Determine the necessary mass, volume, or concentration for preparing a solution.
≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Argon charged Ships Wet ice 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.
Propargyl chloroformate is a propargyl ester. It serves as a protecting group for the hydroxy and amino functional group. Rates of solvolysis of propargyl chloroformate has been analyzed in various solvents of widely varying nucleophilicity and ionizing power values using the extended Grunwald-Winstein equation.Propargyl chloroformate may be used for the preparation of the following:binaphthol-diacetylene derivativespropargyl pentafluorophenyl carbonateN-Poc protected amino acids (Poc = propargyloxycarbonyl)
| Pubchem Sid | 488194369 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488194369 |
| Sorrisi canonici | C#CCOC(=O)Cl |
| IUPAC Name | prop-2-ynyl carbonochloridate |
| InChIKey | RAMTXCRMKBFPRG-UHFFFAOYSA-N |
| INCHI | 1S/C4H3ClO2/c1-2-3-7-4(5)6/h1H,3H2 |
| Isomeri SMILES | C#CCOC(=O)Cl |
| WGK Germania | 3 |
| PubChem CID | 3356829 |
| Peso molecolare | 118.52 |
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 | Organic acids and derivatives |
| Classe | Organic carbonic acids and derivatives |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Organic carbonic acids and derivatives |
| Alternative Parents | Acetylides Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Carbonic acid derivative - Acetylide - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organochloride - Organohalogen compound - Carbonyl group - Aliphatic acyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as organic carbonic acids and derivatives. These are compounds comprising the organic carbonic acid or a derivative thereof. |
| 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 | Mar 13, 2026 | P468141 | |
| Certificate of Analysis | Mar 13, 2026 | P468141 | |
| Certificate of Analysis | Jan 19, 2026 | P468141 | |
| Certificate of Analysis | Jan 19, 2026 | P468141 | |
| Certificate of Analysis | Jun 28, 2024 | P468141 | |
| Certificate of Analysis | Jun 28, 2024 | P468141 | |
| Certificate of Analysis | Mar 06, 2023 | P468141 | |
| Certificate of Analysis | Mar 06, 2023 | P468141 |
| Punto di infiammabilità (°F) | 86 °F |
|---|---|
| Punto di infiammabilità (°C) | 30 °C |
| Peso molecolare | 118.520 g/mol |
| XLogP3 | 1.300 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 117.982 Da |
| Monoisotopic Mass | 117.982 Da |
| Topological Polar Surface Area | 26.300 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 110.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |