Iron(II) trifluoromethanesulfonate
Iron(II) trifluoromethanesulfonate
CAS: 59163-91-6
Molecular Formula: C2F6FeO6S2
Iron(II) trifluoromethanesulfonate - Names and Identifiers
| Name | Iron(II) trifluoromethanesulfonate |
| Synonyms | IRON(II) TRIFLUO Iron(II) triflate Iron trifluoroMethanesulfonate Iron(Ⅱ) trifluoroMethanesulfonate Iron(II) trifluoromethanesulfonate Iron bis(trifluoroMethanesulfonate) iron(2+) bis(trifluoromethanesulfonate) Iron(II) trifluoroMethanesulfonate (Iron triflate) Fe(CF3SO3)2 |
| CAS | 59163-91-6 |
| InChI | InChI=1/2CHF3O3S.Fe/c2*2-1(3,4)8(5,6)7;/h2*(H,5,6,7);/q;;+2/p-2 |
Iron(II) trifluoromethanesulfonate - Physico-chemical Properties
| Molecular Formula | C2F6FeO6S2 |
| Molar Mass | 353.98 |
| Melting Point | >300°C |
| Appearance | White powder |
| Color | off-white to brown |
| Storage Condition | Inert atmosphere,Room Temperature |
| Stability | hygroscopic |
| MDL | MFCD08460524 |
Iron(II) trifluoromethanesulfonate - Risk and Safety
| Hazard Symbols | C - Corrosive |
| Risk Codes | 34 - Causes burns |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S27 - Take off immediately all contaminated clothing. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
| UN IDs | UN 3260 8 / PGII |
| WGK Germany | 3 |
Iron(II) trifluoromethanesulfonate - Introduction
Iron(II) trifluoromethanesulfonate is an inorganic compound with the chemical formula Fe(CF3SO3)2. Its nature mainly includes the following aspects:
1. Appearance: Iron(II) trifluoromethanesulfonate as a colorless crystalline solid.
2. Storage and stability: Iron(II) trifluoromethanesulfonate is relatively stable at room temperature, but is sensitive to humidity and oxygen.
3. Solubility: Iron(II) trifluoromethanesulfonate is soluble in water, alcohols, ethers and chloride solutions.
About its use:
1. catalyst: Iron(II) trifluoromethanesulfonate is often used as a catalyst in organic synthesis, such as catalytic halogenated hydrocarbon alcoholization reaction, amination reaction, etc.
2. Material synthesis: Iron(II) trifluoromethanesulfonate can be used as a synthetic intermediate for some organic compounds, such as the preparation of certain complexes.
3. Others: Iron(II) trifluoromethanesulfonate also has potential applications in electrochemical and energy storage materials.
About its preparation method:
Iron(II) trifluoromethanesulfonate are generally prepared by reacting iron (II) chloride with sodium trifluoromethanesulfonate, and the resulting product is crystallized to obtain a pure product.
About safety information:
Iron(II) trifluoromethanesulfonate are generally relatively safe under normal conditions of use, but the following general safety precautions must be observed:
1. Avoid contact with skin: Avoid direct contact with Iron(II) trifluoromethanesulfonate solution or solid to prevent irritation or allergic reactions.
2. avoid inhalation: in the operation should pay attention to avoid inhalation of iron (II) trifluoromethanesulfonate of dust or gas, in order to prevent damage to the respiratory system.
3. Storage and handling: Iron(II) trifluoromethanesulfonate should be stored in a dry, well-ventilated place to avoid exposure to high humidity.
1. Appearance: Iron(II) trifluoromethanesulfonate as a colorless crystalline solid.
2. Storage and stability: Iron(II) trifluoromethanesulfonate is relatively stable at room temperature, but is sensitive to humidity and oxygen.
3. Solubility: Iron(II) trifluoromethanesulfonate is soluble in water, alcohols, ethers and chloride solutions.
About its use:
1. catalyst: Iron(II) trifluoromethanesulfonate is often used as a catalyst in organic synthesis, such as catalytic halogenated hydrocarbon alcoholization reaction, amination reaction, etc.
2. Material synthesis: Iron(II) trifluoromethanesulfonate can be used as a synthetic intermediate for some organic compounds, such as the preparation of certain complexes.
3. Others: Iron(II) trifluoromethanesulfonate also has potential applications in electrochemical and energy storage materials.
About its preparation method:
Iron(II) trifluoromethanesulfonate are generally prepared by reacting iron (II) chloride with sodium trifluoromethanesulfonate, and the resulting product is crystallized to obtain a pure product.
About safety information:
Iron(II) trifluoromethanesulfonate are generally relatively safe under normal conditions of use, but the following general safety precautions must be observed:
1. Avoid contact with skin: Avoid direct contact with Iron(II) trifluoromethanesulfonate solution or solid to prevent irritation or allergic reactions.
2. avoid inhalation: in the operation should pay attention to avoid inhalation of iron (II) trifluoromethanesulfonate of dust or gas, in order to prevent damage to the respiratory system.
3. Storage and handling: Iron(II) trifluoromethanesulfonate should be stored in a dry, well-ventilated place to avoid exposure to high humidity.
Last Update：2024-04-10 22:40:09
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Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
QQ: 2881950922
Wechat: 18621343501
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Spot supply
Product Name: Iron trifluoromethanesulfonate Visit Supplier Webpage Request for quotationCAS: 59163-91-6
Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
QQ: 495145328
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View History
Iron(II) trifluoromethanesulfonate
Pyridine, 2-chloro-5-[5-[[(4-chlorophenyl)methyl]thio]-4-[3-(trifluoromethyl)phenyl]-4H-1,2,4-triazol-3-yl]-
(Z)-2-chloro-3-dimethoxyphosphoryloxy-N,N-dimethyl-but-2-enamide
噻·异乳油
氮-(叔丁基二甲基硅基)邻苯二甲酰亚胺
3-甲基哌啶-4-羧酸乙酯盐酸盐
甲基4-(1-氨基乙基)苯甲酸酯盐酸盐
N-[3-[[5-(4-氯苯基)-1H-吡咯并[2,3-B]吡啶-3-基]羰基]-2,4-二氟苯基]-1-丙磺酰胺
HS-PEG3-CH2CH2NH2·HCl
2-(3-甲氧苯基)-7-甲基-3-咪唑并[3,2-A]吡啶甲醛
Pyridine, 2-chloro-5-[5-[[(4-chlorophenyl)methyl]thio]-4-[3-(trifluoromethyl)phenyl]-4H-1,2,4-triazol-3-yl]-
(Z)-2-chloro-3-dimethoxyphosphoryloxy-N,N-dimethyl-but-2-enamide
噻·异乳油
氮-(叔丁基二甲基硅基)邻苯二甲酰亚胺
3-甲基哌啶-4-羧酸乙酯盐酸盐
甲基4-(1-氨基乙基)苯甲酸酯盐酸盐
N-[3-[[5-(4-氯苯基)-1H-吡咯并[2,3-B]吡啶-3-基]羰基]-2,4-二氟苯基]-1-丙磺酰胺
HS-PEG3-CH2CH2NH2·HCl
2-(3-甲氧苯基)-7-甲基-3-咪唑并[3,2-A]吡啶甲醛