30000-61-4

Basic information

• Product Name: (PYRROLYL-3)-4 BUTANOIC ACID
• Synonyms: (PYRROLYL-3)-4 BUTANOIC ACID;PYRROLE-3-BUTYRIC ACID;4-(3-PYRROLYL)BUTYRIC ACID;4-(3-Pyrrolyl)butyric acid 95%
• CAS NO: 30000-61-4
• Molecular Formula: C₈H₁₁NO₂
• Molecular Weight: 153.18
• Product Categories: Polypyrroles and Pyrrole MonomersBuilding Blocks;Conducting Polymers and Monomers;Heterocyclic Building Blocks;Organic Conductors and Photovoltaics: OFET and OPV Materials;Pyrroles
• Mol File: 30000-61-4.mol
• Article Data: 3

Chemical Properties

• Melting Point: 91-95 °C
• Boiling Point: 328 °C at 760 mmHg
• Flash Point: 152.2 °C
• Appearance: /
• Density: 1.194 g/cm³
• Vapor Pressure: 7.88E-05mmHg at 25°C
• Refractive Index: 1.553
• Storage Temp.: ?20°C
• CAS DataBase Reference: (PYRROLYL-3)-4 BUTANOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (PYRROLYL-3)-4 BUTANOIC ACID(30000-61-4)
• EPA Substance Registry System: (PYRROLYL-3)-4 BUTANOIC ACID(30000-61-4)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37
• WGK Germany: 3
• Hazardous Substances Data: 30000-61-4(Hazardous Substances Data)

Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 64, p. 3379, 1999 DOI: 10.1021/jo9823339

InChI:InChI=1/C8H11NO2/c10-8(11)3-1-2-7-4-5-9-6-7/h4-6,9H,1-3H2,(H,10,11)

Upstream product

• 86688-99-5 4-<1-(Phenylsulfonyl)-3-pyrrolyl>butyric acid 
• 223393-45-1 methyl 4-<1-(phenylsulfonyl)-3-pyrrolyl>butanoic acid 
• 81454-02-6 4-<1-(Phenylsulfonyl)-3-pyrrolyl>-4-oxobutyric acid 
• 86688-87-1 Methyl 4-<1-(Phenylsulfonyl)-3-pyrrolyl>-4-oxobutyrate 
• 223393-44-0 1-(phenylsulfonyl)-3-pyrrolyl-2-carbomethoxyethyl ketone tosylhydrazone 

Downstream Products

• 134226-34-9 N-(m-vinylphenyl)-1-H-pyrrole-3-butyramide 
• 134226-32-7 N-(p-vinylphenyl)-1-H-pyrrole-3-butyramide 
• 134226-22-5 p-vinylbenzyl 1-H-pyrrole-3-butyrate 
• 300655-18-9 pentafluorophenyl 1H-pyrrole-3-butyrate 

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.

Vinyl Polymers Bearing Pyrrole Ring: I. Syntheses of Pyrroles Having 3-Substituent Bearing Vinyl Group

Pyrroles having 3-substituent bearing the vinyl group with an ester or amide spacer were synthesized starting with 1-(phenylsulfonyl)pyrrole.Homopolymerization of the vinyl monomers thus synthesized provided crosslinked insoluble polymers, but their copolymers with 1-vinyl-2-pyrrolidone were soluble in common solvents.