Comparison

Xantphos European Partner

Item no. TMO-T19936-1g
Manufacturer TargetMol
CASRN 161265-03-8
Amount 1 g
Quantity options 100 mg 1 g 500 mg 50 mg
Category
Type Molecules
Specific against other
Citations Song T, Park JE, Chung YK. Rhodium-Catalyzed Synthesis of Imines and Esters from Benzyl Alcohols and Nitroarenes: Change in Catalyst Reactivity Depending on the Presence or Absence of the Phosphine Ligand. J Org Chem. 2018 Apr 6;83(7):4197-4203. doi: 10.1021/acs.joc.8b00197. Epub 2018 Mar 19. PubMed PMID: 29536727.
Smiles CC1(C)C2=CC=CC(P(C3=CC=CC=C3)C3=CC=CC=C3)=C2OC2=C(C=CC=C12)P(C1=CC=CC=C1)C1=CC=CC=C1
ECLASS 10.1 32169090
ECLASS 11.0 32169090
UNSPSC 12000000
Alias 161265-03-8
Shipping Condition Cool pack
Available
Manufacturer - Targets
Others
Shipping Temperature
Cool pack
Storage Conditions
-20
Molecular Weight
578.62
Description
Xantphos, a ligand in the coupling reaction of Buchwald, Suzuki and others, is a metal chelating ligand that can be used to catalyze the reaction.
Pathways
Others
Bioactivity
Xantphos is an organophosphorus compound derived from the heterocycle xanthene.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 1 g
Available: In stock
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