Di-tert-butylphenylphosphine, 97%

Name: Di-tert-butylphenylphosphine, 97% | 32673-25-9
Brand: J&K Chemical
SKU: JK947694_25_G
Price: 333.16 USD
Availability: OutOfStock

Cat. No JK947694_25_G

Vendor: J&K Chemical

Product Information

Product Name

Di-tert-butylphenylphosphine, 97%

Brand Name

J&K

Product Number

947694

CAS

32673-25-9

Molecular Formula

C14H23P

Molecular Weight

222.31

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

316378

IUPAC Name

ditert-butyl(phenyl)phosphane

InChI Key

XOJNEFQLMRCOMS-UHFFFAOYSA-N

SMILES

CC(C)(C)P(C1=CC=CC=C1)C(C)(C)C

Properties

Boiling Point

286.4

Safety Information

Storage Condition

Store at 2-8℃

References

Reaction-conditioned generative model for catalyst design and optimization with CatDRX

Publication Name: Communications Chemistry

Publication Date: 2025-10-23

DOI: 10.1038/s42004-025-01732-7

Coupling of Trifluoromethylarenes and Boronic Acids

Publication Name: Synfacts

Publication Date: 2021-10-19

DOI: 10.1055/s-0041-1737054

The emergence of Pd-mediated reversible oxidative addition in cross coupling, carbohalogenation and carbonylation reactions

Publication Name: Nature Catalysis

Publication Date: 2019-10-07

DOI: 10.1038/s41929-019-0361-0

Retaining Alkyl Nucleophile Regiofidelity in Transition-Metal-Mediated Cross-Couplings to Aryl Electrophiles

Publication Name: Synthesis

Publication Date: 2018-09-10

DOI: 10.1055/s-0037-1609941

Di- tert -butyl(N-pyrrolyl)phosphane,-sulfide, and-selenide, studied by multinuclear magnetic resonance

Publication Name: Fresenius' Journal of Analytical Chemistry

Publication Date: 1997-02-28

DOI: 10.1007/s002160050198

Di-tert-butylphenylphosphine, 97%

Product Information

General Information

Properties

Safety Information

References

Reaction-conditioned generative model for catalyst design and optimization with CatDRX

Coupling of Trifluoromethylarenes and Boronic Acids

The emergence of Pd-mediated reversible oxidative addition in cross coupling, carbohalogenation and carbonylation reactions

Retaining Alkyl Nucleophile Regiofidelity in Transition-Metal-Mediated Cross-Couplings to Aryl Electrophiles

Di- tert -butyl(N-pyrrolyl)phosphane,-sulfide, and-selenide, studied by multinuclear magnetic resonance