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| | Trichloroheptyl Stannane Basic information |
| Product Name: | Trichloroheptyl Stannane | | Synonyms: | MONO-N-HEPTYLTIN TRICHLORIDE;Trichloroheptyl Stannane;n-Heptyltin-trichloride;heptyl-tin trichloride;Trichloroheptyl Stannane (~80%);Mono-n-heptyltin trichloride, Purified;Stannane, trichloroheptyl-;n-Heptyltin trichlorid in Methanol | | CAS: | 59344-47-7 | | MF: | C7H15Cl3Sn | | MW: | 324.26 | | EINECS: | | | Product Categories: | Aliphatics | | Mol File: | 59344-47-7.mol |  |
| | Trichloroheptyl Stannane Chemical Properties |
| Boiling point | 282.6±9.0 °C(Predicted) | | storage temp. | Refrigerator | | solubility | Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly) | | form | Oil | | color | Colourless |
| | Trichloroheptyl Stannane Usage And Synthesis |
| Uses | An organotin compound of type MenSnCl3-n(CH2)mMe (n = 0-3, m = 0-7)
ed; SnMe3 causes a small upfield shift on the directly bonded C whereas other groups cause downfield shifts. | | Uses | An organotin compound of type MenSnCl3-n(CH2)mMe (n = 0-3, m = 0-7). The substituent effects of the SnMe3, SnMe2Cl, SnMeCl2, and SnCl3 groups on the C chemical shifts in the alkyl group were determined; SnMe3 causes a small upfield shift on the directly bonded C whereas other groups cause downfield shifts. |
| | Trichloroheptyl Stannane Preparation Products And Raw materials |
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