6-CHLORO-7-METHYLPURINE

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Company Name: Capot Chemical Co.,Ltd.
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Products Intro: Product Name:6-Chloro-7-methylpurine
CAS:5440-17-5
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:6-CHLORO-7-METHYLPURINE
CAS:5440-17-5
Purity:95%-99.99% Package:1KG;1USD
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Products Intro: Product Name:6-CHLORO-7-METHYLPURINE
CAS:5440-17-5
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CAS:5440-17-5
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Company Name: Aladdin Scientific
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Products Intro: Product Name:6-Chloro-7-methylpurine
CAS:5440-17-5
Purity:95% Package:$52.9/50mg;$117.9/250mg;$279.9/1g;Bulk package Remarks:95%

6-CHLORO-7-METHYLPURINE manufacturers

6-CHLORO-7-METHYLPURINE Basic information
Product Name:6-CHLORO-7-METHYLPURINE
Synonyms:6-CHLORO-7-METHYLPURINE;7-METHYL-6-CHLOROPURINE;NSC 15192;6-Chloro-7-methyl-7H-purine;7H-Purine, 6-chloro-7-methyl-
CAS:5440-17-5
MF:C6H5ClN4
MW:168.58
EINECS:
Product Categories:Bases & Related Reagents;Nucleotides
Mol File:5440-17-5.mol
6-CHLORO-7-METHYLPURINE Structure
6-CHLORO-7-METHYLPURINE Chemical Properties
Melting point 175-185°C
Boiling point 321.7±45.0 °C(Predicted)
density 1.59±0.1 g/cm3(Predicted)
storage temp. Inert atmosphere,2-8°C
solubility Chloroform (Slightly), Dichloromethane (Slightly), DMSO (Slightly)
form Solid
pka0.65±0.30(Predicted)
color Light Green to Grey-Blue
CAS DataBase Reference5440-17-5
Safety Information
HS Code 2933998090
MSDS Information
6-CHLORO-7-METHYLPURINE Usage And Synthesis
Chemical PropertiesLight Green Solid
Uses6-CHLORO-7-METHYLPURINE is a useful synthetic intermediate.
Synthesis
6-Chloropurine

87-42-3

Iodomethane

74-88-4

6-CHLORO-7-METHYLPURINE

5440-17-5

To a 1L three-necked round-bottomed flask was added 6-chloro-9H-purine (15.4 g, 0.1 mol, 1 eq.) and tetrahydrofuran (155 mL) at 0 °C and protected by nitrogen in an inert atmosphere. Methylmagnesium chloride (MeMgCl, 36.6 mL, 1.0 M THF solution, 1.1 eq.) was added dropwise with stirring. The reaction mixture was continued to be stirred at 0 °C for 30 min. Subsequently, iodomethane (42.6 g, 3 eq.) was added slowly and dropwise with stirring. The resulting reaction solution was transferred to a 50 °C oil bath and the reaction was stirred for 5 hours. Upon completion of the reaction, the reaction was quenched by addition of 50 mL of aqueous ammonium chloride (NH4Cl) and extracted with dichloromethane (3 x 50 mL). The organic layers were combined and washed with brine (2 x 50 mL) and subsequently concentrated under vacuum. The crude product was recrystallized by dichloromethane/petroleum ether (1:10) to afford 6-chloro-7-methylpurine as a light green solid (7 g, 42% yield).

References[1] Organic Letters, 2016, vol. 18, # 1, p. 16 - 19
[2] Patent: WO2018/96159, 2018, A1. Location in patent: Paragraph 0169-0172
Tag:6-CHLORO-7-METHYLPURINE(5440-17-5) Related Product Information
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