2-Chlorophenylzinc iodide solution 0.5M in THF
2-Chlorophenylzinc iodide
CAS: 148651-35-8
Molecular Formula: C6H4ClIZn
2-Chlorophenylzinc iodide solution 0.5M in THF - Names and Identifiers
2-Chlorophenylzinc iodide solution 0.5M in THF - Physico-chemical Properties
| Molecular Formula | C6H4ClIZn |
| Molar Mass | 303.84 |
| Density | 0.973g/mLat 25°C |
| Flash Point | 1°F |
| Exposure Limit | ACGIH: TWA 50 ppm; STEL 100 ppm (Skin)OSHA: TWA 200 ppm(590 mg/m3)NIOSH: IDLH 2000 ppm; TWA 200 ppm(590 mg/m3); STEL 250 ppm(735 mg/m3) |
| Storage Condition | 2-8°C |
| Sensitive | Air & Light Sensitive |
2-Chlorophenylzinc iodide solution 0.5M in THF - Risk and Safety
| Risk Codes | R11 - Highly Flammable R19 - May form explosive peroxides R22 - Harmful if swallowed R36/37/38 - Irritating to eyes, respiratory system and skin. R40 - Limited evidence of a carcinogenic effect R36/37 - Irritating to eyes and respiratory system. |
| Safety Description | S16 - Keep away from sources of ignition. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S33 - Take precautionary measures against static discharges. S36 - Wear suitable protective clothing. S36/37 - Wear suitable protective clothing and gloves. |
| UN IDs | UN 2056 3/PG 2 |
| WGK Germany | 1 |
| Hazard Class | 4.3 |
2-Chlorophenylzinc iodide solution 0.5M in THF - Introduction
2-Chlorophenylzinc iodide is an organic zinc compound with the chemical formula C6H4ClIZn. It is a colorless to pale yellow solid, soluble in non-polar solvents such as benzene and carbon disulfide. Its properties are similar to other organozinc compounds.
2-Chlorophenylzinc iodide is mainly used in organic synthesis as an important organic reagent. It can be used to catalyze chemical reactions, for example as a Grignard reagent in Grignard reactions, reacting alkynes with acyl compounds to form compounds with important biological activities. It can also be used in catalytic reduction reactions, carbazolylation reactions of olefins, and the like.
The preparation methods of 2-Chlorophenylzinc iodide are various. A common method is to synthesize by the reaction of zinc and 2-chlorophenyl iodide in a solvent. The specific preparation method can refer to the organic synthesis literature.
Regarding safety information, 2-Chlorophenylzinc iodide is an organometallic compound and should be operated under suitable laboratory conditions. It may be irritating to the skin, eyes and respiratory tract, so personal protective measures such as gloves, goggles and masks should be taken when using it. In addition, it should also be stored in a dry, cool place, away from fire and oxidants. Relevant safety operation regulations shall be followed in the experimental operation. When you encounter problems, you should consult a professional or consult relevant chemical safety information.
2-Chlorophenylzinc iodide is mainly used in organic synthesis as an important organic reagent. It can be used to catalyze chemical reactions, for example as a Grignard reagent in Grignard reactions, reacting alkynes with acyl compounds to form compounds with important biological activities. It can also be used in catalytic reduction reactions, carbazolylation reactions of olefins, and the like.
The preparation methods of 2-Chlorophenylzinc iodide are various. A common method is to synthesize by the reaction of zinc and 2-chlorophenyl iodide in a solvent. The specific preparation method can refer to the organic synthesis literature.
Regarding safety information, 2-Chlorophenylzinc iodide is an organometallic compound and should be operated under suitable laboratory conditions. It may be irritating to the skin, eyes and respiratory tract, so personal protective measures such as gloves, goggles and masks should be taken when using it. In addition, it should also be stored in a dry, cool place, away from fire and oxidants. Relevant safety operation regulations shall be followed in the experimental operation. When you encounter problems, you should consult a professional or consult relevant chemical safety information.
Last Update：2024-04-10 22:29:15
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