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Key Documents

W213209

Sigma-Aldrich

Benzoin

≥98%

Synonym(s):

α-Hydroxy-α-phenylacetophenone, α-Hydroxybenzyl phenyl ketone, 2-Hydroxy-2-phenylacetophenone

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About This Item

Linear Formula:
C6H5CH(OH)COC6H5
CAS Number:
Molecular Weight:
212.24
FEMA Number:
2132
Beilstein/REAXYS Number:
391839
EC Number:
Council of Europe no.:
162
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
7.028

biological source

synthetic

grade

Kosher

reg. compliance

FDA 21 CFR 172.515
FDA 21 CFR 73.1

assay

≥98%

bp

194 °C/12 mmHg (lit.)

mp

134-138 °C (lit.)

application(s)

flavors and fragrances

organoleptic

medicinal; vanilla; balsamic

SMILES string

OC(c1ccccc1)C(=O)c2ccccc2

InChI

1S/C14H12O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13,15H

InChI key

ISAOCJYIOMOJEB-UHFFFAOYSA-N

Gene Information

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Other Notes

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Dah-Yuu Lu et al.
Phytomedicine : international journal of phytotherapy and phytopharmacology, 19(12), 1093-1100 (2012-07-24)
Prenyl-phloroglucinol derivatives from hop plants have been shown to have anticancer activities. This study is the first to investigate the anticancer effects of the new phloroglucinol derivative (2,4-bis(4-fluorophenylacetyl)phloroglucinol; BFP). BFP induced cell death and anti-proliferation in three glioma, U251, U87
Wei-Jian Xue et al.
Chemical communications (Cambridge, England), 48(29), 3485-3487 (2012-01-31)
A highly efficient method for the synthesis of oxazole derivatives from methyl ketones, benzoins and ammonium acetate has been established via a novel strategy-convergent integration of two self-labor domino sequences. Owing to the simple and readily available starting materials, mild
Tsuneomi Kawasaki et al.
Angewandte Chemie (International ed. in English), 50(35), 8131-8133 (2011-07-16)
Trigger happy: chiral oxygen isotopomers of hydrobenzoin ([(18)O](R)-1 and [(18)O](S)-1) acted as chiral triggers to induce the enantioselective addition of iPr(2)Zn to pyrimidine-5-carbaldehyde. An extremely small chiral influence arising from the presence of the oxygen isotope ((18)O) is amplified through
S R Jim et al.
Journal of chromatography. A, 1218(40), 7203-7210 (2011-09-09)
Ultrathin-layer chromatography (UTLC) provides the high sensitivities and rapid separations over short distances desirable in many analytical applications. The dependence of these performance benefits on UTLC layer microstructure motivates continued stationary phase engineering efforts. A new method of modifying the
Oldamur Hollóczki et al.
The Journal of organic chemistry, 77(14), 6014-6022 (2012-06-27)
The reaction energy profiles of the benzoin condensation from three aldehydes catalyzed by imidazol-2-ylidene, triazol-3-ylidene, and thiazol-2-ylidene have been investigated computationally. The barriers for all steps of all investigated reactions have been found to be low enough to indicate the

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