CAS 76-84-6|triphenylmethanol|TRIPHENYLCARBINOL|triphenylmethanol|Tritanol|Triphenylmethanol|Triphenylcarbinol|羟基三苯基甲烷|三苯基甲醇|Triphenylmethanol|三苯甲醇|Trityl alcohol|BL 3756|三苯甲醇|Tr...

General Information

Structure

Molecular Formula

C₁₉H₁₆O

Molecular Mass

260.32974

Exact Mass

260.12011513

Charge

InChI

InChI=1S/C19H16O/c20-19(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15,20H

InChIKey

LZTRCELOJRDYMQ-UHFFFAOYSA-N

Canonic Smiles

OC(c1ccccc1)(c1ccccc1)c1ccccc1

Isomeric Smiles

OC(c1ccccc1)(c1ccccc1)c1ccccc1

Calculated Properties

JChem

Acid pKa

12.736887

H Acceptors

H Donor

LogD (pH = 5.5)

4.638378

LogD (pH = 7.4)

4.638376

Log P

4.638378

Molar Refractivity

83.3115

Polarizability

32.05915

Polar Surface Area

20.23

Rotatable Bonds

Lipinski's Rule of Five

true

Data Source

Names and Identifiers

IUPAC name

triphenylmethanol

Synonyms

TRIPHENYLCARBINOLTriphenylmethanolTritanolTriphenylcarbinol三苯基甲醇羟基三苯基甲烷Triphenylmethanol三苯甲醇Trityl alcoholBL 3756Triphenyl carbinolα,α-DiphenylbenzenemethanolNSC 4050三苯甲醇HydroxytriphenylmethaneTrityl AlcoholTriphenylmethanolU 45483Triphenylmethyl Alcohol

IUPAC Traditional name

triphenylmethanol

Names and Identifiers

Registration numbers

CAS Number

EC Number

PubChem CID

Chemspider ID

PubChem SID

1620896862484818924889781

Wikipedia Title

CHEMBL

Beilstein Number

MDL Number

Merck Index

Registration numbers

Properties

Safety Information

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Properties

Related Proteins

No Data Available

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Molecular Spectra

No Data Available

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Molecule Details

MP Biomedicals Rare Chemical collection

Sigma Aldrich

134848

Packaging
50, 250 g in poly bottle

TRC

T808950

A triaryl methane derivative as antiproliferative agent.

Molecule Details

References

PubChem Literature

From Data Sources

• Buchel, K., et al.: Arzneim.-Forsch., 22, 1260 (1972)

• Sawyer, P., et al.: Drugs, 9, 424 (1972)

• Protection of thiols, such as cysteine residues in peptide synthesis, as their S-trityl derivatives can be accomplished in high yield in TFA. Cleavage can be effected with HBr in AcOH: J. Chem. Soc. (C), 2683 (1970), with Hg(II) salts, or by oxidation to the disulfide with I₂ in MeOH: Helv. Chim. Acta, 51, 2061 (1968). See also Appendix 6.

References

Bioactivity

PubChem BioAssay

Bioactivity