31410-07-8
- Product Name：1-Allyl-3-methylimidazolium bromide
- Molecular Formula：C7H11N2Br
- Purity：99%
- Molecular Weight：203.082
Product Details;
CasNo： 31410-07-8
Molecular Formula： C7H11N2Br
factory and manufacture 31410-07-8 1-Allyl-3-methylimidazolium bromide lonic liquid
- Molecular Formula:C7H11N2Br
- Molecular Weight:203.082
- Melting Point:-52.5 °C
- Refractive Index:n20/D 1.578
- PSA：8.81000
- LogP:-2.49740
1-Allyl-3-methylimidazolium bromide(Cas 31410-07-8) Usage
InChI:InChI=1/C7H11N2.BrH/c1-3-4-9-6-5-8(2)7-9;/h3,5-7H,1,4H2,2H3;1H/q+1;/p-1
31410-07-8 Relevant articles
1-Alkenyl-3-methylimidazolium trifluoromethanesulfonate ionic liquids: Novel and low-viscosity ionic liquid electrolytes for dye-sensitized solar cells
Nguyen, Phuong Tuyet,Nguyen, Trang Ngoc,Nguyen, Vinh Son,Nguyen, Hai Truong,Thi Ngo, Dung Kim,Tran, Phuong Hoang
, p. 13142 - 13147 (2018)
Dye-sensitized Solar Cells (DSCs) based ...
Synthesis and thermophysical characterization of novel azide functionalized imidazolium based ionic liquids
Fareghi-Alamdari, Reza,Hatefipour, Razieh
, p. 172 - 178 (2015)
Several new monocationic and unsymmetric...
Allylimidazolium halides as novel room temperature ionic liquids
Mizumo, Tomonobu,Marwanta, Edy,Matsumi, Noriyoshi,Ohno, Hiroyuki
, p. 1360 - 1361 (2004)
Liquid state halide salts composed of im...
Quantum dots in which ionic liquids are ion-bonded and their preparation method
-
Page/Page column 17, (2021/09/01)
A quantum dot particle in which an ionic...
Imidazolium Triflate Ionic Liquid Improves the Activity of ZnCl2 in the Synthesis of Pyrroles and Ketones
Nguyen, Hai Truong,Ngo, Dung Kim Thi,Chau, Khiem Duy Nguyen,Tran, Phuong Hoang
, p. 157 - 165 (2021/03/16)
-
Dimethyldioxirane (DMDO) as a valuable oxidant for the synthesis of polyfunctional aromatic imidazolium monomers bearing epoxides
Chardin,Rouden,Livi,Baudoux
supporting information, p. 5054 - 5059 (2017/11/09)
Conventional organic salts represent a n...
31410-07-8 Process route
-
-
616-47-7
1-methyl-1H-imidazole
-
-
106-95-6
allyl bromide
-
-
31410-07-8
3-allyl-1-methyl-1H-imidazol-3-ium bromide
| Conditions | Yield |
|---|---|
|
With
sodium hydrogencarbonate;
In
acetonitrile;
for 24h;
Inert atmosphere;
|
100% |
|
In
acetonitrile;
at 80 ℃;
|
100% |
|
In
acetonitrile;
at 100 ℃;
for 24h;
Inert atmosphere;
|
99% |
|
In
toluene;
at 20 - 70 ℃;
for 25h;
|
95% |
|
In
toluene;
at 0 - 110 ℃;
for 24h;
|
93% |
|
In
methanol;
at 20 ℃;
for 120h;
|
92% |
|
In
acetonitrile;
at 80 ℃;
for 48h;
|
77.6% |
|
In
benzene;
for 24h;
Ambient temperature;
|
17.5 g |
|
at 65 ℃;
for 12h;
|
|
|
for 2h;
Heating;
|
|
|
at 150 ℃;
for 0.5h;
Microwave irradiation;
Cooling;
neat (no solvent);
|
|
|
at 10 - 20 ℃;
for 12h;
|
|
|
In
neat (no solvent);
at 79.84 ℃;
for 24h;
|
|
|
In
toluene;
at 110 ℃;
|
|
|
In
neat (no solvent);
at 79.84 ℃;
for 24h;
|
|
|
In
acetonitrile;
at 55 ℃;
for 24h;
|
|
|
In
neat (no solvent);
at 100 ℃;
for 0.333333h;
Microwave irradiation;
Sealed tube;
|
|
|
In
dichloromethane;
at 20 ℃;
Cooling with ice;
|
|
|
at 100 ℃;
for 0.5h;
|
-
-
74-83-9
methyl bromide
-
-
31410-01-2
1-allylimidazole
-
-
31410-07-8
3-allyl-1-methyl-1H-imidazol-3-ium bromide
| Conditions | Yield |
|---|---|
|
In
toluene;
at 20 ℃;
|
31410-07-8 Upstream products
-
616-47-7
1-methyl-1H-imidazole
-
106-95-6
allyl bromide
-
74-83-9
methyl bromide
-
31410-01-2
1-allylimidazole
31410-07-8 Downstream products
-
892494-95-0
C7H14BN2O2(1+)*Br(1-)
-
70529-85-0
1-methyl-3-(2-propenyl)-2(3H)-imidazolethione
-
1234553-18-4
3-allyl-1-methylimidazolium octylsulfate
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