Antifungal triazoles

Analysis Note Assay (GC, area%): &#8805 98.0 % (a/a) Melting range (lower value): &#8805 117 &#176C Melting range (upper value): &#8804 121 &#176C Identity (IR): passes test

Analysis Note Assay (GC, area%): &#8805 98.0 % (a/a) Melting range (lower value): &#8805 117 &#176C Melting range (upper value): &#8804 121 &#176C Identity (IR): passes test

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 Reagent for preparing the reactive acyl triazolides from carboxylic acids Reaction of unprotected glucose with acyl triazolide to the &#946-D-glucosyl ester Dehydrating agent which reacts with H 2 O 2 giving singlet oxygen, used

Other Notes Reagent for preparing the reactive acyl triazolides from carboxylic acids Reaction of unprotected glucose with acyl triazolide to the &#946-D-glucosyl ester Dehydrating agent which reacts with H 2 O 2 giving singlet oxygen, used

Application 1,2,4-Triazole sodium derivative (sodium-1,2,4-triazolide) may be used in chemical synthesis studies.

Application 1,2,4-Triazole sodium derivative (sodium-1,2,4-triazolide) may be used in chemical synthesis studies.

1,2,4-Triazole-3-carboxylic acid

Air stable organocatalyst for Baylis-Hillman transformation

Air stable organocatalyst for Baylis-Hillman transformation

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of rare and 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.