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B27005

3-Benzyloxybenzaldehyde

Name: 3-Benzyloxybenzaldehyde
Brand: ALDRICH

98%

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About This Item

Linear Formula:

C₆H₅CH₂OC₆H₄CHO

CAS Number:

1700-37-4

Molecular Weight:

212.24

NACRES:

NA.22

PubChem Substance ID:

24891668

UNSPSC Code:

12352100

EC Number:

216-932-8

MDL number:

MFCD00003367

Assay:

98%

Form:

chunks

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Properties

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

Description

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)

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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Global Trade Item Number

SKU	GTIN
B27005-100G	04061831823639
B27005-25G	04061831832556
B27005-5G	04061831811872