Factory Sells Best Quality 2-Thienyllithium 2786-07-4 with USP
- Molecular Formula: C4H3LiS
- Molecular Weight: 90.0748
- Flash Point: −22 °F
- PSA： 28.24000
- Density: 0.829 g/mL at 25 °C
- LogP: 1.54830
2-Thienyllithium(Cas 2786-07-4) Usage
InChI:InChI=1/C4H3S.Li/c1-2-4-5-3-1;/h1-3H;/rC4H3LiS/c5-4-2-1-3-6-4/h1-3H
2786-07-4 Relevant articles
Cocondensation reactions of heterocyclic aromatic compounds with lithium, calcium and magnesium atoms at 77 K
Mendoza, Oscar,Tacke, Matthias
, p. 1110 - 1116 (2006)
Calcium and magnesium atoms were coconde...
Cocondensation reactions of five-membered heterocycles with lithium atoms at 77 K
Mendoza, Oscar,Rehmann, Franz-Josef K.,Cuffe, Laurence P.,Tacke, Matthias
, p. 4525 - 4532 (2004)
Lithium atoms were cocondensed with eigh...
-
Gilman,Shirley
, p. 1870 (1949)
-
Electrophilic 2-thienylselenenylation of thiophene. Preparation of oligo(seleno-2,5-thienylenes)
Tiecco, Marcello,Testaferri, Lorenzo,Bagnoli, Luana,Marini, Francesca,Temperini, Andrea,Tomassini, Cristina,Santi, Claudio
, p. 3255 - 3260 (2000)
The substitution reactions of thiophene ...
Thiophenylazobenzene: An Alternative Photoisomerization Controlled by Lone-Pair???π Interaction
Slavov, Chavdar,Yang, Chong,Heindl, Andreas H.,Wegner, Hermann A.,Dreuw, Andreas,Wachtveitl, Josef
, p. 380 - 387 (2020)
Azoheteroarene photoswitches have attrac...
Rhodium-Catalyzed Intermolecular Silylation of Csp?H by Silacyclobutanes
He, Tao,Li, Bin,Liu, Lichuan,Ma, Wenpeng,He, Wei
supporting information, p. 5648 - 5652 (2021/03/08)
The signature reactivity of silacyclobut...
LIPIDIC FURAN, PYRROLE, AND THIOPHENE COMPOUNDS FOR USE IN THE TREATMENT OF ATROPHIC VAGINITIS
-
Paragraph 0181; 0182; 0183; 0184; 0185, (2017/11/16)
Provided herein are lipidic furan, pyrro...
Synthesis of Benzosiloles by Intramolecular anti-Hydroarylation via ortho-C-H Activation of Aryloxyethynyl Silanes
Minami, Yasunori,Noguchi, Yuta,Hiyama, Tamejiro
supporting information, p. 14013 - 14016 (2017/10/17)
Straightforward synthesis of benzosilole...
2786-07-4 Process route
-
-
188290-36-0,8014-23-1,25233-34-5
thiophene
-
-
2786-07-4
2-thienyl lithium
| Conditions | Yield |
|---|---|
|
With
tetrahydrofuran; lithium;
at -196.15 ℃;
|
55%
|
|
With
n-butyllithium;
In
tetrahydrofuran;
|
|
|
With
n-butyllithium;
In
tetrahydrofuran;
1. -78 deg C, 15 min, 2. -23 deg C, 30 min;
|
|
|
With
n-butyllithium;
In
tetrahydrofuran; hexane;
at 0 - 20 ℃;
for 1h;
|
|
|
With
n-butyllithium;
In
tetrahydrofuran; hexane;
|
|
|
With
n-butyllithium;
In
tetrahydrofuran; hexane;
at -78 ℃;
|
|
|
With
lithium;
In
tetrahydrofuran;
|
|
|
With
n-butyllithium;
In
tetrahydrofuran; hexane;
at -78 ℃;
for 0.583333h;
|
|
|
With
tert.-butyl lithium;
In
tetrahydrofuran; pentane;
at -78 ℃;
for 2h;
|
|
|
With
n-butyllithium;
In
tetrahydrofuran; hexane;
at 0 ℃;
for 3h;
|
|
|
With
n-butyllithium;
In
tetrahydrofuran;
at -78 ℃;
for 0.5h;
Inert atmosphere;
Schlenk technique;
|
|
|
With
n-butyllithium;
In
tetrahydrofuran; hexane;
at -78 ℃;
for 1h;
|
|
|
With
n-butyllithium;
In
cyclohexane;
at 10 - 20 ℃;
for 2h;
|
|
|
With
n-butyllithium;
In
tetrahydrofuran; hexane;
at 0 ℃;
for 0.5h;
Inert atmosphere;
Schlenk technique;
|
|
|
With
n-butyllithium;
In
tetrahydrofuran; hexane;
|
-
-
188290-36-0,8014-23-1,25233-34-5
thiophene
-
-
109-72-8,29786-93-4
n-butyllithium
-
-
2786-07-4
2-thienyl lithium
| Conditions | Yield |
|---|---|
|
|
|
|
With
diethyl ether;
|
|
|
In
tetrahydrofuran;
at -40 ℃;
for 1h;
|
|
|
In
tetrahydrofuran; hexanes;
for 0.5h;
|
2786-07-4 Upstream products
-
188290-36-0
thiophene
-
109-72-8
n-butyllithium
-
1003-09-4
2-bromothiophene
-
3437-95-4
2-Iodothiophene
2786-07-4 Downstream products
-
34243-33-9
2-thiophen-2-yl-quinoline
-
6165-68-0
thiophene boronic acid
-
100885-90-3
2-methyl-2-phenyl-1-[2]thienyl-propan-1-one
-
101431-05-4
2-ethyl-2-phenyl-1-[2]thienyl-butan-1-one
