登录 查看组织和合同定价。
选择尺寸
变更视图
关于此项目
经验公式(希尔记法):
C8H4KNO2
化学文摘社编号:
分子量:
185.22
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
214-046-6
Beilstein/REAXYS Number:
3598719
MDL number:
Assay:
≥99.0% (NT)
Form:
powder
grade
purum
Quality Level
assay
≥99.0% (NT)
form
powder
impurities
≤0.5% water
mp
>300 °C (lit.)
functional group
imide
SMILES string
[K]N1C(=O)c2ccccc2C1=O
InChI
1S/C8H5NO2.K/c10-7-5-3-1-2-4-6(5)8(11)9-7;/h1-4H,(H,9,10,11);/q;+1/p-1
InChI key
FYRHIOVKTDQVFC-UHFFFAOYSA-M
Application
Phthalimide potassium salt (PPI) is widely used for the synthesis of primary amines from corresponding alkyl halides, known as Gabriel synthesis. Some of the other applications are:
- Preparation of phthalimidogold precatalyst for gold catalysis.
- It can be used in the palladium-catalyzed enantioselective synthesis of α- and β-amino acids.
- Potassium phthalimide is as an effective organocatalyst for the cyanosilylation of carbonyl compounds to synthesize cyanohydrin trimethylsilyl ethers.
Still not finding the right product?
Explore all of our products under 酞酰亚胺 钾盐
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
346.3 °F - closed cup
flash_point_c
174.6 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
One-pot synthesis of core-expanded naphthalene diimides: enabling N-substituent modulation for diverse n-type organic materials.
Hu Y, et al.
Organic Letters, 14(1), 292-295 (2011)
Palladium-catalysed asymmetric allylic substitution: synthesis of α-and β-amino acids.
Bower J F, et al.
Journal of the Chemical Society. Perkin Transactions 1, 9, 1411-1420 (1997)
A facile one-pot synthesis of N-substituted phthalimides using a catalytic amount of crown ether.
Soai K, et al.
Bulletin of the Chemical Society of Japan, 55(5), 1671-1672 (1982)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 79790-500G | 04061831832419 |
| 79790-100G | 04061831823448 |
