I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.
Stock No. | Size | Price ($) | Quantity | Availability |
---|---|---|---|---|
L01329-22 | 100g | 125.00 |
|
|
Acetaldehyde anion synthon, by metallation at the methyl group. ɑ-Mono-, di- and trisubstituted aldehydes can be prepared by successive lithiation and alkylation steps. The anion also reacts, e.g.with carbonyl groups to give precursors of ß-hydroxy aldehydes. The thiazoline residue can be removed by reduction with Al amalgam and treatment with HgCl2: J. Org. Chem., 40, 2021, 2025 (1975). Compare Thiazole, L09970, 2-Bromothiazole, A14838, and 2-(Trimethylsilyl)thiazole, B21903.
/nHazard Statements: H226
Flammable liquid and vapour.
Precautionary Statements: P210-P233-P240-P241-P242-P243-P280-P303+P361+P353-P370+P378q-P501c
Keep away from heat/sparks/open flames/hot surfaces. - No smoking. Keep container tightly closed. Ground/bond container and receiving equipment. Use explosion-proof electrical/ventilating/lighting/ equipment. Use only non-sparking tools. Take precautionary measures against static discharge. Wear protective gloves/protective clothing/eye protection/face protection. IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. In case of fire: Use CO2, dry chemical, or foam Dispose of contents/ container to an approved waste disposal plant