| Identification | Back Directory | [Name]
4-THIOANISOLEMAGNESIUM BROMIDE | [CAS]
18620-04-7 | [Synonyms]
emag
4-ThioanisoL
emagnesium bromide
4-THIOANISOLEMAGNESIUM BROMIDE
4-(Methylthio)phenylmagnesium bromide
p-(Methylthio)phenylmagnesium bromide
Magnesium,bromo[4-(methylthio)phenyl]-
magnesium,methylsulfanylbenzene,bromide
4-thioanisolemagnesium bromide solution
4-Thioanisolemagnesium bromide,0.5M solutionin THF
4-Thioanisolemagnesium bromide solution 0.5M in THF
4-(Methylsulfanyl)phenylmagnesium bromidee, 0.5 M in THF
4-ThioanisoleMagnesiuM broMide, 0.5 M solution in THF, SpcSeal
4-ThioanisoleMagnesiuM broMide, 0.5 M solution in THF, J&KSeal
4-Thioanisolemagnesium bromide, 0.5M solution in THF, AcroSeal
4-THIOANISOLEMAGNESIUM BROMIDE, 0.5M SOLUT TION IN TETRAHYDROFURAN
4-Thioanisolemagnesium bromide, 0.5M solution in THF, AcroSeal&trade | [Molecular Formula]
C7H7BrMgS | [MDL Number]
MFCD00672010 | [MOL File]
18620-04-7.mol | [Molecular Weight]
227.4 |
| Hazard Information | Back Directory | [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 aryl?D-glucofuranosides as potent hSGLT2 and hSGLT1 inhibitors.
| [reaction suitability]
reaction type: Grignard Reaction |
|
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