CAS 35059-50-8
:tert-butyl diazoacetate
Description:
Tert-butyl diazoacetate is an organic compound characterized by its diazo functional group, which is known for its reactivity in various chemical reactions, particularly in the formation of carbon-carbon bonds. It has a tert-butyl group, which contributes to its steric bulk and influences its reactivity. The compound is typically a colorless to pale yellow liquid and is soluble in organic solvents. Its structure includes a diazo group (-N=N-) attached to an acetate moiety, making it a useful reagent in organic synthesis, especially in the generation of carbenes. Tert-butyl diazoacetate is often employed in cyclopropanation reactions and other transformations that involve the generation of reactive intermediates. Due to the presence of the diazo group, it can be sensitive to heat and light, necessitating careful handling and storage under inert atmospheres. Safety precautions are essential when working with this compound, as diazo compounds can be hazardous and potentially explosive under certain conditions.
Formula:C6H10N2O2
InChI:InChI=1/C6H10N2O2/c1-6(2,3)10-5(9)4-8-7/h4H,1-3H3
SMILES:CC(C)(C)OC(=O)C=[N+]=[NH-]
Synonyms:- 1-Tert-Butoxy-2-Diazonioethenolate
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Found 5 products.
tert-Butyl Diazoacetate
CAS:Formula:C6H10N2O2Purity:95%Color and Shape:LiquidMolecular weight:142.1558tert-Butyl 2-diazoacetate
CAS:<p>tert-Butyl 2-diazoacetate</p>Formula:C6H10N2O2Purity:96%Color and Shape: clear. yellow liquidMolecular weight:142.16g/moltert-Butyl Diazoacetate, 85%
CAS:Controlled Product<p>Applications An intermediate in the production of Zolpidem metabolites<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Klupsch, F., et al.: Chem. Pharm. Bull., 54, 1318 (2006), Epple, R., et al.: Bioorg. Med. Chem. Lett., 16, 5488 (2006),<br></p>Formula:C6H10N2O2Purity:85%Color and Shape:NeatMolecular weight:142.16tert-Butyl diazoacetate
CAS:<p>Tert-Butyl diazoacetate is an ethyl diazoacetate that undergoes a copper-catalyzed alkylation with 4-acetamidobenzene sulfonyl azide. The reaction rate is dependent on the concentration of chloride, which is the only byproduct. This compound has been used in asymmetric synthesis of 4-formylbenzenesulfonyl azide and has shown to be a useful tool for organic chemists due to its size-exclusion chromatography properties. Tert-Butyl diazoacetate also reacts with styrene to produce unsaturated ketones such as salicylaldehyde, which can be further modified. Tert-Butyl diazoacetate is also an important bioactive molecule because it can be isolated from natural sources like horseradish or soybean sprouts.</p>Formula:C6H10N2O2Purity:Min. 95%Molecular weight:142.16 g/mol




