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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)-

[1-[(2-methylpropan-2-yl)oxycarbonyl]-5-[(2-methylpropan-2-yl)oxycarbonylamino]indol-2-yl]boronic acid

O=C(OC(C)(C)C)Nc1ccc2c(c1)cc(n2C(=O)OC(C)(C)C)B(O)O Request for Quotation
Chemical Name: [1-[(2-methylpropan-2-yl)oxycarbonyl]-5-[(2-methylpropan-2-yl)oxycarbonylamino]indol-2-yl]boronic acid
CAS Number: 913388-66-6
Product Number: AG006NRZ(AGN-PC-0BSCPU)
Synonyms:
MDL No:
Molecular Formula: C18H25BN2O6
Molecular Weight: 376.2119

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Computed Properties
Molecular Weight:
376.216g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
6
Exact Mass:
376.181g/mol
Monoisotopic Mass:
376.181g/mol
Topological Polar Surface Area:
110A^2
Heavy Atom Count:
27
Formal Charge:
0
Complexity:
557
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#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound $name$ is a versatile building block employed in chemical synthesis for its unique reactivity and functional groups. In particular, (1-(tert-Butoxycarbonyl)-5-((tert-butoxycarbonyl)amino)-1H-indol-2-yl)boronic acid is utilized as a key intermediate in organic reactions, serving as a valuable tool in the construction of complex molecular structures. Its boronic acid functionality enables it to participate in various coupling reactions, such as Suzuki-Miyaura cross-coupling, allowing for the formation of carbon-carbon bonds. This enables the efficient synthesis of biologically active molecules, pharmaceuticals, and advanced materials. Additionally, the presence of the t-Boc protecting groups enhances the compound's stability and compatibility in synthetic pathways, making it an essential component in the toolbox of synthetic chemists.