32364-72-0
- Product Name:2,2'-dithiophene-5,5'-dicarboxaldehyde
- Molecular Formula:C10H6 O2 S2
- Purity:99%
- Molecular Weight:222.288
Product Details;
CasNo: 32364-72-0
Molecular Formula: C10H6 O2 S2
factory and supplier 32364-72-0 2,2'-dithiophene-5,5'-dicarboxaldehyde in stock
- Molecular Formula:C10H6 O2 S2
- Molecular Weight:222.288
- Melting Point:213.0 to 217.0 °C
- Boiling Point:426.0±45.0 °C(Predicted)
- PSA:90.62000
- Density:1.415±0.06 g/cm3(Predicted)
- LogP:3.10160
32364-72-0 Relevant articles
Dissymmetrization of Benzothiadiazole by Direct C–H Arylation: A Way to Symmetrical and Unsymmetrical Elongated π-Conjugated Molecules
Dall'Agnese, Chunxiang,Hernández Maldonado, Daniel,Le Borgne, Damien,Moineau-Chane Ching, Kathleen I.
, p. 6872 - 6877 (2017)
5-(7-Bromo-2,1,3-benzothiadiazol-4-yl)-2...
Synthesis of functionalized 2-arylthiophenes with triarylbismuths as atom-efficient multicoupling organometallic nucleophiles under palladium catalysis
Rao, Maddali L. N.,Banerjee, Debasis,Dhanorkar, Ritesh J.
supporting information; experimental part, p. 1324 - 1330 (2011/07/07)
Atom-efficient cross-coupling reactions ...
Palladium-catalysed direct C-H activation/arylation of heteroaromatics: An environmentally attractive access to bi- or polydentate ligands
Derridj, Fazia,Gottumukkala, Aditya L.,Djebbar, Safia,Doucet, Henri
experimental part, p. 2550 - 2559 (2009/03/11)
Bi- or polydentate ligands based on hete...
A convenient catalytic route to symmetrical functionalized bithiophenes
Hassan, Jwanro,Lavenot, Laurence,Gozzi, Christel,Lemaire, Marc
, p. 857 - 858 (2007/10/03)
A series of symmetrical functionalized b...
32364-72-0 Process route
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-
4701-17-1
5-bromo-2-thiophencarboxaldehyde
-
-
5713-61-1
thiophen-2-yl magnesium bromide
-
-
3779-27-9
2,2'-bithiophene-5-carboxaldehyde
-
-
32364-72-0
[2,2']bithiophenyl-5,5'-dicarbaldehyde
-
-
492-97-7
2,2'-Bithiophene
| Conditions | Yield |
|---|---|
|
thiophen-2-yl magnesium bromide;
With
bismuth(III) chloride;
5-bromo-2-thiophencarboxaldehyde;
With
potassium phosphate; palladium diacetate; triphenylphosphine;
In
N,N-dimethyl-formamide;
at 90 ℃;
for 1h;
Inert atmosphere;
|
71% |
-
-
4701-17-1
5-bromo-2-thiophencarboxaldehyde
-
-
4294-57-9
para-methylphenylmagnesium bromide
-
-
32364-72-0
[2,2']bithiophenyl-5,5'-dicarbaldehyde
-
-
38401-68-2
5-(4-methylphenyl)thiophene-2-carbaldehyde
-
-
613-33-2
(4,4'-dimethyl-1,1'-biphenyl)
| Conditions | Yield |
|---|---|
|
para-methylphenylmagnesium bromide;
With
bismuth(III) chloride;
5-bromo-2-thiophencarboxaldehyde;
With
potassium phosphate; palladium diacetate; triphenylphosphine;
In
N,N-dimethyl-formamide;
at 90 ℃;
for 1h;
chemoselective reaction;
Inert atmosphere;
|
60% |
32364-72-0 Upstream products
-
98-03-3
thiophene-2-carbaldehyde
-
71-43-2
benzene
-
4701-17-1
5-bromo-2-thiophencarboxaldehyde
-
554-14-3
2-Methylthiophene
32364-72-0 Downstream products
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596096-87-6
(2,6-dimethyl-phenyl)-{5'-[(2,6-dimethyl-phenyl)-hydroxy-methyl]-[2,2']bithiophenyl-5-yl}-methanol
-
1322125-70-1
bis(4-chloro-N-thiophen-2-ylmethylene-benzenesulfonamide)
-
905457-95-6
(E,E)-5,5'-(bis((2-(4-trifluoromethyl)phenyl)ethenyl))-2,2'-bithiophene
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