550000
3-Isopropoxypropylamine
≥98%
Synonym(s):
IPOPA
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About This Item
Linear Formula:
(CH3)2CHO(CH2)3NH2
CAS Number:
Molecular Weight:
117.19
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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
SMILES string
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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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
Product of Arkema Inc.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point(F)
102.2 °F - closed cup
Flash Point(C)
39 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
危险化学品
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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)
Itaconic acid derivatives of sulfanilamide.
Paytash PL, et al.
Journal of the American Chemical Society, 74(18), 4549-4552 (1952)
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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