195405
3-(4-甲基苯氧基)苯甲醛
97%
别名:
3-(对甲苯氧基)苯甲醛
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关于此项目
线性分子式:
CH3C6H4OC6H4CHO
化学文摘社编号:
分子量:
212.24
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
279-068-0
MDL number:
Assay:
97%
产品名称
3-(4-甲基苯氧基)苯甲醛, 97%
InChI key
ASKLCRGXIJGVOY-UHFFFAOYSA-N
InChI
1S/C14H12O2/c1-11-5-7-13(8-6-11)16-14-4-2-3-12(9-14)10-15/h2-10H,1H3
SMILES string
Cc1ccc(Oc2cccc(C=O)c2)cc1
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
Application
3-(4-Methylphenoxy)benzaldehyde was used in the synthesis of benzoxazole derivatives of the mannopeptimycin glycopeptide antibiotics.
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
法规信息
新产品
此项目有
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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