BIS(3 5 3' 5'-DIMETHOXYDIBENZYLIDENEACE&
- CAS NO.：811862-77-8
- Empirical Formula: 2C21H22O5.Pd
- Molecular Weight: 815.22
- MDL number: MFCD07369799
- SAFETY DATA SHEET (SDS)
- Update Date: 2023-07-26 16:38:34
What is BIS(3 5 3' 5'-DIMETHOXYDIBENZYLIDENEACE&?
The Uses of BIS(3 5 3' 5'-DIMETHOXYDIBENZYLIDENEACE&
suzuki reaction
The Uses of BIS(3 5 3' 5'-DIMETHOXYDIBENZYLIDENEACE&
Bis(3,5,3',5'-dimethoxydibenzylideneacetone)palladium(0) used as catalyst in pharmaceutical research.
General Description
Bis(3,5,3′,5′-dimethoxydibenzylideneacetone)palladium(0) is a non-phosphine based Pd(0) catalyst that can catalyze the Suzuki–Miyaura reaction of aryl chlorides with arylboronic acids with higher percentage conversion when compared to tris(dibenzylideneacetone)dipalladium(0) [Pd2(dba)3].
Properties of BIS(3 5 3' 5'-DIMETHOXYDIBENZYLIDENEACE&
| Melting point: | 170-178 °C(lit.) |
| storage temp. | under inert gas (nitrogen or Argon) at 2-8°C |
| form | Powder |
| color | Red-brown |
| Water Solubility | Insoluble in water. |
| InChI | InChI=1S/2C21H22O5.Pd/c2*1-23-18-9-15(10-19(13-18)24-2)5-7-17(22)8-6-16-11-20(25-3)14-21(12-16)26-4;/h2*5-14H,1-4H3;/b2*7-5+,8-6+; |
Safety information for BIS(3 5 3' 5'-DIMETHOXYDIBENZYLIDENEACE&
| Signal word | Warning |
| Pictogram(s) |
 Exclamation Mark Irritant GHS07 |
| GHS Hazard Statements |
H315:Skin corrosion/irritation H319:Serious eye damage/eye irritation H335:Specific target organ toxicity, single exposure;Respiratory tract irritation |
| Precautionary Statement Codes |
P261:Avoid breathing dust/fume/gas/mist/vapours/spray. P304+P340:IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing. P405:Store locked up. |
Computed Descriptors for BIS(3 5 3' 5'-DIMETHOXYDIBENZYLIDENEACE&
| InChIKey | RTGAJOPJZJDWAX-XVGSOSPHSA-N |
| SMILES | [CH](C1=CC(OC)=CC(OC)=C1)[CH]C(=O)[CH][CH]C1=CC(OC)=CC(OC)=C1.[CH](C1=CC(OC)=CC(OC)=C1)[CH]C(=O)[CH][CH]C1=CC(OC)=CC(OC)=C1.[Pd] |^1:0,11,14,15,26,37,40,41| |
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