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513032

Sigma-Aldrich

4-Benzyloxybromobenzene

96%

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About This Item

Linear Formula:
C6H5CH2OC6H4Br
CAS Number:
Molecular Weight:
263.13
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

96%

bp

166-167 °C/4 mmHg (lit.)

mp

60-63 °C (lit.)

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 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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Heterogeneously Pd/C catalysed procedure for the vinylation of aryl bromides.
Joucla L, et al.
Applied Catalysis A: General, 360(2), 145-153 (2009)
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
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
Mingzhang Gao et al.
European journal of medicinal chemistry, 43(10), 2211-2219 (2008-02-15)
The estrogen receptors (ERs) are attractive targets in the treatment of breast cancer and the development of receptor-based breast cancer imaging agents for diagnostic use in biomedical imaging technique positron emission tomography (PET). Tetrahydroisoquinoline derivatives are a class of selective
Synthesis and solid-state self-assembly of polyphenols.
Venkataramanan B, et al.
Crystal Growth & Design, 4(3), 553-561 (2004)

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