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195405

Sigma-Aldrich

3-(4-Methylphenoxy)benzaldehyde

97%

Synonym(s):

3-(p-Tolyloxy)benzaldehyde

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About This Item

Linear Formula:
CH3C6H4OC6H4CHO
CAS Number:
79124-75-7
Molecular Weight:
212.24
EC Number:
279-068-0
MDL number:
MFCD00003360
UNSPSC Code:
12352100
PubChem Substance ID:
24851690
NACRES:
NA.22

assay

97%

refractive index

n20/D 1.59 (lit.)

bp

140 °C/2 mmHg (lit.)

density

1.102 g/mL at 25 °C (lit.)

functional group

aldehyde

SMILES string

Cc1ccc(Oc2cccc(C=O)c2)cc1

InChI

1S/C14H12O2/c1-11-5-7-13(8-6-11)16-14-4-2-3-12(9-14)10-15/h2-10H,1H3

InChI key

ASKLCRGXIJGVOY-UHFFFAOYSA-N

Application

3-(4-Methylphenoxy)benzaldehyde was used in the synthesis of benzoxazole derivatives of the mannopeptimycin glycopeptide antibiotics.

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
09210DH
21430DO
15828MS
13430KN
11510MR

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Phaik-Eng Sum et al.
Bioorganic & medicinal chemistry letters, 13(15), 2607-2610 (2003-07-11)
A series of benzoxazole derivatives of the mannopeptimycin glycopeptide antibiotics was synthesized via a novel benzoxazole formation reaction by treating aminophenol of mannopeptimycin-beta with an aldehyde and DDQ in DMF. Some of these derivatives (e.g., 5b, 5d, 5m, and 7b)

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