TRIPHENYL[2-(1H-TETRAZOL-5-YL)ETHYLPHOSPHONIUM BROMIDE
TRIPHENYL[2-(1H-TETRAZOL-5-YL)ETHYLPHOSPHONIUM BROMIDE
CAS: 160126-54-5
Molecular Formula: C21H20BrN4P
TRIPHENYL[2-(1H-TETRAZOL-5-YL)ETHYLPHOSPHONIUM BROMIDE - Names and Identifiers
| Name | TRIPHENYL[2-(1H-TETRAZOL-5-YL)ETHYLPHOSPHONIUM BROMIDE |
| Synonyms | TRIPHENYL[2-(1H-TETRAZOL-5-YL)ETHYLPHOSPHONIUM BROMIDE |
| CAS | 160126-54-5 |
TRIPHENYL[2-(1H-TETRAZOL-5-YL)ETHYLPHOSPHONIUM BROMIDE - Physico-chemical Properties
| Molecular Formula | C21H20BrN4P |
| Molar Mass | 439.288061 |
TRIPHENYL[2-(1H-TETRAZOL-5-YL)ETHYLPHOSPHONIUM BROMIDE - Introduction
TRIPHENYL[2-(1H-TETRAZOL-5-YL)ETHYLPHOSPHONIUM BROMIDE is an organic compound with the chemical formula C2H5PBrN4. It is a colorless solid, soluble in ether and alcohol solvents at room temperature, but insoluble in water.
TRIPHENYL[2-(1H-TETRAZOL-5-YL)ETHYLPHOSPHONIUM BROMIDE is commonly used as a catalyst and reaction intermediate in chemical synthesis. It has high stability and activity, and is widely used in organic synthesis reactions, such as amination reaction, olefin addition reaction and so on. In addition, it is also useful for C- N bond-forming reactions and substitution reactions in organic synthesis.
The preparation of TRIPHENYL[2-(1H-TETRAZOL-5-YL)ETHYLPHOSPHONIUM BROMIDE is usually prepared by reacting ethyl magnesium BROMIDE with tetrazolium chlorophosphine. During the reaction, it is necessary to control the reaction temperature and reaction time, and at the same time, it is necessary to pay attention to the nucleophilic nature of the reaction to ensure the purity and yield of the synthesized product.
Specific toxicity and risk data on TRIPHENYL[2-(1H-TETRAZOL-5-YL)ETHYLPHOSPHONIUM BROMIDE are limited with regard to safety. However, during use and operation, General laboratory safety procedures should be followed, such as wearing appropriate protective equipment (such as gloves, goggles, laboratory coats, etc.), avoiding contact with skin and eyes, avoid inhaling or swallowing. At the same time, the compound should be stored and disposed of properly to avoid reaction with other chemicals to prevent potential hazards.
TRIPHENYL[2-(1H-TETRAZOL-5-YL)ETHYLPHOSPHONIUM BROMIDE is commonly used as a catalyst and reaction intermediate in chemical synthesis. It has high stability and activity, and is widely used in organic synthesis reactions, such as amination reaction, olefin addition reaction and so on. In addition, it is also useful for C- N bond-forming reactions and substitution reactions in organic synthesis.
The preparation of TRIPHENYL[2-(1H-TETRAZOL-5-YL)ETHYLPHOSPHONIUM BROMIDE is usually prepared by reacting ethyl magnesium BROMIDE with tetrazolium chlorophosphine. During the reaction, it is necessary to control the reaction temperature and reaction time, and at the same time, it is necessary to pay attention to the nucleophilic nature of the reaction to ensure the purity and yield of the synthesized product.
Specific toxicity and risk data on TRIPHENYL[2-(1H-TETRAZOL-5-YL)ETHYLPHOSPHONIUM BROMIDE are limited with regard to safety. However, during use and operation, General laboratory safety procedures should be followed, such as wearing appropriate protective equipment (such as gloves, goggles, laboratory coats, etc.), avoiding contact with skin and eyes, avoid inhaling or swallowing. At the same time, the compound should be stored and disposed of properly to avoid reaction with other chemicals to prevent potential hazards.
Last Update：2024-04-10 22:29:15
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TRIPHENYL[2-(1H-TETRAZOL-5-YL)ETHYLPHOSPHONIUM BROMIDE
氯化锆(IV), REACTOR GRADE (METALS BASIS)
LABOTEST-BB LT00942758
LDN 193719 5-[6-(4-Methoxyphenyl)pyrazolo[1,5-a]pyrimidin-3-yl]quinoline
Isolongifolene
METHYLTRI-N-BUTYLPHOSPHONIUM IODIDE
KAEMPFEROL-3-O-GLUCOSIDE
AMMONIUM NICKEL(II) SULFATE HEXAHYDRATE
lithium perchlorate trihydrate, reagent grade
monosodiumdibutyrylcyclicamp
氯化锆(IV), REACTOR GRADE (METALS BASIS)
LABOTEST-BB LT00942758
LDN 193719 5-[6-(4-Methoxyphenyl)pyrazolo[1,5-a]pyrimidin-3-yl]quinoline
Isolongifolene
METHYLTRI-N-BUTYLPHOSPHONIUM IODIDE
KAEMPFEROL-3-O-GLUCOSIDE
AMMONIUM NICKEL(II) SULFATE HEXAHYDRATE
lithium perchlorate trihydrate, reagent grade
monosodiumdibutyrylcyclicamp