[1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]chloro[2-[[(2-methylphenyl)imino]methyl]phenolato](3-phenyl-1H-inden-1-ylidene)ruthenium
Chloro(1,3-dimesityl-2-imidazolidinylidene)(2-{(E)-[(2-methylphenyl)imino]methyl}phenolato-κO)(3-phenyl-1H-inden-1-ylidene)ruthenium
CAS: 934538-12-2
Molecular Formula: C50H48ClN3ORu
[1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]chloro[2-[[(2-methylphenyl)imino]methyl]phenolato](3-phenyl-1H-inden-1-ylidene)ruthenium - Names and Identifiers
[1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]chloro[2-[[(2-methylphenyl)imino]methyl]phenolato](3-phenyl-1H-inden-1-ylidene)ruthenium - Physico-chemical Properties
| Molecular Formula | C50H48ClN3ORu |
| Molar Mass | 843.47 |
| Appearance | solid |
| Color | red-brown |
[1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]chloro[2-[[(2-methylphenyl)imino]methyl]phenolato](3-phenyl-1H-inden-1-ylidene)ruthenium - Risk and Safety
| HS Code | 28439000 |
[1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]chloro[2-[[(2-methylphenyl)imino]methyl]phenolato](3-phenyl-1H-inden-1-ylidene)ruthenium - Introduction
[1,3-Bis (2,4, 6-trimethylphenyl)-2-imidazolidinylidene][2-[[(2-methylphenyl) imino] methyl] phenoyl] (3-phenyl-1H-inden-1-ylidene) scandium chloride is an organic complex with the chemical formula C46H48ClN4ORu. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
-Appearance: solid powder or crystal
-melting point: about 200-220 ℃
-Storage conditions: to avoid light, keep dry
Use:
-This compound is a catalyst commonly used in organic synthesis reactions such as redox reactions, carbonylation reactions, and haloalkylation reactions.
-Can be used for catalytic coupling reactions in organic synthesis, such as Suzuki reaction, Heck reaction, etc.
-It has important application value in the synthesis of some organic materials.
Method:
-The compound is usually obtained by synthetic chemical methods. A common synthetic method is to react the corresponding precursor with appropriate reagents under suitable conditions to produce the desired product.
Safety Information:
-The safety information and toxicity of this compound are not fully understood. General laboratory safety procedures should be followed during handling and use.
-May be irritating and toxic, avoid inhalation, contact with skin and eyes. Appropriate personal protective equipment.
-The compound should be stored to avoid contact with flammable substances.
-In the event of accidental exposure or ingestion, seek prompt medical attention and provide guidance on the safety data of the compound.
Nature:
-Appearance: solid powder or crystal
-melting point: about 200-220 ℃
-Storage conditions: to avoid light, keep dry
Use:
-This compound is a catalyst commonly used in organic synthesis reactions such as redox reactions, carbonylation reactions, and haloalkylation reactions.
-Can be used for catalytic coupling reactions in organic synthesis, such as Suzuki reaction, Heck reaction, etc.
-It has important application value in the synthesis of some organic materials.
Method:
-The compound is usually obtained by synthetic chemical methods. A common synthetic method is to react the corresponding precursor with appropriate reagents under suitable conditions to produce the desired product.
Safety Information:
-The safety information and toxicity of this compound are not fully understood. General laboratory safety procedures should be followed during handling and use.
-May be irritating and toxic, avoid inhalation, contact with skin and eyes. Appropriate personal protective equipment.
-The compound should be stored to avoid contact with flammable substances.
-In the event of accidental exposure or ingestion, seek prompt medical attention and provide guidance on the safety data of the compound.
Last Update：2024-04-10 22:29:15
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[1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]chloro[2-[[(2-methylphenyl)imino]methyl]phenolato](3-phenyl-1H-inden-1-ylidene)ruthenium
Benzenebutanoic acid, 3-methoxy-α,α-dimethyl-γ-oxo-, ethyl ester
2-吡啶甲酸, 6-氯-4-甲氧基-, 甲酯
CID 133665656
TpPa-1(COFs)
蛋白激酶仰制剂KT5720 抗生素 KT 5720
索拉非尼相关物质2
RESTRICTION ENDONUCLEASE NCI I FROM NEIS
3-羟基-N-(2-甲基苯基)-4-((2,4,5-三氯苯基)偶氮)萘-2-甲酰胺
1-(O-CHLOROPHENYL)PIPERAZINE HYDROCHLORIDE
Benzenebutanoic acid, 3-methoxy-α,α-dimethyl-γ-oxo-, ethyl ester
2-吡啶甲酸, 6-氯-4-甲氧基-, 甲酯
CID 133665656
TpPa-1(COFs)
蛋白激酶仰制剂KT5720 抗生素 KT 5720
索拉非尼相关物质2
RESTRICTION ENDONUCLEASE NCI I FROM NEIS
3-羟基-N-(2-甲基苯基)-4-((2,4,5-三氯苯基)偶氮)萘-2-甲酰胺
1-(O-CHLOROPHENYL)PIPERAZINE HYDROCHLORIDE