Kjeldahl Buffers and Reagents
OBORO LABS INC CAS# 1360926-56-2. 250 mg.
CAS# 1360926-56-2. 250 mg. OCO-Trianionic-pincer tungsten(VI)-tert-butyl-alkylidyne Veige Catalyst. IUPAC Name: (2,2-dimethylpropylidyne)bis(tetrahydrofuran); [3,3'-bis(1,1-dimethylethyl)[1,1':3',1''-terphenyl]-2,2''-diolato(3-)-κC²',κO²,κO²'']tungsten
OBORO LABS INC CAS# 1933506-99-0. 1 g. OCO-tethered-alkylidene tungsten(VI)-tert-butylacetylene. 2nd Generation-Veige Catalyst. IUPAC Name: N/A
CAS# 1933506-99-0. 1 g. OCO-tethered-alkylidene tungsten(VI)-tert-butylacetylene. 2nd Generation-Veige Catalyst. IUPAC Name: N/A
OBORO LABS INC CAS# 1933506-99-0. 100 mg. OCO-tethered-alkylidene tungsten(VI)-tert-butylacetylene. 2nd Generation-Veige Catalyst. IUPAC Name: N/A
CAS# 1933506-99-0. 100 mg. OCO-tethered-alkylidene tungsten(VI)-tert-butylacetylene. 2nd Generation-Veige Catalyst. IUPAC Name: N/A
OBORO LABS INC CAS# 1933506-99-0. 250 mg. OCO-tethered-alkylidene tungsten(VI)-tert-butylacetylene. 2nd Generation-Veige Catalyst. IUPAC Name: N/A
CAS# 1933506-99-0. 250 mg. OCO-tethered-alkylidene tungsten(VI)-tert-butylacetylene. 2nd Generation-Veige Catalyst. IUPAC Name: N/A
OBORO LABS INC CAS# 1360926-56-2. 100 mg.
CAS# 1360926-56-2. 100 mg. OCO-Trianionic-pincer tungsten(VI)-tert-butyl-alkylidyne Veige Catalyst. IUPAC Name: (2,2-dimethylpropylidyne)bis(tetrahydrofuran); [3,3'-bis(1,1-dimethylethyl)[1,1':3',1''-terphenyl]-2,2''-diolato(3-)-κC²',κO²,κO²'']tungsten
OBORO LABS INC CAS# 1933506-99-0. 10 g. OCO-tethered-alkylidene tungsten(VI)-tert-butylacetylene. 2nd Generation-Veige Catalyst. IUPAC Name: N/A
CAS# 1933506-99-0. 10 g. OCO-tethered-alkylidene tungsten(VI)-tert-butylacetylene. 2nd Generation-Veige Catalyst. IUPAC Name: N/A
OBORO LABS INC CAS# 1933506-99-0. 5 g. OCO-tethered-alkylidene tungsten(VI)-tert-butylacetylene. 2nd Generation-Veige Catalyst. IUPAC Name: N/A
CAS# 1933506-99-0. 5 g. OCO-tethered-alkylidene tungsten(VI)-tert-butylacetylene. 2nd Generation-Veige Catalyst. IUPAC Name: N/A
OBORO LABS INC VEIGE CATALYST 1
The trianionic pincer tungsten-alkylidyne Veige Catalyst is used in the synthesis of cyclic polymers. The Veige Catalyst will polymerize alkynes to produce cyclic polyacetylenes. The metal carbon bond coupled with a strained trianionic pincer ligand creates a highly reactive complex that will react with most unsaturated substrates. The ligands are specifically designed to provide a unique coordination environment, influencing the molecule's properties and potential applications. The presence of tetrahydrofuran ligands further enhances its solubility and compatibility in organic solvents, expanding its applicability in diverse chemical processes. ApplicationsThe distinctive structure of the Veige Catalyst makes it a promising candidate for various catalytic applications.
Sigma Organic Chemistry White-Clark catalyst | 100MG | 2226663-68-7
White-Clark catalyst, 100MG
About This Item:
UNSPSC Code: 12352200
Storage: room temp
