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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)-

Phenol, 4-(triphenylmethyl)-

Oc1ccc(cc1)C(c1ccccc1)(c1ccccc1)c1ccccc1 Request for Quotation
Chemical Name: Phenol, 4-(triphenylmethyl)-
CAS Number: 978-86-9
Product Number: AG00345O(AGN-PC-0JL9ON)
Synonyms:
MDL No:
Molecular Formula: C25H20O
Molecular Weight: 336.4257

Identification/Properties

Properties
MP:
283-286 °C(lit.)
BP:
432.9°C (rough estimate)
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.6380 (estimate)
Computed Properties
Molecular Weight:
336.434g/mol
XLogP3:
6.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
4
Exact Mass:
336.151g/mol
Monoisotopic Mass:
336.151g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
358
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-Tritylphenol is a versatile compound commonly utilized in chemical synthesis as a protecting group for alcohols. This compound plays a crucial role in organic chemistry by temporarily masking the hydroxyl functional group of alcohols to prevent unwanted reactions or to control regioselectivity during various transformations. Additionally, 4-Tritylphenol can be selectively removed under specific conditions, allowing the liberated alcohol to participate in subsequent reactions, making it a valuable tool in multi-step synthesis strategies. This compound's ability to facilitate the manipulation of alcohol functionalities with precision and efficiency makes it an indispensable building block in the synthesis of complex organic molecules.