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Merck
CN

A9628

2-氨基苯甲醛

≥98%

别名:

2-甲酰苯胺, 邻氨基苯甲醛, 邻胺苄醛

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关于此项目

经验公式(希尔记法):
C7H7NO
化学文摘社编号:
分子量:
121.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
208-454-3
MDL number:
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产品名称

2-氨基苯甲醛, ≥98%

InChI key

FXWFZIRWWNPPOV-UHFFFAOYSA-N

InChI

1S/C7H7NO/c8-7-4-2-1-3-6(7)5-9/h1-5H,8H2

SMILES string

Nc1ccccc1C=O

assay

≥98%

form

powder

shipped in

dry ice

storage temp.

−20°C

Quality Level

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Application

以下反应的反应物:
  • 制备作为抗病毒剂的喹啉衍生物
  • 制备用于OLED的电致发光材料
  • Friedlander型合成
  • 制备用于金催化的环丙基甲醇重排的2-甲苯氨基苯基环丙基甲醇
  • 羟基-TEMPO催化的芳基甲胺的苄基C-H键胺化
  • 银催化的苯胺介导的级联加氢胺化/环加成反应

Disclaimer

可在室温下快速聚合。如果存在少量聚合物,可在乙醇中生成略微浑浊的溶液。

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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H R Kim et al.
Analytical biochemistry, 223(2), 205-207 (1994-12-01)
We developed an assay system for ornithine aminotransferase (EC 2.6.1.13) using ninhydrin. Pyrroline 5-carboxylate, a product of enzymatic transamination, reacts with ninhydrin under hot acidic conditions to form a reddish pigment soluble in ethanol. The millimolar extinction coefficient of reaction
Yi-Feng Wang et al.
Chemistry, an Asian journal, 4(12), 1834-1838 (2009-10-16)
Generally, amine-catalyzed enantioselective transformations rely on chiral enamine or unsaturated iminium intermediates. Herein, we report a protocol involving dual activation by an aromatic iminium and hydrogen-bonding. An enantioselective aza-Michael-Henry domino reaction of 2-aminobenzaldehydes with nitroolefins has been developed through this
Shoko Yamazaki et al.
The Journal of organic chemistry, 75(4), 1188-1196 (2010-01-30)
Quinolines are an important class of compounds, and the development of new efficient synthetic strategies for the construction of quinolines is of considerable interest. Zinc triflate catalyzed cyclization of ethenetricarboxylate derivatives with 2-aminobenzaldehydes has been examined. The reaction of ethenetricarboxylate
Moamen S Refat et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 70(1), 234-242 (2007-09-04)
The, nitrin, 2-aminobenzaldehyde phenylhydrazone (2ABPH) was synthesis by refluxing 2-nitrobenzaldehyde with phenylhydrazine in ethanolic solvent. Three transition metal (II) complexes of 2ABPH have been prepared. Elemental analysis, molar conductivity, IR, UV, 1H NMR, and mass spectra, as well as TG/DTG
Sarah C Atkinson et al.
Structure (London, England : 1993), 26(7), 948-959 (2018-05-29)
Protein dynamics manifested through structural flexibility play a central role in the function of biological molecules. Here we explore the substrate-mediated change in protein flexibility of an antibiotic target enzyme, Clostridium botulinum dihydrodipicolinate synthase. We demonstrate that the substrate, pyruvate

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