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About This Item
Linear Formula:
C6H5CH2OC6H4CHO
CAS Number:
Molecular Weight:
212.24
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
98%
form
chunks
mp
56-58 °C (lit.)
SMILES string
O=Cc1cccc(OCc2ccccc2)c1
InChI
1S/C14H12O2/c15-10-13-7-4-8-14(9-13)16-11-12-5-2-1-3-6-12/h1-10H,11H2
InChI key
JAICGBJIBWDEIZ-UHFFFAOYSA-N
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 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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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)
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 Functionalized trans?A2B2?Porphyrins Using Donor?Acceptor Cyclopropane?Derived Dipyrromethanes.
Beyzavi M H, et al.
Advanced Synthesis & Catalysis, 355(7), 1409-1422 (2013)
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)
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