550000
3-异丙氧丙胺
≥98%
别名:
IPOPA
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关于此项目
线性分子式:
(CH3)2CHO(CH2)3NH2
化学文摘社编号:
分子量:
117.19
UNSPSC Code:
12352100
PubChem Substance ID:
EC Number:
220-816-2
MDL number:
Assay:
≥98%
InChI key
VHYUNSUGCNKWSO-UHFFFAOYSA-N
InChI
1S/C6H15NO/c1-6(2)8-5-3-4-7/h6H,3-5,7H2,1-2H3
SMILES string
CC(C)OCCCN
assay
≥98%
refractive index
n20/D 1.4195 (lit.)
bp
78-79 °C/85 mmHg (lit.)
density
0.845 g/mL at 25 °C (lit.)
functional group
amine, ether
General description
3-Isopropoxypropylamine is an aliphatic primary amine.
Application
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
Legal Information
Arkema Inc. 产品
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A
存储类别
3 - Flammable liquids
wgk
WGK 1
flash_point_f
102.2 °F - closed cup
flash_point_c
39 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Itaconic acid derivatives of sulfanilamide.
Paytash PL, et al.
Journal of the American Chemical Society, 74(18), 4549-4552 (1952)
Synthesis and antibacterial activity of 1-alkoxyalkyl-5-aryl-4-acyl-3-hydroxy-3-pyrrolin-2-ones.
Gein VL, et al.
Pharmaceutical Chemistry Journal, 41(4), 208-210 (2007)
Ethyl 1, 4-dihydro-4-oxo-3-quinolinecarboxylates by a tandem addition-elimination-SNAr reaction.
Bunce RA, et al.
Journal of Heterocyclic Chemistry, 48(3), 620-625 (2011)
Jeffrey A Schneider et al.
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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