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Merck
모든 사진(1)

주요 문서

187372

Sigma-Aldrich

4-Benzyloxybenzyl alcohol

97%

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About This Item

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

분석

97%

양식

solid

mp

86-87 °C (lit.)

작용기

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

유사한 제품을 찾으십니까? 방문 제품 비교 안내

애플리케이션

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


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문서 라이브러리 방문

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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