513032
4-Benzyloxybromobenzene
96%
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About This Item
Linear Formula:
C6H5CH2OC6H4Br
CAS Number:
Molecular Weight:
263.13
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
96%
Quality Level
assay
96%
bp
166-167 °C/4 mmHg (lit.)
mp
60-63 °C (lit.)
functional group
bromo, phenyl
SMILES string
Brc1ccc(OCc2ccccc2)cc1
InChI
1S/C13H11BrO/c14-12-6-8-13(9-7-12)15-10-11-4-2-1-3-5-11/h1-9H,10H2
InChI key
OUQSGILAXUXMGI-UHFFFAOYSA-N
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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K Suzuki et al.
Chemical & pharmaceutical bulletin, 45(4), 668-674 (1997-04-01)
Two new series of 2-arylmethyl-1,4-benzoquinones (2 and 3) were synthesized for evaluation of their pharmacological activities. These compounds showed significant inhibition of platelet aggregation and some of them possessed a protective against endothelial cell injury. Structure-activity relationship studies indicated that
Heterogeneously Pd/C catalysed procedure for the vinylation of aryl bromides.
Joucla L, et al.
Applied Catalysis A: General, 360(2), 145-153 (2009)
Aromatase and dual aromatase-steroid sulfatase inhibitors from the letrozole and vorozole templates.
Paul M Wood et al.
ChemMedChem, 6(8), 1423-1438 (2011-05-25)
Concurrent inhibition of aromatase and steroid sulfatase (STS) may provide a more effective treatment for hormone-dependent breast cancer than monotherapy against individual enzymes, and several dual aromatase-sulfatase inhibitors (DASIs) have been reported. Three aromatase inhibitors with sub-nanomolar potency, better than
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 513032-50G | 04061832280134 |
| 513032-10G | 04061832280127 |