74707-05-4

Basic information

• Product Name: 2,5-Dibromo-3,4-dimethylthiophene
• Synonyms: 2,5-Dibromo-3,4-dimethylthiophene;NIDAFLYKBAFSNA-UHFFFAOYSA-N
• CAS NO: 74707-05-4
• Molecular Formula: C₆H₆Br₂S
• Molecular Weight: 269.98484
• Mol File: 74707-05-4.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,5-Dibromo-3,4-dimethylthiophene(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Dibromo-3,4-dimethylthiophene(74707-05-4)
• EPA Substance Registry System: 2,5-Dibromo-3,4-dimethylthiophene(74707-05-4)

Safety Data

• Hazardous Substances Data: 74707-05-4(Hazardous Substances Data)

Usage

Chemical compound

2,5-Dibromo-3,4-dimethylthiophene

Structure

Thiophene derivative with two bromine atoms and two methyl groups attached to the carbon atoms in the third and fourth positions

Primary use

Intermediate in the synthesis of other organic compounds, particularly in the production of pharmaceuticals and agrochemicals

Other use

Development of materials for organic electronic devices

Odor

Strong

Potential harm

Potentially harmful if ingested, inhaled, or absorbed through the skin

Safety precautions

Proper safety precautions should be taken when handling this chemical

Upstream product

• 632-15-5 3,4-dimethylthiophene 
• 3141-26-2 3,4-dibromothiophene 
• 75-16-1 methylmagnesium bromide 

Downstream Products

• 55342-12-6 3,4-dimethyl-2,5-diphenylthiophene 
• 74714-03-7 2-Bromo-3,4-dimethyl-5-phenyl-thiophene 
• 77150-78-8 2,5-bis(4-methoxyphenyl)-3,4-dimethylthiophene 
• 56319-03-0 1,4-bis(p-methoxyphenyl)-2,3-dimethylbutane 
• 5701-82-6 1,4-bis(3,4-dimethoxyphenyl)-2,3-dimethylbutane 
• 25347-40-4 2,3-dimethyl-1,4-diphenylbutane 
• 1592480-71-1 C₂₆H₃₂O₄S 

Relevant articles and documents

Electrochromic device having a novel organic compound and

An organic compound having the following general formula [1]: wherein A1 and A2 independently denote a hydrogen atom or a substituent, R7 denotes a hydrogen atom or a substituent, R2 to R5 denote a substituent, R1 and R6 independently denote a hydrogen at

Porphyrin compositions

Novel metal porphyrin compositions useful as organic phosphors are provided. The novel compositions are prepared from commercially available porphyrin-containing starting materials. In one instance a novel palladium-containing porphyrin composition having a number average molecular weight of greater than 12,000 grams per mole was prepared from 5,10,15,20-tetrakis(3′,5′-di(hydroxy)phenyl)-21H-23H-porphyrin by reaction first with palladium(II) acetylacetonate, followed by reaction with 2-bromo-2-methylpropionyl bromide, and subsequent group transfer reaction of the alpha-bromo ester groups with 9,9-dioctyl-2-vinylfluorene in the presence of CuBr as a radical initiator. The product polymer exhibited a number average molecular weight of 12,884 grams per mole, a weight average molecular weight of 14,338 grams per mole, and a robust red phosphorescent emission. Porphyrin containing copoylmers comprising structural units derived from 9,9-dioctyl-2-vinylfluorene and 9-anthracenylmethyl methacrylate were prepared in a similar fashion.