All Photos(2)
About This Item
Linear Formula:
C6H5CH2OC6H4Br
CAS Number:
Molecular Weight:
263.13
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
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
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Certificates of Analysis (COA)
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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
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Joucla L, et al.
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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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