Methanesulfonato[di-t-butyl(n-butyl)phosphine](2'-amino-1,1'-biphenyl-2-yl)palladium(II) dichloromethane adduct
Methanesulfonato[di-t-butyl(n-butyl)phosphine](2'-amino-1,1'-biphenyl-2-yl)palladium(II) dichloromethane adduct
CAS: 2195390-27-1
Molecular Formula: C25H40NO3PPdS
Methanesulfonato[di-t-butyl(n-butyl)phosphine](2'-amino-1,1'-biphenyl-2-yl)palladium(II) dichloromethane adduct - Names and Identifiers
| Name | Methanesulfonato[di-t-butyl(n-butyl)phosphine](2'-amino-1,1'-biphenyl-2-yl)palladium(II) dichloromethane adduct |
| Synonyms | [P(t-Bu)2(n-Bu) Palladacycle Gen. 3] 2'-(Amino-κN)[1,1'-biphenyl]-2-yl-κC][butylbis(1,1-dimethylethyl)phosphine](methanesulfonato-κO)Palladium Methanesulfonato[di-t-butyl(n-butyl)phosphine](2'-amino-1,1'-biphenyl-2-yl)palladium(II) dichloromethane adduct |
| CAS | 2195390-27-1 |
Methanesulfonato[di-t-butyl(n-butyl)phosphine](2'-amino-1,1'-biphenyl-2-yl)palladium(II) dichloromethane adduct - Physico-chemical Properties
| Molecular Formula | C25H40NO3PPdS |
| Molar Mass | 572.05 |
Methanesulfonato[di-t-butyl(n-butyl)phosphine](2'-amino-1,1'-biphenyl-2-yl)palladium(II) dichloromethane adduct - Introduction
Methanesulfonato[di-t-butyl(n-butyl)phosphine](2 '-amino-1,1'-biphenyl-2-yl)palladium(II) dichlorometane adduct is an organometallic compound with the following chemical structure:
[CH3SO3CH3P(C4H9)(n-C4H9) Pd(II)(C6H4-NH2)(C6H4-2)]Cl2CH2Cl
The compound has the following properties:
1. Appearance: It is a solid substance, usually white or similar to white crystalline powder solid.
2. Thermal stability: It is relatively stable at room temperature, but may decompose when heated.
3. Solubility: It is soluble in some organic solvents, such as ethanol, dimethylformamide and dichloromethane.
Methanesulfonato[di-t-butyl(n-butyl) phosphate](2 '-amino-1,1'-biphenyl-2-yl)palladium(II) dichlorometane adduct has many uses in the field of organic synthesis:
1. Catalyst: It can be used as a catalyst in chemical reactions such as hydrogenation reaction, Suzuki coupling reaction and Heck reaction.
2. Organic Synthesis: it can promote the reduction of aromatic aldehyde alkene, the synthesis of heterocyclic and alkene carbonylation of organic synthesis reaction.
Methanesulfonato[di-t-butyl(n-butyl) phosphate](2 '-amino-1,1'-biphenyl-2-yl)palladium(II) dichlorometane adduct can be prepared as follows:
First, The Palladium Salt is reacted with methanesulfonic acid and additives in an appropriate solvent to form an activated palladium complex. Then 2 '-amino -1,1'-biphenyl-2-yl and di-tert-butyl (n-butyl) phosphine are added to the reaction system to form methanesulfonic acid [di-tert-butyl (n-butyl) phosphine](2 '-amino -1,1'-biphenyl-2-yl) palladium (II).
For safety information, Methanesulfonato[di-t-butyl(n-butyl)phosphine](2 '-amino-1,1'-biphenyl-2-yl)palladium(II) dichlorometane adduct is an organometallic compound, may be hazardous to health and the environment. Use should follow the safety procedures of the relevant laboratory and avoid contact with skin, eyes and respiratory tract.
[CH3SO3CH3P(C4H9)(n-C4H9) Pd(II)(C6H4-NH2)(C6H4-2)]Cl2CH2Cl
The compound has the following properties:
1. Appearance: It is a solid substance, usually white or similar to white crystalline powder solid.
2. Thermal stability: It is relatively stable at room temperature, but may decompose when heated.
3. Solubility: It is soluble in some organic solvents, such as ethanol, dimethylformamide and dichloromethane.
Methanesulfonato[di-t-butyl(n-butyl) phosphate](2 '-amino-1,1'-biphenyl-2-yl)palladium(II) dichlorometane adduct has many uses in the field of organic synthesis:
1. Catalyst: It can be used as a catalyst in chemical reactions such as hydrogenation reaction, Suzuki coupling reaction and Heck reaction.
2. Organic Synthesis: it can promote the reduction of aromatic aldehyde alkene, the synthesis of heterocyclic and alkene carbonylation of organic synthesis reaction.
Methanesulfonato[di-t-butyl(n-butyl) phosphate](2 '-amino-1,1'-biphenyl-2-yl)palladium(II) dichlorometane adduct can be prepared as follows:
First, The Palladium Salt is reacted with methanesulfonic acid and additives in an appropriate solvent to form an activated palladium complex. Then 2 '-amino -1,1'-biphenyl-2-yl and di-tert-butyl (n-butyl) phosphine are added to the reaction system to form methanesulfonic acid [di-tert-butyl (n-butyl) phosphine](2 '-amino -1,1'-biphenyl-2-yl) palladium (II).
For safety information, Methanesulfonato[di-t-butyl(n-butyl)phosphine](2 '-amino-1,1'-biphenyl-2-yl)palladium(II) dichlorometane adduct is an organometallic compound, may be hazardous to health and the environment. Use should follow the safety procedures of the relevant laboratory and avoid contact with skin, eyes and respiratory tract.
Last Update：2024-04-09 21:01:54
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Methanesulfonato[di-t-butyl(n-butyl)phosphine](2'-amino-1,1'-biphenyl-2-yl)palladium(II) dichloromethane adduct
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C.I. 13011 (Free acid)
N-Succinyl-Ala-Ala-Val-Ala P-Nitroanilide
7-Oxabicyclo[4.1.0]heptan-3-ylmethyl acrylate
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BENZYL 3-(4-(N-BENZYLOXYCARBONXYL-6-AMINOCAPROYLOXY)PHENYL)PROPIONATE
(3-METHYLPYRIDIN-2-YL)BORONIC ACID PINACOL ESTER
RESTRICTION ENDONUCLEASE NCI I
2-乙氧基苯基异硫氰酸酯
3-[(E)-[[(1R,2R)-2-[[(1S)-1-[(二甲氨基)羰基]-2,2-二甲基丙基]硫脲基]环己基]亚氨基]甲基]-5-(叔丁基)-4-羟基苯基新戊酸酯
C.I. 13011 (Free acid)