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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:
529-23-7
分子量:
121.14
NACRES:
NA.22
PubChem Substance ID:
57653901
UNSPSC Code:
12352100
EC Number:
208-454-3
MDL number:
MFCD00007709
Assay:
≥98%
Form:
powder
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Quality Level

200

assay

≥98%

form

powder

shipped in

dry ice

storage temp.

−20°C

SMILES string

Nc1ccccc1C=O

InChI

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

InChI key

FXWFZIRWWNPPOV-UHFFFAOYSA-N

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
GHS07

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
0000482791
0000482790
0000482791
0000482790
HMBK7122

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Riccardo Montioli et al.
The FEBS journal, 286(14), 2787-2798 (2019-04-09)
Among the over 50 gyrate atrophy-causing mutations of ornithine δ-aminotransferase (OAT), the R180T involves an active site residue located at the dimer interface, which in the crystal structure of OAT complexed with 5-fluoromethylornithine engages a salt bridge with the α-carboxylate
Riccardo Montioli et al.
Biochimica et biophysica acta. Molecular basis of disease, 1864(11), 3629-3638 (2018-09-27)
Gyrate atrophy (GA) is a rare recessive disorder characterized by progressive blindness, chorioretinal degeneration and systemic hyperornithinemia. GA is caused by point mutations in the gene encoding ornithine δ-aminotransferase (OAT), a tetrameric pyridoxal 5'-phosphate-dependent enzyme catalysing the transamination of l-ornithine
Michael C Haibach et al.
Journal of the American Chemical Society, 133(7), 2100-2103 (2011-02-02)
Aminobenzaldehydes react with indoles in an unprecedented cascade reaction. This acid-catalyzed redox-neutral annulation proceeds via a condensation/1,5-hydride shift/ring-closure sequence. Polycyclic azepinoindoles and related compounds are obtained in a single step with good to excellent yields.
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全球贸易项目编号

货号GTIN
A9628-500MG04061833408124
A9628-100MG04061831823608
A9628-1G04061833403686