You Searched For: trans-Crotonyl+chloride


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Supplier: Thermo Scientific
Description: CAS No.: 625-35-4

SDS

Catalog Number: (8.20351.0025)
Supplier: Merck
Description: Crotonoyl chloride cis- and trans-mixture for synthesis, Sigma-Aldrich®
UOM: 1 * 25 mL

SDS


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Supplier: Apollo Scientific
Description: Crotonoyl chloride mixture of isomers 96%

Supplier: Thermo Scientific
Description: Crotonoyl chloride 90% remainder mainly cis-isomer, Technical Grade
Catalog Number: (8.00236.0100)
Supplier: Merck
Description: trans-Cinnamoyl chloride for synthesis, Sigma-Aldrich®
UOM: 1 * 100 mL

SDS


Supplier: Thermo Scientific
Description: trans-Cinnamoyl chloride ≥97%
Supplier: Apollo Scientific
Description: trans-3-(Trifluoromethyl)cinnamoyl chloride 97%

Catalog Number: (APOSOR924248-100G)
Supplier: Apollo Scientific
Description: trans-Cinnamoyl chloride 95%
UOM: 1 * 100 g


Catalog Number: (H32403.03)
Supplier: Thermo Scientific
Description: trans-3-(Trifluoromethyl)cinnamoyl chloride ≥99%
UOM: 1 * 1 g

Supplier: Thermo Scientific
Description: Cinnamoyl chloride predominantly trans 98%

SDS

Supplier: Thermo Scientific
Description: trans-Bis(triphenylphosphine)palladium(II) chloride (≥14.0% Pd)
Supplier: Thermo Scientific
Description: Appearance: Yellow to yellow-brown Liquid

SDS

Supplier: Apollo Scientific
Description: Tigloyl chloride

Supplier: Thermo Scientific
Description: trans-Bis(triphenylphosphine)palladium(II) chloride ≥99.95% (metals basis) Pd ≥ 14.7%, Premion®
Supplier: Thermo Scientific
Description: trans-Dichlorobis(triethylphosphine)palladium(II)

SDS

Catalog Number: (BOSSBS-13312R-HRP)
Supplier: Bioss
Description: GCDH is a 438 amino acid protein that localizes to the mitochondrial matrix and belongs to the acyl-CoA dehydrogenase family. Existing as a homotetramer, GCDH uses FAD as a cofactor to catalyze the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine and L-tryptophan metabolism. While GCDH exists as both a long and short isoform, only the long isoform is a functionally active protein. Defects in the gene encoding GCDH are the cause of glutaric acidemia type I (GA-I), an autosomal recessive disorder that is characterized by the accumulation of glutaconic acid and is associated with such symptoms as progressive dystonia and athetosis due to gliosis and neuronal loss in the basal ganglia.
UOM: 1 * 100 µl


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