500772-25-8

Basic information

• Product Name: 3,5-diphenyldithieno[3,2-b:2',3'-d]thiophene
• Synonyms: 3,5-diphenyldithieno[3,2-b:2',3'-d]thiophene
• CAS NO: 500772-25-8
• Molecular Weight: 348.513
• Mol File: 500772-25-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3,5-diphenyldithieno[3,2-b:2',3'-d]thiophene(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-diphenyldithieno[3,2-b:2',3'-d]thiophene(500772-25-8)
• EPA Substance Registry System: 3,5-diphenyldithieno[3,2-b:2',3'-d]thiophene(500772-25-8)

Safety Data

• Hazardous Substances Data: 500772-25-8(Hazardous Substances Data)

Upstream product

• 502764-54-7 3,5-dibromodithieno[3,2-b:2',3'-d]thiophene 
• 98-80-6 phenylboronic acid 
• 500772-23-6 2,4,5-tribromo-3-phenylthiophene 
• 19698-46-5 2,5-Dibromo-3-phenylthiophene 
• 2404-87-7 3-phenylthiophene 
• 23062-41-1 3-bromo-4-phenylthiophene 
• 500772-24-7 3-phenyl-4-[(4-phenylthien-3-yl)thio]thiophene 

Downstream Products

• 1415917-21-3 C₄₀H₃₆O₄S₃ 
• 911819-24-4 2,6-dibromo-3,5-diphenyldithieno[3,2-b;2',3'-d]thiophene 
• 1487465-00-8 2,6-bis(5-bromothiophen-2-yl)-3,5-diphenyldithieno[3,2-b;2',3'-d]thiophene-S,S-dioxide 
• 1487464-98-1 2,6-dibromo-3,5-diphenyldithieno[3,2-b;2',3'-d]thiophene-S,Sdioxide 
• 500772-30-5 2-(5-methylthien-2-yl)-3,5-diphenyl-6-[5-dimethyl(chloromethyl)silylthien-2-yl]dithieno[3,2-b:2',3'-d]thiophene-4,4-dioxide 
• 500772-29-2 2-bromo-3,5-diphenyl-6-(5-methylthien-2-yl)-dithieno[3,2-b:2',3'-d]thiophene-4,4-dioxide 
• 500772-28-1 2-(5-methylthien-2-yl)-3,5-diphenyl-dithieno[3,2-b:2',3'-d]thiophene-4,4-dioxide 
• 500772-27-0 2-bromo-3,5-diphenyl-dithieno[3,2-b:2',3'-d]thiophene-4,4-dioxide 
• 500772-26-9 3,5-diphenyldithieno[3,2-b:2',3'-d]thiophene-4,4-dioxide 

Relevant articles and documents

A new reaction of P4S10 and Lawesson's reagent; a new method for the synthesis of dithieno[3,2-b;2′,3′-d]thiophenes

A new reaction of P4S10 and Lawesson's reagent for the synthesis of fused thiophenes has been uncovered. It has given easy access to the synthesis of derivatives of the technologically important heterocycle dithieno[3,2-b;2′,3′-d]thiophene, DTT. Electrochemical polymerization of one of the derivatives has been demonstrated.

Selective syntheses of vinylenedithiathiophenes (VDTTs) and dithieno[2,3-b;2′,3′-d]thiophenes (DTTs); Building blocks for π-conjugated systems

Selective syntheses of 3,4-vinylenedithiathiophenes (VDTTs) and dithieno[2,3-b;2′,3′-d]thiophenes (DTTs), having Ph, 4-CH 3OC6H4, 4-BrC6H4, 4-NO2C6H4 and 4-(CH3/