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Merck
CN

550000

Sigma-Aldrich

3-异丙氧丙胺

≥98%

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别名:
IPOPA
线性分子式:
(CH3)2CHO(CH2)3NH2
CAS号:
分子量:
117.19
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:

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

象形图

FlameCorrosion

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

分析证书(COA)

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Itaconic acid derivatives of sulfanilamide.
Paytash PL, et al.
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.
Bunce RA, et al.
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.
Gein VL, et al.
Pharmaceutical Chemistry Journal, 41(4), 208-210 (2007)
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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