CAS 148-86-7
:[1,1′-Biphenyl]-4-ol, 4-acetate
Description:
[1,1′-Biphenyl]-4-ol, 4-acetate, also known as 4-Acetoxy-1,1'-biphenyl, is an organic compound characterized by its biphenyl structure with an acetoxy functional group at the para position relative to the hydroxyl group. This compound typically appears as a white to off-white solid and is soluble in organic solvents such as ethanol and ether, but has limited solubility in water. It exhibits properties typical of phenolic compounds, including potential antioxidant activity and reactivity in electrophilic substitution reactions. The presence of the acetoxy group enhances its stability and alters its reactivity compared to unsubstituted biphenyl derivatives. This compound is often utilized in organic synthesis and may serve as an intermediate in the production of various pharmaceuticals and agrochemicals. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Overall, [1,1′-Biphenyl]-4-ol, 4-acetate is a versatile compound with applications in both research and industrial settings.
Formula:C14H12O2
InChI:InChI=1S/C14H12O2/c1-11(15)16-14-9-7-13(8-10-14)12-5-3-2-4-6-12/h2-10H,1H3
InChI key:InChIKey=MISFQCBPASYYGV-UHFFFAOYSA-N
SMILES:O(C(C)=O)C1=CC=C(C=C1)C2=CC=CC=C2
Synonyms:- (4-Phenylphenyl) acetate
- 1,1'-Biphenyl-4-Ol Acetate
- 4-Acetoxy-1,1′-biphenyl
- 4-Biphenyl Acetate
- 4-Biphenylol, acetate
- 4-Biphenylyl Acetate
- 4-Phenylphenol Acetate
- Acetic Acid 4-Biphenyl Ester
- Biphenyl-4-Yl Acetate
- NSC 404087
- Phenol, p-phenyl-, acetate
- Timtec-Bb Sbb008322
- [1,1′-Biphenyl]-4-ol, 4-acetate
- [1,1′-Biphenyl]-4-yl acetate
- p-Biphenol acetate.
- p-Phenylphenol acetate
- p-Phenylphenyl acetate
- 4-ACETOXYBIPHENYL
- See more synonyms
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Found 5 products.
4-Acetoxybiphenyl
CAS:Formula:C14H12O2Purity:>99.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:212.254-Acetoxybiphenyl
CAS:<p>4-Acetoxybiphenyl is a biphenyl that can be solubilized in water and has a viscosity of about 20 to 100 cps. It reacts with benzoate in the presence of acid catalyst to produce phenyl groups. 4-Acetoxybiphenyl has been shown to inhibit peptide binding, which may lead to protein degradation, and also have a strong reaction with chloride ions. 4-Acetoxybiphenyl is not active against tissues and its metabolic product profile is not well characterized.</p>Formula:C14H12O2Purity:Min. 95%Color and Shape:PowderMolecular weight:212.24 g/mol




