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4-Benzyloxybenzylalkohol
97%
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About This Item
Lineare Formel:
C6H5CH2OC6H4CH2OH
CAS-Nummer:
Molekulargewicht:
214.26
Beilstein:
1877819
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
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Assay
97%
Form
solid
mp (Schmelzpunkt)
86-87 °C (lit.)
Funktionelle Gruppe
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
InChIKey
OEBIVOHKFYSBPE-UHFFFAOYSA-N
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Anwendung
4-Benzyloxybenzyl alcohol was used in the synthesis of:
- 13C-labelled derivatives of the isoflavonoid phytoestrogens, genistein, biochanin A, daidzein and formononetin
- benzyl4-(tert-butyldiphenylsiloxy-M1-carbamoyloxymethyl)phenylether
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Gloves, type N95 (US)
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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
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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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