2-isopropoxy-2-methylpropane
- Name 2-isopropoxy-2-methylpropane
- CAS 17348-59-3
- Purity 99%
Product Details
Factory Export Top Purity 2-isopropoxy-2-methylpropane 17348-59-3 In Stock
- Molecular Formula: C7H16O
- Molecular Weight: 116.203
- Vapor Pressure: 71.2mmHg at 25°C
- Melting Point: -95.35°C
- Refractive Index: 1.394
- Boiling Point: 87.6°C at 760mmHg
- PSA： 9.23000
- Density: 0.77g/cm3
- LogP: 2.20990
2-isopropoxy-2-methylpropane(Cas 17348-59-3) Usage
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General Description |
2-Isopropoxy-2-methylpropane, also known as tert-butyl isopropyl ether, is a chemical compound with the molecular formula C7H16O. It is a colorless, flammable liquid that is commonly used as a solvent in various industrial and laboratory applications. It is also used as a fuel additive, in the production of pharmaceuticals, and as a component in the manufacturing of fragrances and flavors. The chemical is known for its low toxicity and low environmental impact, making it a relatively safe and versatile compound for use in a wide range of industries. |
InChI:InChI=1/C7H16O/c1-6(2)8-7(3,4)5/h6H,1-5H3
17348-59-3 Relevant articles
Kinetics and mechanism of N-Boc cleavage: Evidence of a second-order dependence upon acid concentration
Ashworth, Ian W.,Cox, Brian G.,Meyrick, Brian
, p. 8117 - 8125 (2010)
The kinetics of the HCl-catalyzed deprot...
METHOD FOR PRODUCING ASYMMETRIC ALKYL ETHER HAVING TERTIARY ALKYL GROUP
-
Paragraph 0021, (2017/01/31)
PROBLEM TO BE SOLVED: To provide a metho...
Kinetics of the reactions of tert-butanol with C2-C5 alcohols on sulfo cation exchangers
Golovanov,Pisareva,Levshenkov
, p. 179 - 183 (2013/05/22)
The kinetics of etherification of tert-b...
Specifics of the synthesis of some alkyl tert-alkyl ethers and their thermodynamic properties
Krasnykh,Levanova,Karaseva,Kirgizova,Varushchenko,Druzhinina,Pashchenko
, p. 92 - 95 (2007/10/03)
The conditions of synthesis and isolatio...
17348-59-3 Process route
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![isopropyl N-{5-({[(2S,4S)-1-(tert-butoxycarbonyl)-4-(pyridin-3-ylcarbonyl)thiopyrrolidin-2-yl]methyl}amino)-2-[2-(4-fluorophenyl)ethyl]benzoyl}-L-methioninate](/upload/2026/5/5021ee44bbe641e69069ab175cd99470_85b46975-e763-4309-91af-c40930f28e0c.png)
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345915-09-5
isopropyl N-{5-({[(2S,4S)-1-(tert-butoxycarbonyl)-4-(pyridin-3-ylcarbonyl)thiopyrrolidin-2-yl]methyl}amino)-2-[2-(4-fluorophenyl)ethyl]benzoyl}-L-methioninate
-
-
67-63-0,8013-70-5
isopropyl alcohol
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![isopropyl N-{5-({[(2S,4S)-4-(pyridin-3-ylcarbonyl)thiopyrrolidin-2-yl]methyl}amino)-2-[2-(4-fluorophenyl)ethyl]benzoyl}-L-methioninate](/upload/2026/5/5a759c94f4db4c7fa7be83b8fec107fb_7b05496d-571b-4964-afc2-be4951784900.png)
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345915-10-8
isopropyl N-{5-({[(2S,4S)-4-(pyridin-3-ylcarbonyl)thiopyrrolidin-2-yl]methyl}amino)-2-[2-(4-fluorophenyl)ethyl]benzoyl}-L-methioninate
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-
507-20-0
tertiary butyl chloride
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-
17348-59-3
isopropyl tert-butyl ether
| Conditions | Yield |
|---|---|
|
With
hydrogenchloride;
In
toluene;
at 50 ℃;
Concentration;
Temperature;
Kinetics;
Inert atmosphere;
|
-
-
4-Chloro-phenol; compound with 2-isopropoxy-2-methyl-propane
-
-
17348-59-3
isopropyl tert-butyl ether
-
-
106-48-9,82344-39-6
4-chloro-phenol
| Conditions | Yield |
|---|---|
|
In
cyclohexane;
at 20 ℃;
Equilibrium constant;
|
17348-59-3 Upstream products
-
507-20-0
tertiary butyl chloride
-
67-63-0
isopropyl alcohol
-
115-11-7
isobutene
-
75-65-0
tert -butyl alcohol
17348-59-3 Downstream products
-
67-63-0
isopropyl alcohol
-
115-11-7
isobutene
-
67-64-1
acetone
-
75-65-0
tert -butyl alcohol
