Description
Glycine, N-[[2-(3-thienyl)ethoxy]carbonyl]-, butyl ester, homopolymer (CAS: 182691-54-9) is a high-purity synthetic polymer designed for advanced research and industrial applications. This compound, with the molecular formula C13H19NO4S, features a unique thiophene-based structure coupled with a butyl ester group, offering exceptional solubility and reactivity for polymer chemistry studies. Its IUPAC name, butyl 2-(2-thiophen-3-ylethoxycarbonylamino)acetate, reflects its precise chemical configuration. Ideal for material science, pharmaceutical development, and specialty chemical synthesis, this homopolymer is rigorously tested for consistency and performance. Available in various quantities, it is packaged under inert conditions to ensure stability and longevity.
Properties
- CAS Number: 182691-54-9
- Complexity: 286
- IUPAC Name: butyl 2-[2-(3-thienyl)ethoxycarbonylamino]acetate
- InChI: InChI=1S/C13H19NO4S/c1-2-3-6-17-12(15)9-14-13(16)18-7-4-11-5-8-19-10-11/h5,8,10H,2-4,6-7,9H2,1H3,(H,14,16)
- InChI Key: MALISTDSHXWANW-UHFFFAOYSA-N
- Exact Mass: 285.10347926
- Molecular Formula: C13H19NO4S
- Molecular Weight: 285.36
- SMILES: CCCCOC(=O)CNC(=O)OCCC1=CSC=C1
- Topological: 92.9
- Monoisotopic Mass: 285.10347926
- Synonyms: Glycine, N-[[2-(3-thienyl)ethoxy]carbonyl]-, butyl ester, homopolymer, 182691-53-8, 182691-54-9, Butyl((2-(thiophen-3-yl)ethoxy)carbonyl)glycinate, Butyl ((2-(thiophen-3-yl)ethoxy)carbonyl)glycinate
Application
This homopolymer is primarily used in material science for developing conductive polymers due to its thiophene moiety, which enhances electronic properties. It also serves as a building block in pharmaceutical research for drug delivery systems, leveraging its ester functionality for controlled release. Additionally, its solubility in organic solvents makes it suitable for coatings and adhesives in specialty chemical formulations.
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