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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-Pyrazole, 4-bromo-1-(triphenylmethyl)-

Brc1cnn(c1)C(c1ccccc1)(c1ccccc1)c1ccccc1 Request for Quotation
Chemical Name: 1H-Pyrazole, 4-bromo-1-(triphenylmethyl)-
CAS Number: 95162-14-4
Product Number: AG003KV4(AGN-PC-0NBCP4)
Synonyms:
MDL No: MFCD09907863
Molecular Formula: C22H17BrN2
Molecular Weight: 389.2878

Identification/Properties

Properties
MP:
186-188℃ (hexane )
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
389.296g/mol
XLogP3:
5.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
4
Exact Mass:
388.058g/mol
Monoisotopic Mass:
388.058g/mol
Topological Polar Surface Area:
17.8A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
363
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Bromo-1-tritylpyrazole is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. This compound serves as a valuable building block in the preparation of various organic molecules and pharmaceutical compounds. Its bromo and trityl functional groups enable selective and efficient derivatization reactions, making it a valuable tool in the synthesis of complex organic structures. Additionally, 4-Bromo-1-tritylpyrazole exhibits excellent stability under a wide range of reaction conditions, making it a reliable reagent for diverse synthetic applications. Its compatibility with a variety of reaction conditions and substrates makes it a valuable asset for chemists seeking to streamline their synthetic pathways and optimize their processes. Whether used as a key intermediate or as a versatile reagent in multistep syntheses, 4-Bromo-1-tritylpyrazole offers chemists a powerful tool for achieving their synthetic goals.