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187372

Sigma-Aldrich

4-Benzyloxybenzyl alcohol

97%

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About This Item

Linear Formula:
C6H5CH2OC6H4CH2OH
CAS Number:
Molecular Weight:
214.26
Beilstein/REAXYS Number:
1877819
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

97%

form

solid

mp

86-87 °C (lit.)

functional group

hydroxyl
phenyl

SMILES string

OCc1ccc(OCc2ccccc2)cc1

InChI

1S/C14H14O2/c15-10-12-6-8-14(9-7-12)16-11-13-4-2-1-3-5-13/h1-9,15H,10-11H2

InChI key

OEBIVOHKFYSBPE-UHFFFAOYSA-N

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Application

4-Benzyloxybenzyl alcohol was used in the synthesis of:
  • 13C-labelled derivatives of the isoflavonoid phytoestrogens, genistein, biochanin A, daidzein and formononetin[1]
  • benzyl4-(tert-butyldiphenylsiloxy-M1-carbamoyloxymethyl)phenylether[2]

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Federica Tonolo et al.
Antioxidants (Basel, Switzerland), 9(2) (2020-02-06)
Due to their beneficial properties, fermented foods are considered important constituents of the human diet. They also contain bioactive peptides, health-promoting compounds studied for a wide range of effects. In this work, several antioxidant peptides extracted from fermented milk proteins
The synthesis of precisely structured polyurethanes. Part 2. Chain building methodology.
George MH, et al.
Journal of the Chemical Society. Perkin Transactions 1, 12, 1395-1401 (1996)
Synthesis of [4-13C]-Isoflavonoid Phytoestrogens.
Whalley JL, et al.
Tetrahedron, 56(3), 455-460 (2000)
Alexandre Murza et al.
Organic & biomolecular chemistry, 15(2), 449-458 (2016-12-08)
Apelin is the endogenous ligand for the G protein-coupled receptor APJ and exerts a key role in regulating cardiovascular functions. We report herein a novel series of macrocyclic analogues of apelin-13 in which the N- and C-terminal residues as well
Armine Avetisyan et al.
Neurochemistry international, 140, 104799-104799 (2020-08-14)
The receptor for advanced glycation end products (RAGE) is considered to contribute to the pathogenesis of Alzheimer's disease (AD), mediating amyloid beta (Aβ) accumulation, mitochondrial damage, and neuroinflammation. Previously, we have synthesized small peptides corresponding to the fragments (60-76) (P1)

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