83275
4-吡咯烷基吡啶
purum, ≥98.0% (NT)
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关于此项目
经验公式（希尔记法）:
C9H12N2
化学文摘社编号:
分子量:
148.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
219-534-2
Beilstein/REAXYS Number:
472443
MDL number:
Assay:
≥98.0% (NT)
Form:
crystals
grade
purum
Quality Level
assay
≥98.0% (NT)
form
crystals
mp
54-58 °C (lit.), 55-61 °C
solubility
methanol: 0.1 g/mL, clear
SMILES string
C1CCN(C1)c2ccncc2
InChI
1S/C9H12N2/c1-2-8-11(7-1)9-3-5-10-6-4-9/h3-6H,1-2,7-8H2
InChI key
RGUKYNXWOWSRET-UHFFFAOYSA-N
Other Notes
超强亲核酰化反应催化剂。综述
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Skin Corr. 1B
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
233.6 °F - closed cup
flash_point_c
112 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
A. Hassner
Tetrahedron, 34, 2069-2069 (1978)
Brian L Hodous et al.
Journal of the American Chemical Society, 124(34), 10006-10007 (2002-08-22)
The first method for the catalytic enantioselective addition of amines (specifically, pyrroles) to ketenes has been developed, and it has been demonstrated that the resulting acylpyrroles can be transformed into a broad spectrum of useful derivatives. On the basis of
Hoefle, G., et al.
Angewandte Chemie (International Edition in English), 90, 602-602 (1978)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 83275-5G | 04061832541358 |
| 83275-25G | 04061832541341 |