[2,9,16,23-tetrachloro-29H,31H-phthalocyaninato-N29,N30,N31,N32]-, (SP-4-1)-Copper
[2,9,16,23-tetrachloro-29H,31H-phthalocyaninato(2-)-N29,N30,N31,N32]copper
CAS: 16040-69-0
Molecular Formula: C32H12Cl4CuN8
[2,9,16,23-tetrachloro-29H,31H-phthalocyaninato-N29,N30,N31,N32]-, (SP-4-1)-Copper - Names and Identifiers
[2,9,16,23-tetrachloro-29H,31H-phthalocyaninato-N29,N30,N31,N32]-, (SP-4-1)-Copper - Physico-chemical Properties
| Molecular Formula | C32H12Cl4CuN8 |
| Molar Mass | 713.85 |
[2,9,16,23-tetrachloro-29H,31H-phthalocyaninato-N29,N30,N31,N32]-, (SP-4-1)-Copper - Introduction
[2,9, 16,23-tetrachloro-29h, 31H-phthalocyaninato(2-)-N29,N30,N31,N32]copper is a copper complex containing a phthalocyanine ligand. The following is a description of its nature, use, preparation and safety information:
1. Nature:
[2,9, 16,23-tetrachloro-29h, 31H-phthalocyaninato(2-)-N29,N30,N31,N32]copper is a dark blue solid with high solubility in solvents. It is a high absorbance compound that absorbs electromagnetic radiation in the visible and near-infrared regions. The complexes can undergo electron transfer in redox reactions.
2. Use:
[2,9, 16,23-tetrachloro-29h, 31H-phthalocyaninato(2-)-N29,N30,N31,N32]copper has certain application value in the field of chemistry and material science. It can be used as catalysts, dyes, sensors, Analytical reagents and fluorescent probes and other applications.
3. Preparation method:
The common method for preparing [2,9, 16,23-tetrachloro-29h, 31H-phthalocyaninato(2-)-N29,N30,N31,N32]copper is by reacting phthalocyanine ligand and copper salt, the target product can be purified by crystallization or separation and purification after the reaction is carried out in a suitable solvent.
4. Safety Information:
The complex is an organometallic compound with certain toxicity. Necessary personal protective equipment such as protective gloves, goggles, and air exhaust systems outside the laboratory should be worn during operation. Avoid contact with skin and inhalation of its powder. At the same time, according to local regulations, storage and disposal must comply with relevant safety regulations.
1. Nature:
[2,9, 16,23-tetrachloro-29h, 31H-phthalocyaninato(2-)-N29,N30,N31,N32]copper is a dark blue solid with high solubility in solvents. It is a high absorbance compound that absorbs electromagnetic radiation in the visible and near-infrared regions. The complexes can undergo electron transfer in redox reactions.
2. Use:
[2,9, 16,23-tetrachloro-29h, 31H-phthalocyaninato(2-)-N29,N30,N31,N32]copper has certain application value in the field of chemistry and material science. It can be used as catalysts, dyes, sensors, Analytical reagents and fluorescent probes and other applications.
3. Preparation method:
The common method for preparing [2,9, 16,23-tetrachloro-29h, 31H-phthalocyaninato(2-)-N29,N30,N31,N32]copper is by reacting phthalocyanine ligand and copper salt, the target product can be purified by crystallization or separation and purification after the reaction is carried out in a suitable solvent.
4. Safety Information:
The complex is an organometallic compound with certain toxicity. Necessary personal protective equipment such as protective gloves, goggles, and air exhaust systems outside the laboratory should be worn during operation. Avoid contact with skin and inhalation of its powder. At the same time, according to local regulations, storage and disposal must comply with relevant safety regulations.
Last Update：2024-04-09 21:11:58
![[2,9,16,23-tetrachloro-29H,31H-phthalocyaninato-N29,N30,N31,N32]-, (SP-4-1)-Copper](http://res.chembk.com/assets/images/structure/16040-69-0.gif)
Supplier List
View History
[2,9,16,23-tetrachloro-29H,31H-phthalocyaninato-N29,N30,N31,N32]-, (SP-4-1)-Copper
3-(2,3-Difluorophenyl)acrylic acid
1,3-Dioxane, 2-(2-bromo-5-methoxyphenyl)-
Ethyl m-trifluoromethylbenzoate
(3S,8aα)-3β-Isopropyloctahydropyrrolo[1,2-a]pyrazine-1,4-dione
4-(7-tert-butyl-4-oxo-3,4,5,6,7,8-hexahydro[1]benzothieno[2,3-d]pyrimidin-2-yl)phenyl benzenesulfonate
Acetamide, 2,2,2-trifluoro-N-(7-nitro-9H-fluoren-2-yl)-
5-(1,3-BENZODIOXOL-5-YLMETHYL)-3-METHYL-1,3-THIAZOLANE-2,4-DIONE
1-methyl-4-[1-(6-methylpyridin-2-yl)-1H-imidazole-4-carbonyl]piperazine
cyclopentyl 4-[3-chloro-4-hydroxy-5-(methyloxy)phenyl]-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate
3-(2,3-Difluorophenyl)acrylic acid
1,3-Dioxane, 2-(2-bromo-5-methoxyphenyl)-
Ethyl m-trifluoromethylbenzoate
(3S,8aα)-3β-Isopropyloctahydropyrrolo[1,2-a]pyrazine-1,4-dione
4-(7-tert-butyl-4-oxo-3,4,5,6,7,8-hexahydro[1]benzothieno[2,3-d]pyrimidin-2-yl)phenyl benzenesulfonate
Acetamide, 2,2,2-trifluoro-N-(7-nitro-9H-fluoren-2-yl)-
5-(1,3-BENZODIOXOL-5-YLMETHYL)-3-METHYL-1,3-THIAZOLANE-2,4-DIONE
1-methyl-4-[1-(6-methylpyridin-2-yl)-1H-imidazole-4-carbonyl]piperazine
cyclopentyl 4-[3-chloro-4-hydroxy-5-(methyloxy)phenyl]-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate