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检测方案
≥98%
折射率
n20/D 1.4195 (lit.)
bp
78-79 °C/85 mmHg (lit.)
密度
0.845 g/mL at 25 °C (lit.)
SMILES字符串
CC(C)OCCCN
InChI
1S/C6H15NO/c1-6(2)8-5-3-4-7/h6H,3-5,7H2,1-2H3
InChI key
VHYUNSUGCNKWSO-UHFFFAOYSA-N
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一般描述
3-Isopropoxypropylamine is an aliphatic primary amine.
应用
3-Isopropoxypropylamine may be used as a reactant in the preparation of:
- 1-alcoxyalkyl-5-aryl-4-acyl-3-hydroxy-3-pyrrolin-2-ones
- 1-(p-sulfamyl)-phenyl-5-oxo-3-pyrrolidine carboxylic acid derivative
- ethyl 1,4-dihydro-1-(3-isopropoxypropyl)-4-oxo-3-quinolinecarboxylate
法律信息
Arkema Inc. 产品
警示用语:
Danger
危险声明
危险分类
Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A
WGK
WGK 1
闪点(°F)
closed cup
闪点(°C)
closed cup
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
Itaconic acid derivatives of sulfanilamide.
Journal of the American Chemical Society, 74(18), 4549-4552 (1952)
Ethyl 1, 4-dihydro-4-oxo-3-quinolinecarboxylates by a tandem addition-elimination-SNAr reaction.
Journal of Heterocyclic Chemistry, 48(3), 620-625 (2011)
Synthesis and antibacterial activity of 1-alkoxyalkyl-5-aryl-4-acyl-3-hydroxy-3-pyrrolin-2-ones.
Pharmaceutical Chemistry Journal, 41(4), 208-210 (2007)
Nature communications, 9(1), 4396-4396 (2018-10-26)
New chemical inhibitors of protein-protein interactions are needed to propel advances in molecular pharmacology. Peptoids are peptidomimetic oligomers with the capability to inhibit protein-protein interactions by mimicking protein secondary structure motifs. Here we report the in silico design of a
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