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  2. 1,2,5-trimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrrole

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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)-

1,2,5-trimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrrole

Cn1c(C)cc(c1C)B1OC(C(O1)(C)C)(C)C Request for Quotation
Chemical Name: 1,2,5-trimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrrole
CAS Number: 1256359-32-6
Product Number: AG000O75(AGN-PC-09PZL2)
Synonyms:
MDL No:
Molecular Formula: C13H22BNO2
Molecular Weight: 235.1303

Identification/Properties

Computed Properties
Molecular Weight:
235.134g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
235.174g/mol
Monoisotopic Mass:
235.174g/mol
Topological Polar Surface Area:
23.4A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
290
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 application of 1,2,5-Trimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole in chemical synthesis involves its utility as a versatile building block for the creation of complex organic molecules. This compound serves as a valuable reagent in the synthesis of various functional materials, pharmaceutical intermediates, and bioactive compounds. Its unique structure and reactivity make it a key component in the development of new chemical entities through diverse synthetic pathways. In particular, its incorporation into molecular frameworks allows for the introduction of specific functional groups and stereochemical control, enabling chemists to access innovative structures with tailored properties. By leveraging the strategic placement of the pyrrole and boron functionalities, researchers can efficiently construct intricate molecular architectures with high regio- and stereoselectivity, advancing the frontier of chemical synthesis.