B27005
3-Benzyloxybenzaldehyde
98%
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About This Item
Formule linéaire :
C6H5CH2OC6H4CHO
Numéro CAS:
Poids moléculaire :
212.24
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22
Produits recommandés
Essai
98%
Forme
chunks
Pf
56-58 °C (lit.)
Chaîne SMILES
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
Clé InChI
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.
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
Eyeshields, Gloves, type N95 (US)
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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)
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)
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)
Nasimossadat Banarouei et al.
Mini reviews in medicinal chemistry, 19(8), 679-687 (2018-04-26)
N-aryl derivatives of phthalimide and 4-nitro phthalimide have demonstrated cyclooxygenase inhibitory activity. Also, they possess excellent analgesic and antiinflammatory activity. In this work, a new series of N-arylmethylideneamino derivatives of phthalimide and 4-nitro phthalimide were designed and synthesized. The designed
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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