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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)-

1H-Pyrrole, 3,4-dibromo-1-[tris(1-methylethyl)silyl]-

CC([Si](n1cc(c(c1)Br)Br)(C(C)C)C(C)C)C Request for Quotation
Chemical Name: 1H-Pyrrole, 3,4-dibromo-1-[tris(1-methylethyl)silyl]-
CAS Number: 93362-54-0
Product Number: AG0063QX(AGN-PC-0NGRG6)
Synonyms:
MDL No:
Molecular Formula: C13H23Br2NSi
Molecular Weight: 381.2219

Identification/Properties

Properties
BP:
325.2°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
381.227g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
4
Exact Mass:
380.995g/mol
Monoisotopic Mass:
378.997g/mol
Topological Polar Surface Area:
4.9A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
224
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,4-Dibromo-1-(triisopropylsilyl)-1H-pyrrole is a versatile compound commonly used in chemical synthesis as a key building block for creating complex organic molecules. This compound acts as a powerful reagent in multiple reactions, including but not limited to Suzuki-Miyaura coupling, Heck reactions, and Sonogashira coupling. Its unique structure allows for selective functionalization at different positions, enabling chemists to precisely control the formation of specific bonds in the target molecule. Furthermore, the triisopropylsilyl group serves as a protecting group, safeguarding certain functional groups from unwanted reactions during the synthesis process. Overall, this compound plays a crucial role in the efficient and strategic assembly of advanced organic compounds in the realm of chemical synthesis.