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123714

Sigma-Aldrich

4-(Benzyloxy)benzaldehyde

97%

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About This Item

Linear Formula:
C6H5CH2OC6H4CHO
CAS Number:
Molecular Weight:
212.24
Beilstein:
1242385
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

mp

71-74 °C (lit.)

functional group

aldehyde
phenyl

SMILES string

[H]C(=O)c1ccc(OCc2ccccc2)cc1

InChI

1S/C14H12O2/c15-10-12-6-8-14(9-7-12)16-11-13-4-2-1-3-5-13/h1-10H,11H2

InChI key

ZVTWZSXLLMNMQC-UHFFFAOYSA-N

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General description

4-(Benzyloxy)benzaldehyde was used in the synthesis of (5-fluoro-(2R*,3S*)-2,3-bis(4-hydroxyphenyl)pentanenitrile),an estrogen receptor β-selective ligand.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Jeongsoo Yoo et al.
Journal of medicinal chemistry, 48(20), 6366-6378 (2005-09-30)
Estrogen receptor beta (ERbeta), a less active ER subtype that appears to have a restraining effect on the more active ERalpha, could be a factor that determines the level of estrogen action in certain estrogen target tissues. ERbeta is found
Oriol Penon et al.
Journal of colloid and interface science, 462, 154-165 (2015-10-12)
The preparation of novel porphyrin derivatives and their immobilization onto iron oxide nanoparticles to build up suitable nanotools for potential use in photodynamic therapy (PDT) has been explored. To achieve this purpose, a zinc porphyrin derivative, ZnPR-COOH, has been synthesized

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