86688-99-5

Basic information

• Product Name: 4-<1-(Phenylsulfonyl)-3-pyrrolyl>butyric acid
• Synonyms: 4-<1-(Phenylsulfonyl)-3-pyrrolyl>butyric acid
• CAS NO: 86688-99-5
• Molecular Weight: 293.343
• Mol File: 86688-99-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-<1-(Phenylsulfonyl)-3-pyrrolyl>butyric acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-<1-(Phenylsulfonyl)-3-pyrrolyl>butyric acid(86688-99-5)
• EPA Substance Registry System: 4-<1-(Phenylsulfonyl)-3-pyrrolyl>butyric acid(86688-99-5)

Safety Data

• Hazardous Substances Data: 86688-99-5(Hazardous Substances Data)

Upstream product

• 16851-82-4 N-phenylsulfonylpyrrole 
• 81454-02-6 4-<1-(Phenylsulfonyl)-3-pyrrolyl>-4-oxobutyric acid 

Downstream Products

• 1236887-80-1 C₂₃H₁₈N₂O₅S₂ 
• 1236887-81-2 6-[(dimethylamino)methylene]-1-(phenylsulfonyl)-1,4,5,6-tetrahydro-7H-indol-7-one 
• 1236887-58-3 1,7-bis(phenylsulfonyl)-1,4,5,9-tetrahydro-8H-pyrrolo[3,2-h]quinolin-8-one 
• 67839-04-7 1-phenyl-1,4,5,6-tetrahydro-7H-indol-7-one 
• 23456-78-2 1,4,5,6-tetrahydro-7H-indol-7-one 
• 134226-22-5 p-vinylbenzyl 1-H-pyrrole-3-butyrate 
• 134226-32-7 N-(p-vinylphenyl)-1-H-pyrrole-3-butyramide 
• 134226-34-9 N-(m-vinylphenyl)-1-H-pyrrole-3-butyramide 
• 300655-18-9 pentafluorophenyl 1H-pyrrole-3-butyrate 
• 344871-28-9 4-(1-Benzenesulfonyl-1H-pyrrol-3-yl)-butyryl chloride 
• 86689-00-1 1-(phenylsulfonyl)-1,4,5,6-tetrahydro-7H-indol-7-one 
• 30000-61-4 4-(3-pyrrolyl)butanoic acid 

Relevant articles and documents

Strategies towards functionalised electronically conducting organic copolymers: Part 2. Copolymerisation

Here we discuss the application of X-ray photoelectron spectroscopy and absorbance-reflectance FT-IR spectroscopy to establish and quantify reactivity relationships between a range of thiophene and pyrrole monomers. In particular we investigate the application of these techniques to the characterisation of conducting polymer materials grown potentiostatically from solutions containing a binary mixture of monomers. Our data have shown that XPS is especially effective in determining polymer composition and the linear correlation between this and solution composition has enabled prescriptive synthesis of copolymer materials from the different combinations of monomers described here. This technique is much more convenient and more reliable than elemental analysis. In contrast we show that FT-IR studies, whilst providing a useful qualitative guide to the functional group content of the material, do not facilitate detailed quantitative analysis because of large intrinsic errors.