557811
2,4-Diisopropylphenol
98%
Synonym(s):
2,4-Bis(1-methylethyl)phenol, 2,4-Bis(propan-2-yl)phenol, 2,4-Di(propan-2-yl)phenol
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About This Item
Linear Formula:
[(CH3)2CH]2C6H3OH
CAS Number:
Molecular Weight:
178.27
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
220-906-1
MDL number:
Assay:
98%
Quality Level
assay
98%
refractive index
n20/D 1.5130 (lit.)
bp
79-80 °C (lit.)
density
0.948 g/mL at 25 °C (lit.)
SMILES string
CC(C)c1ccc(O)c(c1)C(C)C
InChI
1S/C12H18O/c1-8(2)10-5-6-12(13)11(7-10)9(3)4/h5-9,13H,1-4H3
InChI key
KEUMBYCOWGLRBQ-UHFFFAOYSA-N
General description
2,4-Diisopropylphenol, commonly known as 2,4-propofol, is an isomeric form of propofol. EC50 Microtox (5min, 25°C) assay value of 2,4-diisopropylphenol is 2x10-4mM. It is formed as one of the reaction products from the reaction between boron fluoride with isopropyl phenyl ether.
Application
2,4-Diisopropylphenol may be used in the preparation of N,N-bis(3,5-diisopropyl-2-hydroxybenyl)-N′,N′-dimethyl-1,2-diaminoethane.
hcodes
signalword
Warning
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Organic Reactions with Boron Fluoride. V. The Rearrangement of Isopropylphenol, o-, m-and p-Cresyl Ethers.
Sowa FJ, et al.
Journal of the American Chemical Society, 55(8), 3402-3407 (1933)
rac-Lactide polymerization using aluminum complexes bearing tetradentate phenoxy-amine ligands.
Tang Z and Gibson VC.
European Polymer Journal, 43(1), 150-155 (2007)
Shanker Karunanithi et al.
eNeuro, 7(1) (2020-02-06)
Propofol is the most common general anesthetic used for surgery in humans, yet its complete mechanism of action remains elusive. In addition to potentiating inhibitory synapses in the brain, propofol also impairs excitatory neurotransmission. We use electrophysiological recordings from individual