666564

N-XantPhos

97%

Manufacturer: Sigma Aldrich

CAS Number: 261733-18-0

Synonym(S): NiXantphos, 4,6-Bis(diphenylphosphino)-10H-phenoxazine, 4,6-Bis(diphenylphosphino)phenoxazine

Select a Size

Pack Size SKU Availability Price
500 MG 666564-500-MG In Stock ₹ 11,636.88
1 G 666564-1-G In Stock ₹ 18,857.15

666564 - 500 MG

₹ 11,636.88

In Stock

Quantity

1

Base Price: ₹ 11,636.88

GST (18%): ₹ 2,094.638

Total Price: ₹ 13,731.518

Quality Level

100

Assay

97%

reaction suitability

reaction type: Buchwald-Hartwig Cross Coupling Reactionreaction type: Heck Reactionreaction type: Hiyama Couplingreaction type: Negishi Couplingreaction type: Sonogashira Couplingreaction type: Stille Couplingreaction type: Suzuki-Miyaura Couplingreagent type: ligandreaction type: Cross Couplings

mp

256-262 °C

functional group

phosphine

storage temp.

2-8°C

SMILES string

N1c2cccc(P(c3ccccc3)c4ccccc4)c2Oc5c1cccc5P(c6ccccc6)c7ccccc7

InChI

1S/C36H27NOP2/c1-5-15-27(16-6-1)39(28-17-7-2-8-18-28)33-25-13-23-31-35(33)38-36-32(37-31)24-14-26-34(36)40(29-19-9-3-10-20-29)30-21-11-4-12-22-30/h1-26,37H

InChI key

HSWZLYXRAOXOLL-UHFFFAOYSA-N

Related Products

Img

Sigma Aldrich

667218

97%...

Img

Sigma Aldrich

738611

97%...

Img

Sigma Aldrich

693049

--

Img

Sigma Aldrich

710342

97%...

Img

Sigma Aldrich

752231

97%...

Description

  • Application: N-XantPhos is a deprotonatable chelating aryldiphosphine ligand that can be used in:The preparation of Pd-NiXantphos catalyst system for the room temperature cross-coupling reactions of unactivated aryl chlorides.[1]The synthesis of cinchonine iridium(III) cyclometalated complex that exhibits luminescence and good quantum efficiency.[2]N-XantPhos and N-modified counterparts are also used in the preparation of rhodium based catalysts for hydroformylation reaction.[3]

SAFETY INFORMATION

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable