≥97% 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.
2-Thiazolecarboxaldehyde is a thiazole aldehyde derivative. It undergoes Baylis–Hillman reaction with methyl acrylate catalyzed by DABCO (1,4-diazabicyclo[2.2.2]octane).
Thiazole-2-carboxaldehyde may be used as a reactant in the following syntheses Benzothiazine N-acylhydrazones, having potential antinociceptive and anti-inflammatory activity, Thiazole-2-yl-(amino)methylphosphonate diethyl esters, Imino ester by reacting with L-leucine t-butyl ester hydrochloride. Also used in building block for taxane analogs.
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 oxygen compounds |
| Classe | Organooxygen compounds |
| Subclass | Carbonyl compounds |
| Intermediate Tree Nodes | Aldehydes |
| Direct Parent | Aryl-aldehydes |
| Alternative Parents | Thiazoles Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Aryl-aldehyde - Heteroaromatic compound - Thiazole - Azole - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as aryl-aldehydes. These are compounds containing an aldehyde group directly attached to an aromatic ring. |
| External Descriptors | 1,3-thiazole - arenecarbaldehyde |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Article |
|---|---|---|---|
 K2223329 | Certificate of Analysis | Sep 03, 2026 | T107968 |
| A2609027 | Certificate of Analysis | Sep 11, 2024 | T107968 |
| I2424573 | Certificate of Analysis | Sep 11, 2024 | T107968 |
| I2424574 | Certificate of Analysis | Sep 11, 2024 | T107968 |
| I2424575 | Certificate of Analysis | Sep 11, 2024 | T107968 |
| H2003118 | Certificate of Analysis | May 09, 2024 | T107968 |
| H2003116 | Certificate of Analysis | May 09, 2024 | T107968 |
| H1618008 | Certificate of Analysis | Apr 07, 2024 | T107968 |
| D2315355 | Certificate of Analysis | Apr 23, 2023 | T107968 |
| Solubilité | Fully miscible with water. |
|---|---|
| Sensibilité | Air sensitive;Heat sensitive |
| Indice de réfraction | 1.574 |
| Point d'éclair (°C) | 68 °C |
| Point d'ébullition (°C) | 61-63 °C/15 mmHg |
| Poids moléculaire | 113.140 g/mol |
| XLogP3 | 0.700 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 1 |
| Exact Mass | 112.994 Da |
| Monoisotopic Mass | 112.994 Da |
| Topological Polar Surface Area | 58.200 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 76.100 |
| 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 |
