Determine the necessary mass, volume, or concentration for preparing a solution.
Mw 100000 for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Poly (vinyl cinnamate) is a cross-linkable conjugated polymer with a reactive functional group in the main chain. Its backbone contains polyvinyl alcohol and cinnamoyl groups
Application:
Poly (vinyl cinnamate) has been used to study the cyclodimerization of poly (vinyl cinnamate) in solution using pyrylium and thiopyrylium salts. It can also be used to synthesize photocurable polymer gate dielectricsto fabricate cylindrical organic field-effect transistors
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Phenylpropanoids and polyketides |
| Classe | Cinnamic acids and derivatives |
| Subclass | Cinnamic acids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Cinnamic acids |
| Alternative Parents | Styrenes Monocarboxylic acids and derivatives Enols Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Not available |
| Substituents | Cinnamic acid - Styrene - Benzenoid - Monocyclic benzene moiety - Monocarboxylic acid or derivatives - Enol - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aromatic homomonocyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as cinnamic acids. These are organic aromatic compounds containing a benzene and a carboxylic acid group forming 3-phenylprop-2-enoic acid. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
| Certificate of Analysis | Jul 28, 2023 | P478163 | |
| Certificate of Analysis | Jul 28, 2023 | P478163 | |
| Certificate of Analysis | Jul 28, 2023 | P478163 | |
| Certificate of Analysis | Jul 28, 2023 | P478163 | |
| Certificate of Analysis | Jul 28, 2023 | P478163 | |
| Certificate of Analysis | Jul 28, 2023 | P478163 |
| Peso molecolare | 192.210 g/mol |
|---|---|
| XLogP3 | |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 2 |
| Exact Mass | 192.079 Da |
| Monoisotopic Mass | 192.079 Da |
| Topological Polar Surface Area | 57.500 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 165.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 1 |
| Covalently-Bonded Unit Count | 2 |