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B27005

Sigma-Aldrich

3-Benzyloxybenzaldehyde

98%

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About This Item

Fórmula lineal:
C6H5CH2OC6H4CHO
Número de CAS:
1700-37-4
Peso molecular:
212.24
EC Number:
216-932-8
MDL number:
MFCD00003367
UNSPSC Code:
12352100
PubChem Substance ID:
24891668
NACRES:
NA.22

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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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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)
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)
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)
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
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