| Identification | Back Directory | [Name]
CHLORO(DI-2-NORBORNYLPHOSPHINO)(2-DIMETHYLAMINOMETHYLFERROCEN-1-YL)PALLADIUM(II) | [CAS]
614753-51-4 | [Synonyms]
CHLORO(DI-2-NORBORNYLPHOSPHINO)(2-DIMETHYLAMINOFERROCEN-1-YL)PALLADIUM(II)
chloro-2-(dimethylaminomethyl)-ferrocen-1-yl-(dinorbornylphosphine)palladium
Chloro(di-2-norbornylphosphino)(2-dimethylaminomethylferrocen-1-yl)palladium(Ⅱ)
CHLORO(DI-2-NORBORNYLPHOSPHINO)(2-DIMETHYLAMINOMETHYLFERROCEN-1-YL)PALLADIUM(II)
2-(Dimethylaminomethyl)ferrocen-1-yl-palladium(II) chloride dinorbornylphosphine
Chloro(di-2-norbornylphosphino)(2-diMethylaMinoMethylferrocen-1-yl)palladiuM(II),97%
2-(Dimethylaminomethyl)ferrocen-1-yl-palladium(II) chloride Dinorbornylphosphine Complex
Chloro(di-2-norbornylphosphino)(2-dimethylaminomethylferrocen-1-yl)palladium(II),min.97%
SK-CC02-A, Chloro-2-(dimethylaminomethyl)-ferrocen-1-yl-(dinorbornylphosphine)palladium
Chloro(di-2-norbornylphosphino)(2-dimethylaminomethylferrocen-1-yl)palladium(II), min. 97%
2-(Dimethylaminomethyl)ferrocen-1-yl-palladium(II) chloride Dinorbornylphosphine Complex >=97.0% (C) | [Molecular Formula]
C27H39ClFeNPPd 10* | [MDL Number]
MFCD05861622 | [MOL File]
614753-51-4.mol | [Molecular Weight]
606.3 |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H335-H319-H315 | [Precautionary statements ]
P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362 | [WGK Germany ]
3
| [F ]
10-21 | [HS Code ]
28439000 | [Safety Statements ]
羟基积雪草苷( madecassoside，MC)为伞形科植物积雪草 Centella asiaticaUrb.的干燥全草，外用及内服应用已有两千多年历史，为 2010 年版中国药典一部收载的常用中药。用于湿热黄疸、中暑腹泻、石淋血淋、痈肿疮毒、跌扑损伤等。积雪草总苷口服或外敷可有效治疗外伤、手术创伤、烧伤、瘢痕疙瘩及硬皮病等。三萜皂苷类成分羟基积雪草酸( madasiatic acid) 是积雪草中最重要的活性成分之一，研究表明 MC 具有广泛 的体内外药理活性，可降低胶原诱导的关节炎炎症反应，促进体外培养的人成 纤维细胞增殖，治疗或预防增生性瘢痕和瘢痕瘤作用以及保护心肌缺血再灌注 损伤等。此外，MC 还有抗抑郁作用，机理可能与降低脑单胺氧化酶的活性有 关;同时，MC对急性脊髓损伤大鼠神经元及慢性铝中毒致小鼠痴呆也具有保护 作用。 
图：积雪草
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| Questions And Answer | Back Directory | [Reaction]
- Efficient catalyst for the amination of aryl chlorides
- Catalyst used for the efficient synthesis of substituted biaryl anilines and biaryl phenols.
- Catalyst used for the direct vinylation, and difluorovinylation, of arylboronic acids.
- Catalyst used in the Heck coupling of vinyl phosphates.
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