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(H2IPr) (Cl) 2Ru=CH (o-iPrOC6H4)

(H2IPr) (Cl) 2Ru=CH (o-iPrOC6H4) is a highly efficient catalyst that can effectively promote the metathesis reaction of olefins. The compound exhibits excellent selectivity in the field of transition metal catalysts, is suitable for the synthesis of biologically active compounds, and shows potential application value in compound development.

Product Specifications

UNSPSC

12352300

Hazard Statement

H302, H312, H315, H319, H332, H335

Target

Biochemical Assay Reagents; Endogenous Metabolite

Type

Reference compound

Related Pathways

Metabolic Enzyme/Protease; Others

Applications

Metabolism-protein/nucleotide metabolism

Assay Protocol

https://www.medchemexpress.com/h2ipr-cl-2ru-ch-o-iproc6h4.html

Purity

98.0

Smiles

[Cl-][Ru+6]1([Cl-])(=[CH-2]C2=C(O1C(C)C)C=CC=C2)=[C-2]3N(CCN3C4=C(C(C)C)C=CC=C4C(C)C)C5=C(C(C)C)C=CC=C5C(C)C

Molecular Formula

C37H50Cl2N2ORu

Molecular Weight

710.78

Precautions

H302, H312, H315, H319, H332, H335

References & Citations

[1]A review of esomeprazole in the treatment of gastroesophageal reflux disease (GERD) Kalaitzakis E and Bjornsson ETherapeutics and Clinical Risk Management2007|[2]Esomeprazole increases airway surface liquid pH in primary Cystic Fibrosis epithelial cells|[3]A review of esomeprazole in the treatment of gastroesophageal reflux disease (GERD)

Shipping Conditions

Room Temperature

Storage Conditions

4°C (Powder, stored under nitrogen)

Product Datasheet

http://file.medchemexpress.com/batch_PDF/HY-W854275/H2IPr-Cl-2Ru-CH-o-iPrOC6H4-DataSheet-MedChemExpress.pdf

Product MSDS

http://file.medchemexpress.com/batch_PDF/HY-W854275/

Scientific Category

Reference compound1

Clinical Information

No Development Reported

CAS Number

[635679-24-2]

Available Sizes

Curated Selection

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