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341673-5G
1 1'-THIOCARBONYLDI-2(1H)-PYRIDONE 97% (C005B-004442)
Price: $318.81List Price: $354.24Application 1,1′-Thiocarbonyldi-2(1 H )-pyridone was used in the preparation of: thio-analogs of thioureas sulforaphane 2-furan-2-yl-3-hydroxy-6-isothiocyanato-chromen-4-one -
B301101-100g
1,1'-Thiocarbonyldi-2(1H)-pyridone (C007B-062801)
Price: $2,166.90List Price: $2,407.66application:1,1′-Thiocarbonyldi-2(1H)-pyridone was used in the preparation of:thio-analogs of thioureas,sulforaphane,2-furan-2-yl-3-hydroxy-6-isothiocyanato-chromen-4-one. -
B301101-1g
1,1'-Thiocarbonyldi-2(1H)-pyridone (C007B-062802)
Price: $119.25List Price: $132.50application:1,1′-Thiocarbonyldi-2(1H)-pyridone was used in the preparation of:thio-analogs of thioureas,sulforaphane,2-furan-2-yl-3-hydroxy-6-isothiocyanato-chromen-4-one. -
B301101-250mg
1,1'-Thiocarbonyldi-2(1H)-pyridone (C007B-062803)
Price: $69.80List Price: $77.56application:1,1′-Thiocarbonyldi-2(1H)-pyridone was used in the preparation of:thio-analogs of thioureas,sulforaphane,2-furan-2-yl-3-hydroxy-6-isothiocyanato-chromen-4-one. -
B301101-25g
1,1'-Thiocarbonyldi-2(1H)-pyridone (C007B-062804)
Price: $751.50List Price: $835.00application:1,1′-Thiocarbonyldi-2(1H)-pyridone was used in the preparation of:thio-analogs of thioureas,sulforaphane,2-furan-2-yl-3-hydroxy-6-isothiocyanato-chromen-4-one. -
B301101-5g
1,1'-Thiocarbonyldi-2(1H)-pyridone (C007B-062805)
Price: $314.08List Price: $348.98application:1,1′-Thiocarbonyldi-2(1H)-pyridone was used in the preparation of:thio-analogs of thioureas,sulforaphane,2-furan-2-yl-3-hydroxy-6-isothiocyanato-chromen-4-one. -
108472-100G
2 5-DIBROMOTHIOPHENE 95% (C005B-031827)
Price: $316.58List Price: $351.762,5-Dibromothiophene polymerizes by debromination with magnesium catalyzed by nickel compounds to form poly(2,5- thienylene) . Application 2,5-Dibromothiophene was used as starting reagent for the synthesis of α,α′-didecylquater-, -
108472-25G
2 5-DIBROMOTHIOPHENE 95% (C005B-031828)
Price: $155.32List Price: $172.572,5-Dibromothiophene polymerizes by debromination with magnesium catalyzed by nickel compounds to form poly(2,5- thienylene) . Application 2,5-Dibromothiophene was used as starting reagent for the synthesis of α,α′-didecylquater-, -
T290266-1g
2,2'-(5,5'-(thieno[3,2-b ]thiophene-2,5-diyl)bis(thiophene-5,2-diyl))bis(methan-1-yl-1-ylidene)dimalononitrile
Price: $5,254.95List Price: $5,838.832,2'-(5,5'-(thieno[3,2-b ]thiophene-2,5-diyl)bis(thiophene-5,2-diyl))bis(methan-1-yl-1-ylidene)dimalononitrile. -
T695635-250mg
2-(1-Propen-2-yl)thiophene (C007B-501162)
Price: $304.93List Price: $338.812-(1-Propen-2-yl)thiophene. -
T695635-5g
2-(1-Propen-2-yl)thiophene (C007B-501163)
Price: $1,765.82List Price: $1,962.032-(1-Propen-2-yl)thiophene. -
S553379-250MG
3 5-BIS-(3 3 5-TRIMETHYLCYCLOHEXYL)-TETRAHYDRO-1 3 5-THIADIAZINE-2)2H)-THIONE-
Price: $258.15List Price: $286.833 5-BIS-(3 3 5-TRIMETHYLCYCLOHEXYL)-TETRAHYDRO-1 3 5-THIADIAZINE-2)2H)-THIONE-