ChemicalBook > CAS DataBase List > 6-Methyl-8-methylsulfanyl-imidazo[1,2-a]pyrazine

6-Methyl-8-methylsulfanyl-imidazo[1,2-a]pyrazine

Product Name
6-Methyl-8-methylsulfanyl-imidazo[1,2-a]pyrazine
CAS No.
1094070-46-8
Chemical Name
6-Methyl-8-methylsulfanyl-imidazo[1,2-a]pyrazine
Synonyms
6-Methyl-8-(Methylthio)iMidazo[1,2-a]pyrazine;Imidazo[1,2-a]pyrazine, 6-methyl-8-(methylthio)-;6-Methyl-8-methylsulfanyl-imidazo[1,2-a]pyrazine
CBNumber
CB12491638
Molecular Formula
C8H9N3S
Formula Weight
179.24
MOL File
1094070-46-8.mol
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6-Methyl-8-methylsulfanyl-imidazo[1,2-a]pyrazine Property

Density 
1.30±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
3.47±0.30(Predicted)
Appearance
Off-white to yellow Solid
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Safety

HS Code 
2933998090
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
M340033
Product name
6-Methyl-8-methylsulfanyl-imidazo[1,2-a]pyrazine
Packaging
50mg
Price
$155
Updated
2021/12/16
Apolloscientific
Product number
OR905621
Product name
6-Methyl-8-methylsulfanyl-imidazo[1,2-a]pyrazine
Packaging
100mg
Price
$254
Updated
2021/12/16
SynQuest Laboratories
Product number
7H66-1-0G
Product name
6-Methyl-8-methylsulfanylimidazo[1,2-a]pyrazine
Purity
98.0%
Packaging
100mg
Price
$301
Updated
2021/12/16
Apolloscientific
Product number
OR905621
Product name
6-Methyl-8-methylsulfanyl-imidazo[1,2-a]pyrazine
Packaging
250mg
Price
$378
Updated
2021/12/16
SynQuest Laboratories
Product number
7H66-1-0G
Product name
6-Methyl-8-methylsulfanylimidazo[1,2-a]pyrazine
Purity
98.0%
Packaging
250mg
Price
$448
Updated
2021/12/16
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6-Methyl-8-methylsulfanyl-imidazo[1,2-a]pyrazine Chemical Properties,Usage,Production

Synthesis

936360-80-4

823-96-1

1094070-46-8

Part C: 6-bromo-3-iodo-8-(methylthio)imidazo[1,2-A]pyrazine (45.6 g), tetrakis(triphenylphosphine)palladium (10.8 g), potassium carbonate (77.4 g), and trimethylcyclotriboroxane (46.9 g) from Part A were suspended in N,N-dimethylformamide (410 mL), and the reaction was heated at 105 °C under nitrogen protection overnight. After completion of the reaction, the reaction was cooled to room temperature, the reaction mixture was diluted with ethyl acetate (1 L), washed sequentially with saturated saline (2×500 mL), the organic phase was dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography to afford 6-methyl-8-(methylthio)-imidazo[1,2-a]pyrazine as a light yellow solid (21.4 g, 64% yield).

References

[1] Patent: WO2009/97233, 2009, A1. Location in patent: Page/Page column 40; 41
[2] Patent: WO2008/156614, 2008, A2. Location in patent: Page/Page column 72; 73

6-Methyl-8-methylsulfanyl-imidazo[1,2-a]pyrazine Preparation Products And Raw materials

Raw materials

Preparation Products

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6-Methyl-8-methylsulfanyl-imidazo[1,2-a]pyrazine Suppliers

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1094070-46-8, 6-Methyl-8-methylsulfanyl-imidazo[1,2-a]pyrazineRelated Search:


  • 6-Methyl-8-methylsulfanyl-imidazo[1,2-a]pyrazine
  • 6-Methyl-8-(Methylthio)iMidazo[1,2-a]pyrazine
  • Imidazo[1,2-a]pyrazine, 6-methyl-8-(methylthio)-
  • 1094070-46-8