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Sigma-Aldrich

4-Phenoxybenzaldehyde

98%

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5 G
MXP 1,861.00

MXP 1,861.00

Estimated to ship onApril 17, 2025

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5 G
MXP 1,861.00

About This Item

Linear Formula:
C6H5OC6H4CHO
CAS Number:
67-36-7
Molecular Weight:
198.22
Beilstein:
1947841
EC Number:
200-650-7
MDL number:
MFCD00003383
UNSPSC Code:
12352100
PubChem Substance ID:
24852664
NACRES:
NA.22

MXP 1,861.00

Estimated to ship onApril 17, 2025

Request a Bulk Order

Quality Level

100

Assay

98%

refractive index

n20/D 1.611 (lit.)

bp

185 °C/14 mmHg (lit.)

mp

24-25 °C (lit.)

density

1.132 g/mL at 25 °C (lit.)

functional group

aldehyde
phenoxy

SMILES string

O=Cc1ccc(Oc2ccccc2)cc1

InChI

1S/C13H10O2/c14-10-11-6-8-13(9-7-11)15-12-4-2-1-3-5-12/h1-10H

InChI key

QWLHJVDRPZNVBS-UHFFFAOYSA-N

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Application

4-Phenoxybenzaldehyde was used in the synthesis of:
  • spirodiketopiperazine derivatives[1]
  • benzoxazoles[2]

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000381071
0000381071
0000273824
0000204320
0000273824

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Kelly J McClure et al.
Bioorganic & medicinal chemistry letters, 16(7), 1924-1928 (2006-01-31)
In a recent paper, [Arienti, K. L.; Brunmark, A.; Axe, F. U.; McClure, K. M.; Lee, A.; Blevitt, J.; Neff, D. K.; Huang, L.; Crawford, S.; Chennagiri, R. P.; Karlsson, L.; Brietenbucher, J. G. J. Med. Chem.2005, 48, 1873], we
Rena Nishizawa et al.
Bioorganic & medicinal chemistry letters, 17(3), 727-731 (2006-11-23)
Hydroxylated derivatives were designed and synthesized based on the information of oxidative metabolites. Compounds derived from beta-substituted (2R,3R)-2-amino-3-hydroxypropionic acid showed improved inhibitory activities against the binding of MIP-1alpha to human CCR5, compared with the non-hydroxylated derivatives and the other isomers.
Vikas N Telvekar et al.
Bioorganic & medicinal chemistry letters, 22(1), 649-652 (2011-11-15)
A series of structurally novel, substituted 2-(2-(4-aryloxybenzylidene) hydrazinyl)benzothiazole derivatives incorporating 2-hydrazinyl benzothiazole and 4-(aryloxy)benzaldehyde were designed and synthesized using molecular hybridization approach. All the synthesized compounds exhibited promising activity (MIC 1.5-29.00μg/ml) against Mycobacteriumtuberculosis H37Rv strains of using REMA. Five of

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