B27005
3-Benzyloxybenzaldehyde
98%
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About This Item
Linear Formula:
C6H5CH2OC6H4CHO
CAS Number:
Molecular Weight:
212.24
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
216-932-8
MDL number:
Assay:
98%
Form:
chunks
Product Name
3-Benzyloxybenzaldehyde, 98%
InChI key
JAICGBJIBWDEIZ-UHFFFAOYSA-N
InChI
1S/C14H12O2/c15-10-13-7-4-8-14(9-13)16-11-12-5-2-1-3-6-12/h1-10H,11H2
SMILES string
O=Cc1cccc(OCc2ccccc2)c1
assay
98%
form
chunks
mp
56-58 °C (lit.)
Application
Some of the reported applications of 3-benzyloxybenzaldehyde are:
- Synthesis of silybin analogs as anticancer agents that produce apoptosis in ovarian cancer cells through tubulin inhibition.
- Synthesis of porphyrin and boron dipyrromethene (BODIPY) derivatives for fluorescent applications.
- Preparation of styrene copolymers with varying chain mobilities.
- Synthesis of aromatic derivatives of trimethoprim as potential antimalarial agents.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Design and discovery of silybin analogues as antiproliferative compounds using a ring disjunctive?Based, natural product lead optimization approach.
Manivannan E, et al.
European Journal of Medicinal Chemistry, 133, 365-378 (2017)
Novel Copolymers of Styrene. 2. Oxy Ring-Substituted 2-Cyano-3-phenyl 2-propenamides.
Kharas G B, et al.
Journal of Macromolecular Science, Part A: Pure and Applied Chemistry, 50(8), 797-802 (2013)
Synthesis of a novel BODIPY library and its application in the discovery of a fructose sensor.
Zhai D, et al.
ACS Combinatorial Science, 14(2), 81-84 (2012)
Target guided synthesis of 5-benzyl-2, 4-diamonopyrimidines: their antimalarial activities and binding affinities to wild type and mutant dihydrofolate reductases from Plasmodium falciparum.
Sirichaiwat C, et al.
Journal of Medicinal Chemistry, 47(2), 345-354 (2004)
Synthesis of Functionalized trans?A2B2?Porphyrins Using Donor?Acceptor Cyclopropane?Derived Dipyrromethanes.
Beyzavi M H, et al.
Advanced Synthesis & Catalysis, 355(7), 1409-1422 (2013)
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