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Chinese Factory Supply Wholesale 2-Chloromethyl-1,3-dioxolane 2568-30-1 with Cheap Price
- Molecular Formula: C4H7ClO2
- Molecular Weight: 122.551
- Appearance/Colour: Colourless liquid
- Vapor Pressure: 3.97mmHg at 25°C
- Refractive Index: n20/D 1.449(lit.)
- Boiling Point: 155.072 °C at 760 mmHg
- Flash Point: 60 °C
- PSA: 18.46000
- Density: 1.187 g/cm3
- LogP: 0.59810
2-Chloromethyl-1,3-dioxolane(Cas 2568-30-1) Usage
|
General Description |
2-Chloromethyl-1,3-dioxolane is commonly used in industrial manufacturing processes. |
InChI:InChI=1/C4H7ClO2/c5-3-4-6-1-2-7-4/h4H,1-3H2
2568-30-1 Relevant articles
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Astle,Pierce
, p. 178,179 (1955)
-
Polyesters by a Radical Pathway: Rationalization of the Cyclic Ketene Acetal Efficiency
Gigmes, Didier,Gil, Noémie,Guillaneuf, Yohann,Lefay, Catherine,Plummer, Christopher M.,Siri, Didier,Tardy, Antoine
supporting information, p. 14517 - 14526 (2020/07/13)
Radical ring-opening polymerization (rRO...
PROCESS FOR PREPARING CHLOROACETALDEHYDE ACETALS
-
Paragraph 0034; 0035, (2016/10/11)
The invention relates to a process for p...
Phosphorus promoted SO42-/TiO2 solid acid catalyst for acetalization reaction
Zhong, Shaofeng,Ou, Qiongrong,Shao, Linjun
, p. 3005 - 3008 (2015/11/27)
A novel phosphorus modifed SO42-/TiO2 ca...
Preparation of a novel solid acid catalyst with Lewis and Bronsted acid sites and its application in acetalization
Du, Yijun,Shao, Linjun,Luo, Lingyan,Shi, Si,Qi, Chenze
, p. 157 - 163 (2014/02/14)
A novel melamine-formaldehyde resin (MFR...
2568-30-1 Process route
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107-20-0
2-chloroethanal
-
-
107-21-1
ethylene glycol
-
-
2568-30-1
2-chloromethyl-1,3-dioxolane
| Conditions | Yield |
|---|---|
|
With
sulfonic group functionalized polyacrylonitrile preoxidated nanofiber mat;
In
cyclohexane;
at 150 ℃;
for 2h;
Dean-Stark;
|
99.6%
|
|
With
phosphorus modified SO4(2-)/TiO2;
In
cyclohexane;
for 2h;
Dean-Stark;
Reflux;
|
99%
|
|
With
polyacrylonitrile hybrid fiber mat supported solid acid catalyst;
In
cyclohexane;
Reflux;
|
97.85%
|
|
With
toluene-4-sulfonic acid;
In
chloroform;
for 7h;
Reflux;
|
91%
|
|
With
cyclohexane;
for 2h;
Dean-Stark;
|
90%
|
|
With
cation exchanger; benzene;
Unter Entfernen des entstehenden Wassers;
|
|
|
at 80 ℃;
for 2h;
Yield given;
|
|
|
With
[SOClMIm]Cl;
at 16 ℃;
for 23h;
|
|
|
With
C13H16NO3S(1+)*0.5Cu(2+)*O4S(2-);
In
cyclohexane;
for 0.5h;
Reflux;
|
99 %Chromat.
|
|
With
solid acidic polymeric ionic liquid from [SO3H(CH2)3VIm]HSO4 and resorcinol-formaldehyde resin;
In
cyclohexane;
for 0.5h;
Reflux;
Dean-Stark;
|
99 %Chromat.
|
|
With
melamine formaldehyde resin supported ionic liquid and cuprous catalyst;
In
cyclohexane;
for 2h;
Dean-Stark;
Reflux;
|
88.3 %Chromat.
|
-
-
97-97-2
chloroacetaldehyde dimethyl acetal
-
-
107-21-1
ethylene glycol
-
-
2568-30-1
2-chloromethyl-1,3-dioxolane
| Conditions | Yield |
|---|---|
|
|
94%
|
|
With
Dowex 50(H+);
at 120 ℃;
for 1h;
|
93%
|
|
With
sulfuric acid;
|
|
|
With
hydrogenchloride;
|
|
|
sulfuric acid;
|
|
|
With
toluene-4-sulfonic acid;
at 115 ℃;
for 5h;
|
2568-30-1 Upstream products
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4362-41-8
2-(chloromethylene)-1,3-dioxolane
-
107-20-0
2-chloroethanal
-
107-21-1
ethylene glycol
-
97-97-2
chloroacetaldehyde dimethyl acetal
2568-30-1 Downstream products
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96-50-4
2-thiazolylamine
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5694-68-8
2-hydroxymethyl-1,3-dioxolane
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179669-44-4
dioxolanne de l'α-phenylthioacetaldehyde
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57366-77-5
1-(1,3-dioxolan-2-yl)-N-methylmethanamine