195405
3-(4-Methylphenoxy)benzaldehyde
97%
Synonym(s):
3-(p-Tolyloxy)benzaldehyde
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About This Item
Linear Formula:
CH3C6H4OC6H4CHO
CAS Number:
Molecular Weight:
212.24
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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 Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Synthesis and activity of novel benzoxazole derivatives of mannopeptimycin glycopeptide antibiotics.
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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