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

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
Molecular Weight:
179.24
MDL Number:
MFCD17215754
MOL File:
1094070-46-8.mol
MSDS File:
SDS
Last updated:2025-07-24 18:13:41

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

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

SAFETY

Risk and Safety Statements

HS Code  2933998090

6-Methyl-8-methylsulfanyl-imidazo[1,2-a]pyrazine price More Price(19)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC M340033 6-Methyl-8-methylsulfanyl-imidazo[1,2-a]pyrazine 1094070-46-8 50mg $155 2021-12-16 Buy
Apolloscientific OR905621 6-Methyl-8-methylsulfanyl-imidazo[1,2-a]pyrazine 1094070-46-8 100mg $254 2021-12-16 Buy
SynQuest Laboratories 7H66-1-0G 6-Methyl-8-methylsulfanylimidazo[1,2-a]pyrazine 98.0% 1094070-46-8 100mg $301 2021-12-16 Buy
Apolloscientific OR905621 6-Methyl-8-methylsulfanyl-imidazo[1,2-a]pyrazine 1094070-46-8 250mg $378 2021-12-16 Buy
SynQuest Laboratories 7H66-1-0G 6-Methyl-8-methylsulfanylimidazo[1,2-a]pyrazine 98.0% 1094070-46-8 250mg $448 2021-12-16 Buy
Product number Packaging Price Buy
M340033 50mg $155 Buy
OR905621 100mg $254 Buy
7H66-1-0G 100mg $301 Buy
OR905621 250mg $378 Buy
7H66-1-0G 250mg $448 Buy

6-Methyl-8-methylsulfanyl-imidazo[1,2-a]pyrazine Chemical Properties,Uses,Production

Synthesis

6-BroMo-3-iodo-8-Methylsulfanyl-iMidazo[1,2-a]pyrazine

936360-80-4

Trimethylboroxine

823-96-1

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

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

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]pyrazine)Related 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