Synonym: 1,1′-[1,2-Phenylenebis(methylene)]bis[1,1-bis(1,1-dimethylethyl)phosphine; 1,2-Bis(di-tert-butylphosphino)xylene; 1,2-Bis[(di-tert-butylphosphino)methyl]benzene
CAS Number: 121954-50-5
Empirical Formula (Hill Notation): C24H44P2
Molecular Weight: 394.55
MDL Number: MFCD03094573
Linear Formula: C6H4[CH2P[C(CH3)2]2]
Product Type: Chemical
This picture is provided solely for illustration purposes, it may have been created or edited with AI. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 631922-1G
| form |
solid |
| functional group |
phosphine |
| InChI |
1S/C24H44P2/c1-21(2,3)25(22(4,5)6)17-19-15-13-14-16-20(19)18-26(23(7,8)9)24(10,11)12/h13-16H,17-18H2,1-12H3 |
| InChI key |
SFCNPIUDAIFHRD-UHFFFAOYSA-N |
| Quality Level |
100  |
| reaction suitability |
reaction type: Buchwald-Hartwig Cross Coupling Reaction |
| |
reaction type: Heck Reaction |
| |
reaction type: Hiyama Coupling |
| |
reaction type: Negishi Coupling |
| |
reaction type: Sonogashira Coupling |
| |
reaction type: Stille Coupling |
| |
reaction type: Suzuki-Miyaura Coupling |
| |
reagent type: ligand |
| SMILES string |
CC(C)(C)P(Cc1ccccc1CP(C(C)(C)C)C(C)(C)C)C(C)(C)C |
| Application: |
DTBPMB may be used as a ligand for the palladium-catalyzed hydroesterification of styrene and vinyl acetate to form branched esters in the presence of polymeric sulfonic acids promoters. |
| General description: |
1,2-Bis(di-tert-butylphosphinomethyl)benzene (DTBPMB) is a bidentate phosphine ligand. DTBPMB in combination with Pd2(dba)3 (dba = trans,trans-dibenzylideneacetone) and a sulfonic acid can catalyze the methoxycarbonylation of ethane to form methyl propanoate. |
| Packaging: |
1, 5 g in glass bottle |
| RIDADR |
NONH for all modes of transport |
| WGK Germany |
WGK 3 |
| Flash Point(F) |
Not applicable |
| Flash Point(C) |
Not applicable |