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| | 4-Thioanisolemagnesium bromide Basic information |
| | 4-Thioanisolemagnesium bromide Chemical Properties |
| Boiling point | 65 °C | | density | 0.965 g/mL at 25 °C | | Fp | <1 °F | | storage temp. | 2-8°C | | form | Solution | | color | Clear yellow to brown | | InChI | 1S/C7H7S.BrH.Mg/c1-8-7-5-3-2-4-6-7;;/h3-6H,1H3;1H;/q;;+1/p-1 | | InChIKey | SSVQCUSLJVVRCA-UHFFFAOYSA-M | | SMILES | CSc1ccc([Mg]Br)cc1 |
| Hazard Codes | F,C,F+ | | Risk Statements | 11-14-19-34-12-37-40 | | Safety Statements | 16-26-36/37/39-45 | | RIDADR | UN 2924 3/PG 2 | | WGK Germany | 1 | | HazardClass | 3, 8 | | HS Code | 29309090 | | Storage Class | 3 - Flammable liquids | | Hazard Classifications | Acute Tox. 4 Oral
Carc. 2
Eye Dam. 1
Flam. Liq. 2
Skin Corr. 1B
STOT SE 3 |
| | 4-Thioanisolemagnesium bromide Usage And Synthesis |
| Chemical Properties | Tan liquid | | Uses | 4-Thioanisolemagnesium bromide can be used to prepare:
- 3,3-Ethylenedioxy-5a-hydroxy-11b-[4-(thiomethoxy)phenyl]-estr-9-en-17-one, a key intermediate for the synthesis of mifepristone analogs.
- (1S)-1,4-Anhydro-2,3,5,6-tetra-O-benzyl-1-C-[4-chloro-3-(4-methylthiobenzyl)-phenyl]-D-glucitol, a key intermediate for the synthesis of arylD-glucofuranosides as potent hSGLT2 and hSGLT1 inhibitors.
| | reaction suitability | reaction type: Grignard Reaction |
| | 4-Thioanisolemagnesium bromide Preparation Products And Raw materials |
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