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18620-04-7

18620-04-7 Structure

18620-04-7 Structure
IdentificationBack 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
Chemical PropertiesBack Directory
[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
Safety DataBack Directory
[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
Hazard InformationBack 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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