287.169g/mol
Monoisotopic Mass:
287.169g/mol
Topological Polar Surface Area:
47.6A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
404
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

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Chemical Structure


The compound N-Cyclopropyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide has found significant utility in chemical synthesis as a versatile building block. Its strategic incorporation in synthetic pathways has enabled the efficient construction of various complex organic molecules. This compound serves as a valuable tool in the synthesis of diverse pharmaceuticals, agrochemicals, and materials due to its ability to participate in key bond-forming reactions. In particular, its cyclopropyl group provides unique reactivity, offering opportunities for stereochemical control and molecular diversity in target molecule design. Furthermore, the boron-containing moiety plays a pivotal role in cross-coupling reactions, enabling the rapid assembly of intricate molecular structures. Through its strategic utilization in chemical synthesis, N-Cyclopropyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide contributes to the advancement of synthetic methodology and the creation of novel compounds with diverse applications.