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| 6-Bromohexanoic acid Chemical Properties |
| Melting point | 32-34 °C (lit.) | | Boiling point | 165-170 °C/20 mmHg (lit.) | | density | 1.3996 (rough estimate) | | refractive index | 1.4790 (estimate) | | Fp | 154 °F | | storage temp. | Inert atmosphere,2-8°C | | solubility | methanol: 0.1 g/mL, clear, colorless | | pka | 4.72±0.10(Predicted) | | form | Low Melting Crystals | | color | White to light orange | | BRN | 1749740 | | InChIKey | NVRVNSHHLPQGCU-UHFFFAOYSA-N | | CAS DataBase Reference | 4224-70-8(CAS DataBase Reference) | | NIST Chemistry Reference | Hexanoic acid, 6-bromo-(4224-70-8) | | EPA Substance Registry System | Hexanoic acid, 6-bromo- (4224-70-8) |
| Hazard Codes | C | | Risk Statements | 34 | | Safety Statements | 26-36/37/39-45-28A | | RIDADR | UN 3261 8/PG 2 | | WGK Germany | 3 | | F | 8 | | Hazard Note | Corrosive/Harmful | | TSCA | Yes | | HazardClass | 8 | | PackingGroup | III | | HS Code | 29159080 |
| 6-Bromohexanoic acid Usage And Synthesis |
| Organic Intermediate | 6-bromohexanoic acid, also called 6-bromohexanoic acid or 6-bromo-hexanoic acid, is an organobromine compound comprising hexanoic acid having a bromo substituent at the 6-position. 6-Bromohexanoic acid is used in the preparation of N-acylsulfonamides, diarylthioethers and 2-lithio-1,3-dithian. It is widely used as an intermediate in organic synthesis. Here, we introduced a method for making this compound.
| | Chemical Properties | White to light orange low melting crystals | | Uses | Employed in a direct preparation of N-acylsulfonamides on treatment with tosyl isocyanate (189278)1 and alkyl ketones from alkyl iodides and metallic strontium.2 | | Uses | 6-Bromohexanoic acid is used in the preparation of N-acylsulfonamides, diarylthioethers and 2-lithio-1,3-dithian. It is widely used as an intermediate in organic synthesis. | | Uses | 6-Bromohexanoic acid was used in the preparation of N-acylsulfonamides on treatment with tosyl isocyanate (189278) and alkyl ketones from alkyl iodides and metallic strontium. It was also used in the synthesis of anionic mitomycin C-dextran conjugate (MMC-D), 2-lithio-1,3-dithian and diaryl thioethers. | | Definition | ChEBI: An organobromine compound comprising hexanoic acid having a bromo substituent at the 6-position. | | Synthesis Reference(s) | Journal of the American Chemical Society, 72, p. 5137, 1950 DOI: 10.1021/ja01167a091 |
| 6-Bromohexanoic acid Preparation Products And Raw materials |
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