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| | 1-CHLORO-3-IODOPROPANE Basic information |
| | 1-CHLORO-3-IODOPROPANE Chemical Properties |
| Boiling point | 170-172 °C (lit.) | | density | 1.904 g/mL at 25 °C (lit.) | | vapor density | 6.8 (vs air) | | vapor pressure | 2 mm Hg ( 20 °C) | | refractive index | n20/D 1.548(lit.) | | Fp | >230 °F | | storage temp. | Keep in dark place,Inert atmosphere,2-8°C | | solubility | Difficult to mix. | | form | Liquid | | Specific Gravity | 1.904 | | color | Clear light yellow or light pink to orange | | Sensitive | Light Sensitive | | BRN | 1731115 | | CAS DataBase Reference | 6940-76-7(CAS DataBase Reference) | | EPA Substance Registry System | Propane, 1-chloro-3-iodo- (6940-76-7) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 3 | | F | 8-10 | | TSCA | Yes | | HS Code | 29037990 |
| | 1-CHLORO-3-IODOPROPANE Usage And Synthesis |
| Chemical Properties | CLEAR SLIGHTLY YELLOWISH TO LIGHT PINK LIQUID | | Uses | 1-Chloro-3-iodopropane has been used in the synthesis of N-[4-[5-(2,4-diamino-6-oxo-1,6-dihydropyrimidin-5-yl)-2-(2,2,2-trifluoroacetyl)pentyl]benzoyl]-L-glutamic acid, an inhibitor of glycinamide ribonucleotide transformylase (GAR Tfase) and aminoimidazole carboxamide ribonucleotide transformylase (AICAR Tfase), interesting proton sponge type molecule quino[7,8-h]quinoline. | | General Description | 1-Chloro-3-iodopropane undergoes asymmetric α-alkylation with N-sulfinyl imidates to yield 2-substituted N-tert-butanesulfinyl-5-chloropentanimidates. Electroreduction of 1-chloro-3-iodopropane at glassy carbon electrode in dimethylformamide containing tetra-n-butylammonium perchlorate has been investigated by cyclic voltammetry. It also participates in conjugate addition of alkyl iodides to α,β-unsaturated nitriles in water. |
| | 1-CHLORO-3-IODOPROPANE Preparation Products And Raw materials |
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