Formaldehyde/isopropyl alcohol/sodium nitrite

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

On irradiation with UV light, 1-nitro-2-naphthaldehyde gets transformed into the corresponding nitroso acid. Application 1-Nitro-2-naphthaldehyde (NAA) may be used to prepare the precursors required for the preparation of

Application Reactant for: Preparation of acitretin analogs with antitumor activity Stereoselective synthesis of essential building blocks of phorboxazole A via hetero Diels-Alder and stereoselective hetero-Michael addition/equilibration Preparation

2-Ethylbutyraldehyde reacts with cyclohexanecarbaldehyde to form homoallylic alcohols . Application 2-Ethylbutyraldehyde has been used in the preparation of aldoximes using aqueous hydroxylamine .

2-Ethylbutyraldehyde reacts with cyclohexanecarbaldehyde to form homoallylic alcohols . Application 2-Ethylbutyraldehyde has been used in the preparation of aldoximes using aqueous hydroxylamine .

2-Hydroxy-3-nitrobenzaldehyde can be extracted from the leaves of Actephila merrilliana . Its molecule is planar.

2-Hydroxy-3-nitrobenzaldehyde can be extracted from the leaves of Actephila merrilliana . Its molecule is planar.

2-Hydroxy-5-methoxy-3-nitrobenzaldehyde

2-Hydroxy-5-nitrobenzaldehyde is a nitroaromatic compound used to prepare Schiff base ligands. The interaction of 2-hydroxy-5-nitrobenzaldehyde and chlorogenic acid (CHL) with the components of the rat hepatic glucose 6-phosphatase system was

2-Hydroxy-5-nitrobenzaldehyde is a nitroaromatic compound used to prepare Schiff base ligands. The interaction of 2-hydroxy-5-nitrobenzaldehyde and chlorogenic acid (CHL) with the components of the rat hepatic glucose 6-phosphatase system was

Application Building block used in the preparation of 5-aryloxazoles.