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Ohira-Bestmann Reagent Solution 50 ml  | >96%

AdipoGen Life Sciences

Used in the Seyferth-Gilbert homologation which is a chemical reaction of an aryl ketone or aldehyde with dimethyl- or diazomethyl-phosphonate and potassium tert-butoxide to give substituted alkynes.

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Ohira-Bestmann Reagent Solution 10 ml  | >96%

AdipoGen Life Sciences

Used in the Seyferth-Gilbert homologation which is a chemical reaction of an aryl ketone or aldehyde with dimethyl- or diazomethyl-phosphonate and potassium tert-butoxide to give substituted alkynes.

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Ohira-Bestmann Reagent 5 g  | >96%

AdipoGen Life Sciences

Used in the Seyferth-Gilbert homologation which is a chemical reaction of an aryl ketone or aldehyde with dimethyl- or diazomethyl-phosphonate and potassium tert-butoxide to give substituted alkynes.

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Ohira-Bestmann Reagent 1 g  | >96%

AdipoGen Life Sciences

Used in the Seyferth-Gilbert homologation which is a chemical reaction of an aryl ketone or aldehyde with dimethyl- or diazomethyl-phosphonate and potassium tert-butoxide to give substituted alkynes.

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3,8-Diamino-6-phenylphenanthridine 5 g  | >98%

AdipoGen Life Sciences

Phenyl-phenanthridine dye with a large pi-conjugated structure and strong luminescence. Used in the synthesis of rigid polyamides and fluorescent probes. DNA intercalator. Used as a chromatographic affinity ligand for the specific separation and purification of supercoiled plasmid DNA (pDNA). It has been investigated for its anti-tumor and anti-viral properties.

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3,8-Diamino-6-phenylphenanthridine 1 g  | >98%

AdipoGen Life Sciences

Phenyl-phenanthridine dye with a large pi-conjugated structure and strong luminescence. Used in the synthesis of rigid polyamides and fluorescent probes. DNA intercalator. Used as a chromatographic affinity ligand for the specific separation and purification of supercoiled plasmid DNA (pDNA). It has been investigated for its anti-tumor and anti-viral properties.

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(S,S)-(-)-1,4-Dimethoxy-2,3-butanediol 5 g  | >99%

AdipoGen Life Sciences

Building block for synthesis. For chiral auxiliary modification of LAH. Condensation of ester enolates and chiral imines to beta-lactams. Auxiliary, reactions of its acetal. Determination of the enantiomeric purity of ketones by acetal formation and 13C-NMR.

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