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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)-

[7-methoxycarbonyl-1-[(2-methylpropan-2-yl)oxycarbonyl]indol-2-yl]boronic acid

COC(=O)c1cccc2c1n(C(=O)OC(C)(C)C)c(c2)B(O)O Request for Quotation
Chemical Name: [7-methoxycarbonyl-1-[(2-methylpropan-2-yl)oxycarbonyl]indol-2-yl]boronic acid
CAS Number: 953411-05-7
Product Number: AG003BEH(AGN-PC-07XU6H)
Synonyms:
MDL No:
Molecular Formula: C15H18BNO6
Molecular Weight: 319.1175

Identification/Properties

Properties
Storage:
-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
319.12g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
5
Exact Mass:
319.123g/mol
Monoisotopic Mass:
319.123g/mol
Topological Polar Surface Area:
98A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
463
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:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(1,1-Dimethylethyl) 7-methyl 2-borono-1H-indole-1,7-dicarboxylate, often referred to simply as $name$, is a versatile compound widely used in chemical synthesis. Its unique structure and properties make it a valuable tool in the creation of various organic molecules.One key application of $name$ in chemical synthesis is as a boron-containing reagent for Suzuki-Miyaura cross-coupling reactions. This powerful and widely used reaction allows for the selective formation of carbon-carbon bonds, enabling the construction of complex organic compounds with high efficiency.By serving as a boron source in the Suzuki-Miyaura reaction, 1-(1,1-Dimethylethyl) 7-methyl 2-borono-1H-indole-1,7-dicarboxylate facilitates the coupling of aryl or vinyl boronic acids with aryl or vinyl halides or triflates. This process is essential in the synthesis of pharmaceuticals, agrochemicals, materials science, and various other fields where creating specific carbon-carbon bonds is a crucial step.In summary, $name$ plays a vital role in modern chemical synthesis methods, particularly in the context of Suzuki-Miyaura cross-coupling reactions, enabling chemists to access diverse and valuable organic molecules with precision and efficiency.