123714
4-(Benzyloxy)benzaldehyde
97%
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About This Item
Linear Formula:
C6H5CH2OC6H4CHO
CAS Number:
Molecular Weight:
212.24
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-527-2
Beilstein/REAXYS Number:
1242385
MDL number:
Product Name
4-(Benzyloxy)benzaldehyde, 97%
InChI key
ZVTWZSXLLMNMQC-UHFFFAOYSA-N
InChI
1S/C14H12O2/c15-10-12-6-8-14(9-7-12)16-11-13-4-2-1-3-5-13/h1-10H,11H2
SMILES string
[H]C(=O)c1ccc(OCc2ccccc2)cc1
assay
97%
mp
71-74 °C (lit.)
functional group
aldehyde
phenyl
Quality Level
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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
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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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