1. Home
  2. 1H-Imidazole, 4,5-dibromo-1-(triphenylmethyl)-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-Imidazole, 4,5-dibromo-1-(triphenylmethyl)-

Brc1ncn(c1Br)C(c1ccccc1)(c1ccccc1)c1ccccc1 Request for Quotation
Chemical Name: 1H-Imidazole, 4,5-dibromo-1-(triphenylmethyl)-
CAS Number: 112517-23-4
Product Number: AG003KH9(AGN-PC-0NL6MG)
Synonyms:
MDL No:
Molecular Formula: C22H16Br2N2
Molecular Weight: 468.1838

Identification/Properties

Properties
MP:
223-225 °C
BP:
533.4°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
468.192g/mol
XLogP3:
6.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
4
Exact Mass:
467.966g/mol
Monoisotopic Mass:
465.968g/mol
Topological Polar Surface Area:
17.8A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
394
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

Request for Quotation

Customer Feedback

Chemical Structure


When it comes to chemical synthesis, 4,5-Dibromo-1-trityl-1H-imidazole plays a crucial role as a versatile building block. This compound serves as a valuable reagent in various synthetic pathways, enabling the creation of intricate molecular structures with precision and efficiency. In the realm of organic chemistry, 4,5-Dibromo-1-trityl-1H-imidazole is utilized for its ability to facilitate the formation of carbon-carbon and carbon-nitrogen bonds, making it an essential component in the synthesis of complex organic molecules. Its unique structural characteristics make it particularly well-suited for the modification of functional groups and the construction of diverse chemical frameworks. Additionally, this compound exhibits excellent compatibility with a wide range of reaction conditions, making it a versatile tool for chemists seeking to tailor-make compounds for specific applications. By incorporating 4,5-Dibromo-1-trityl-1H-imidazole into synthetic strategies, researchers can enhance the efficiency and precision of their chemical transformations, ultimately leading to the development of novel compounds with tailored properties and functionalities.