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Merck

187372

Sigma-Aldrich

4-苯甲氧基苯甲醇

97%

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About This Item

线性分子式:
C6H5CH2OC6H4CH2OH
CAS号:
分子量:
214.26
Beilstein:
1877819
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

97%

形狀

solid

mp

86-87 °C (lit.)

官能基

hydroxyl
phenyl

SMILES 字串

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 密鑰

OEBIVOHKFYSBPE-UHFFFAOYSA-N

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應用

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]

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
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
Synthesis of [4-13C]-Isoflavonoid Phytoestrogens.
Whalley JL, et al.
Tetrahedron, 56(3), 455-460 (2000)
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)
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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