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13761

Sigma-Aldrich

2-Benzylphenol

≥98.0% (GC)

Sinônimo(s):

α-Phenyl-o-cresol, 2-Hydroxydiphenylmethane

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About This Item

Fórmula linear:
C6H5CH2C6H4OH
Número CAS:
28994-41-4
Peso molecular:
184.23
Beilstein:
2045725
Número CE:
249-361-8
Número MDL:
MFCD00002242
Código UNSPSC:
12352100
ID de substância PubChem:
57647115
NACRES:
NA.22

Ensaio

≥98.0% (GC)

Formulário

solid

p.e.

312 °C (lit.)

pf

49-51 °C (lit.)
49-51 °C

solubilidade

methanol: soluble 1 g/10 mL, clear, almost colorless

grupo funcional

phenyl

cadeia de caracteres SMILES

Oc1ccccc1Cc2ccccc2

InChI

1S/C13H12O/c14-13-9-5-4-8-12(13)10-11-6-2-1-3-7-11/h1-9,14H,10H2

chave InChI

CDMGNVWZXRKJNS-UHFFFAOYSA-N

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Aplicação

2-Benzylphenol was used as starting reagent in the synthesis of 2-benzylacetate. It was also used in the the synthesis of 6- and 8-benzyl derivatives of 2-(dialkylamino)chromones.

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H319,H335

Classificações de perigo

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análise (COA)

Lot/Batch Number
BCCF7919
338593/1

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Masateru Ono et al.
Chemical & pharmaceutical bulletin, 50(10), 1416-1417 (2002-10-10)
A new ortho-benzoyloxyphenyl acetic acid ester, called vaccihein A (1), was isolated from the fruit of rabbiteye blueberry (Vaccinium ashei). The chemical structure was determined on the basis of spectroscopic data. Compound 1 had antioxidative activity using the ferric thiocyanate
A Balbi et al.
Il Farmaco; edizione scientifica, 37(9), 582-596 (1982-09-01)
Some 2-(dialkylamino)chromones phenyl substituted in position 6 or 7 or 8 were synthesized by reaction of N,N-dialkylethoxycarbonylacetamides with 4- or 3- or 2-biphenylol, respectively, in the presence of phosphorus oxychloride. The pharmacological activity of these compounds was then evaluated and
Yu-Zhe Chen et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 8(7), 916-925 (2009-07-08)
Photo-Fries rearrangements and associated photoreactions of four o-cresyl acylates were investigated in cyclohexane and in unstretched and stretched polyethylene (PE) films with different degrees of crystallinity. The esters differ in the number of phenyl substituents attached to the methyl group
A W Stocklinski
Xenobiotica; the fate of foreign compounds in biological systems, 11(6), 425-432 (1981-06-01)
1. Urine and faeces, and two-hour bile samples from adult male rats dosed with [14C]diphenylmethane were analysed for benzhydrol and 2- and 4-hydroxydiphenyl-methane by silica gel GF t.l.c. and 14C-determination. 2. Mean values of 48.4% and 17.7% of the administered

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