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Merck
CN

47749

Sigma-Aldrich

3-甲酰苯甲酸甲酯

≥98.0% (GC)

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别名:
3-甲醛苯甲酸甲酯
经验公式(希尔记法):
C9H8O3
CAS号:
分子量:
164.16
Beilstein:
2690668
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

≥98.0% (GC)

形式

solid

mp

48-52 °C

SMILES字符串

COC(=O)c1cccc(C=O)c1

InChI

1S/C9H8O3/c1-12-9(11)8-4-2-3-7(5-8)6-10/h2-6H,1H3

InChI key

UVSBCUAQEZINCQ-UHFFFAOYSA-N

应用

Methyl 3-formylbenzoate may be used in the preparation of the following bioactive compounds:
  • meso-Tetrakis(3-carboxyphenyl)porphyrin via condensation with pyrrole.
  • Methyl 3-[4-(1-methyl-3-phenylureido)phenylaminomethyl]benzoate, which shows moderate SENP1 protease inhibition activity.
  • An N-methyl-sulfonylhydrazone derivative for use as anti-diabetic agent with good plasma stability.

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves

法规信息

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Discovery of 1-[4-(N-benzylamino) phenyl]-3-phenylurea derivatives as non-peptidic selective SUMO-sentrin specific protease (SENP) 1 inhibitors.
Uno M, et al.
Bioorganic & Medicinal Chemistry Letters, 22(16), 5169-5173 (2012)
Tetraphilin: a four-helix proton channel built on a tetraphenylporphyrin framework.
Akerfeldt KS, et al.
Journal of the American Chemical Society, 114(24), 9656-9657 (1992)
Synthesis, solubility, plasma stability, and pharmacological evaluation of novel sulfonylhydrazones designed as anti-diabetic agents.
Zapata-Sudo G, et al.
Drug design, development and therapy, 10, 2869-2869 (2016)

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