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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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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
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
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.
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
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

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