Chemistry Heterocyclic Building Blocks Thiophenes Dithieno[3,2-B:2',3'-D]Thiophene

Dithieno[3,2-B:2',3'-D]Thiophene

Halogenation: Dithieno[3,2-b:2',3'-d]thiophene can undergo halogenation reactions where one or more hydrogen atoms are replaced by halogen atoms (e.g., chlorine, bromine). Arylation: Dithieno[3,2-b:2',3'-d]thiophene can undergo arylation reactions where an aryl group is introduced onto the molecule. This can be achieved using various coupling reactions, such as Suzuki-Miyaura coupling, Stille coupling, etc. Alkylation: Alkylation involves the introduction of alkyl groups onto the molecule. This can be done using various alkylating agents under suitable conditions. Oxidation: Dithieno[3,2-b:2',3'-d]thiophene can be oxidized to form its cationic or radical cationic species, which can have unique electronic properties. Reduction: The compound can also undergo reduction reactions to form its anionic or radical anionic species. Cross-Coupling Reactions: Cross-coupling reactions involve the coupling of two different organic molecules to form a new compound. For example, dithieno[3,2-b:2',3'-d]thiophene can be coupled with other aryl or heteroaryl compounds. Cycloaddition Reactions: Dithieno[3,2-b:2',3'-d]thiophene can participate in cycloaddition reactions with suitable dienophiles or other reactive species.

Further Reading:

Framework+−

(9H-Fluoren-9-Yl)Methyl (2-(Thiophen-2-Yl)Ethyl)Carbamate 1-(Thiophen-2-Yl)Ethan-1-One 2,2'-Bithiophene 2,2':5',2''-Terthiophene 2,3-Dihydrothieno[3,4-B][1,4]Dioxine 2,5-Dibromothiophene 2,5-Diphenylthiophene 2-(Thiophen-2-Yl)Pyridine 2-(Trifluoromethyl)Thiophene 2-Chlorothiophene 2-Ethynylthiophene 2-Iodothiophene 2-Methoxythiophene 2-Nitrothiophene 3-Bromothiophene 3-Chlorothiophene 3-Fluorothiophene 3-Methoxythiophene 3-Methylthiophene 3-Nitrothiophene 3-Phenylthiophene 4,4,5,5-Tetramethyl-2-(Thiophen-2-Yl)-1,3,2-Dioxaborolane 4,4,5,5-Tetramethyl-2-(Thiophen-3-Yl)-1,3,2-Dioxaborolane 4,5,6,7-Tetrahydrothieno[2,3-C]Pyridine 4,5,6,7-Tetrahydrothieno[3,2-C]Pyridine 4,7-Di(Thiophen-2-Yl)Benzo[C][1,2,5]Thiadiazole 4,8-Di(Thiophen-2-Yl)Benzo[1,2-B:4,5-B']Dithiophene 4-Phenyl-6H-Thieno[3,2-F][1,2,4]Triazolo[4,3-A][1,4]Diazepine 4H-Cyclopenta[2,1-B:3,4-B']Dithiophene 4H-Thieno[3,2-B]Pyrrole 4H-Thieno[3,4-C]Pyrrole-4,6(5H)-Dione 5,6-Dihydro-4H-Cyclopenta[B]Thiophene 5-(Thiophen-2-Yl)Isoxazole 5-Benzyl-4,5,6,7-Tetrahydrothieno[3,2-C]Pyridine 5-Phenylthiophen-2-Amine Benzo[1,2-B:4,5-B']Dithiophene Dibenzo[B,D]Thiophene Dihydrothiophen-3(2H)-One Dithieno[3,2-B:2',3'-D]Thiophene Ethyl Thiophene-2-Carboxylate Ethyl Thiophene-3-Carboxylate Methyl Thiophene-3-Carboxylate N,N-Diphenyl-4-(Thiophen-2-Yl)Aniline Phenyl(Thiophen-2-Yl)Methanone Thieno[2,3-B]Pyridine Thieno[2,3-C]Pyridine Thieno[2,3-D]Pyrimidine Thieno[3,2-B]Pyridine Thieno[3,2-B]Thiophene Thieno[3,2-C]Pyridine Thieno[3,2-D]Pyrimidine Thieno[3,4-B]Thiophene Thiophen-2-Ylboronic Acid Thiophen-2-Ylmethanol Thiophen-3-Amine Thiophen-3-Ol Thiophene-2-Carbaldehyde Thiophene-2-Carbonitrile Thiophene-3-Carbaldehyde Thiophene-3-Carbonitrile Thiophene-3-Carboxamide Thiophene-3-Carboxylic Acid

By Key Group+−

Acetylthiophene Aminothiophene Bromothieno Chlorothieno Chlorothiophene Cyanothiophene Dibromothieno Dibromothiophene Dichlorothieno Dichlorothiophene Dihydrothieno Dihydrothiophene Dihydroxythiophene Dimethylthieno Dimethylthiophene Dithiophene Fluorothiophene Formylthiophene Hydroxythiophene Iodothieno Iodothiophene Methylthieno Nitrothiophene Oxotetrahydrothiophene Terthiophene Tetrahydrothieno Thiophen-Amine-Hydrochloride Thiophenecarboxaldehyde Thiphen-Amine-Hydrochloride Trithiophene

By Route Intermediates+−

cLogP+−

H-Acceptors+−

H-Donors+−

Polar Surface Area+−

Druglikeness+−

NNCH/NNH+−

sp3-Atoms+−

Non-Aromatic Rings+−

Aromatic Rings+−

Rotatable Bonds+−

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Dithieno[3,2-b:2',3'-d]thiophen-2-ylboronic acid

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A796584183960-95-497%

Dithieno[3,2-b:2',3'-d]thiophen-2-ylboronic acid

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2,6-Dibromodithieno[3,2-b:2',3'-d]thiophene

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A26034667061-69-297% (stabilized with Cu+HQ+MgO)

2,6-Dibromodithieno[3,2-b:2',3'-d]thiophene

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2,6-Bis(trimethylstannyl)dithieno[3,2-b:2',3'-d]thiophene

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A1156336502764-57-099%

2,6-Bis(trimethylstannyl)dithieno[3,2-b:2',3'-d]thiophene

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Diethyl dithieno[3,2-b:2',3'-d]thiophene-2,6-dicarboxylate

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Diethyl dithieno[3,2-b:2',3'-d]thiophene-2,6-dicarboxylate

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Dithieno[3,2-b:2',3'-d]thiophene

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A2478233593-75-798%

Dithieno[3,2-b:2',3'-d]thiophene

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