1,3,5-Tris(m-iodophenyl)benzene
1,3,5-tris(3-iodophenyl)benzene
CAS: 855239-61-1
Molecular Formula: C24H15I3
1,3,5-Tris(m-iodophenyl)benzene - Names and Identifiers
| Name | 1,3,5-tris(3-iodophenyl)benzene |
| Synonyms | 1,3,5-Tris(m-iodophenyl)benzene 1,3,5-tris(3-iodophenyl)benzene 1,3,5-tris(m-iodophenyl)benzene 1,3,5-Tris(3-iodophenyl)benzene |
| CAS | 855239-61-1 |
| InChI | InChI=1S/C24H15I3/c25-22-7-1-4-16(13-22)19-10-20(17-5-2-8-23(26)14-17)12-21(11-19)18-6-3-9-24(27)15-18/h1-15H |
1,3,5-Tris(m-iodophenyl)benzene - Physico-chemical Properties
| Molecular Formula | C24H15I3 |
| Molar Mass | 684.09 |
| Density | 1.946 |
| Storage Condition | 2-8°C |
1,3,5-Tris(m-iodophenyl)benzene - Introduction
1,3,5-tris(3-iodophenyl)benzene is an organic compound whose chemical formula is C18H9I3. The following is a description of its nature, use, formulation and safety information:
Nature:
1,3,5-tris(3-iodophenyl)benzene is a solid compound whose crystal appears colorless to white, which is insoluble in water at room temperature and soluble in organic solvents such as methylene chloride and n-hexane. It has high thermal stability and electrochemical stability.
Use:
1,3,5-tris(3-iodophenyl)benzene are often used in organic synthesis reactions as interacting reagents and ligands for transition metal compounds. It is widely used in the research fields of organic photoelectric devices, photoelectric materials and organic electrochromic materials.
Preparation Method:
1,3,5-tris(3-iodophenyl)benzene are generally prepared by the reaction of iodinated phenyl compounds. The specific synthesis method can be carried out in various ways, for example, it can be carried out by diazotization reaction, reduction reaction or arylation reaction under alkaline conditions.
Safety Information:
1,3,5-tris(3-iodophenyl)benzene are generally relatively safe under normal conditions of use. However, due to the particularity of its chemical properties, certain safety procedures should be followed, such as wearing protective gloves, glasses and laboratory coats to prevent contact with skin and eyes. At the same time, it should be operated in a well-ventilated laboratory to avoid inhaling its volatile or dust. In case of accidental contact or inhalation, rinse immediately with plenty of water and seek medical help. When disposing of waste, follow the guidance of local environmental regulations.
Nature:
1,3,5-tris(3-iodophenyl)benzene is a solid compound whose crystal appears colorless to white, which is insoluble in water at room temperature and soluble in organic solvents such as methylene chloride and n-hexane. It has high thermal stability and electrochemical stability.
Use:
1,3,5-tris(3-iodophenyl)benzene are often used in organic synthesis reactions as interacting reagents and ligands for transition metal compounds. It is widely used in the research fields of organic photoelectric devices, photoelectric materials and organic electrochromic materials.
Preparation Method:
1,3,5-tris(3-iodophenyl)benzene are generally prepared by the reaction of iodinated phenyl compounds. The specific synthesis method can be carried out in various ways, for example, it can be carried out by diazotization reaction, reduction reaction or arylation reaction under alkaline conditions.
Safety Information:
1,3,5-tris(3-iodophenyl)benzene are generally relatively safe under normal conditions of use. However, due to the particularity of its chemical properties, certain safety procedures should be followed, such as wearing protective gloves, glasses and laboratory coats to prevent contact with skin and eyes. At the same time, it should be operated in a well-ventilated laboratory to avoid inhaling its volatile or dust. In case of accidental contact or inhalation, rinse immediately with plenty of water and seek medical help. When disposing of waste, follow the guidance of local environmental regulations.
Last Update：2024-04-10 22:29:15
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CAS: 855239-61-1
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View History
1,3,5-Tris(m-iodophenyl)benzene
N-[(S)-α-Ethyl-α-methylbenzyl]acetamide
52117-69-8
methyl 6-amino-5-bromo-2-methylnicotinate
(S)-1-(4-chlorophenyl)-7-isopropoxy-6-methoxy-2-(4-(methyl(((1r,4S)-4-(4-methyl-3-oxopiperazin-1-yl)cyclohexyl)methyl)amino)phenyl)-1,2-dihydroisoquinolin-3(4H)-one
4-hydroxy-2-oxo-N-(4-propoxyphenyl)-1,2-dihydroquinoline-3-carboxamide
propyl 4-(3-bromophenyl)-2-[(3-pyridinylcarbonyl)amino]-3-thiophenecarboxylate
benzyl 3-hydroxy-3-(trifluoroMethyl)azetidine-1-carboxylate
3-Bromo-5,8-dimethoxy-2-(4-methylphenylamino)-4-oxo-4H-1-benzothiopyran 1,1-dioxide
298-08-8
N-[(S)-α-Ethyl-α-methylbenzyl]acetamide
52117-69-8
methyl 6-amino-5-bromo-2-methylnicotinate
(S)-1-(4-chlorophenyl)-7-isopropoxy-6-methoxy-2-(4-(methyl(((1r,4S)-4-(4-methyl-3-oxopiperazin-1-yl)cyclohexyl)methyl)amino)phenyl)-1,2-dihydroisoquinolin-3(4H)-one
4-hydroxy-2-oxo-N-(4-propoxyphenyl)-1,2-dihydroquinoline-3-carboxamide
propyl 4-(3-bromophenyl)-2-[(3-pyridinylcarbonyl)amino]-3-thiophenecarboxylate
benzyl 3-hydroxy-3-(trifluoroMethyl)azetidine-1-carboxylate
3-Bromo-5,8-dimethoxy-2-(4-methylphenylamino)-4-oxo-4H-1-benzothiopyran 1,1-dioxide
298-08-8