2-CHLORO-3-METHYL-QUINOXALINE

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Products Intro: Product Name:2-Chloro-3-methylquinoxaline
CAS:32601-86-8
Purity:97%(Min,GC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:2-Chloro-3-methylquinoxaline
CAS:32601-86-8
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-16438
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Products Intro: Product Name:2-Chloro-3-methyl-quinoxaline
CAS:32601-86-8
Purity:0.98 Package:1g;5g;25g;100;500g
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Products Intro: CAS:32601-86-8
Purity:0.99 Package:1kg
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Products Intro: Product Name:2-CHLORO-3-METHYL-QUINOXALINE
CAS:32601-86-8
Purity:99% Package:1KG;1USD

2-CHLORO-3-METHYL-QUINOXALINE manufacturers

2-CHLORO-3-METHYL-QUINOXALINE Basic information
Product Name:2-CHLORO-3-METHYL-QUINOXALINE
Synonyms:TIMTEC-BB SBB010632;Quinoxaline, 2-chloro-3-methyl-;2-Chloro-3-methylquinoxaline ,97%;2-CHLORO-3-METHYL-QUINOXALINE;AKOS BBS-00004537;NSC 38593;2-Chloro-3-methylquinoxaline
CAS:32601-86-8
MF:C9H7ClN2
MW:178.62
EINECS:676-130-2
Product Categories:
Mol File:32601-86-8.mol
2-CHLORO-3-METHYL-QUINOXALINE Structure
2-CHLORO-3-METHYL-QUINOXALINE Chemical Properties
Melting point 91-93℃
Boiling point 259.9±35.0 °C(Predicted)
density 1.292±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka-1.14±0.48(Predicted)
form powder
AppearanceOrange to red Solid
InChI1S/C9H7ClN2/c1-6-9(10)12-8-5-3-2-4-7(8)11-6/h2-5H,1H3
InChIKeyPXDLUYLWPJMGJA-UHFFFAOYSA-N
SMILESCc1nc2ccccc2nc1Cl
Safety Information
Hazard Codes Xi,T
Risk Statements 25-41
Safety Statements 26-39-45
RIDADR UN 2811 6.1 / PGIII
WGK Germany 2
HazardClass IRRITANT
HS Code 29339900
Storage Class6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard ClassificationsAcute Tox. 3 Oral
Eye Dam. 1
MSDS Information
2-CHLORO-3-METHYL-QUINOXALINE Usage And Synthesis
Chemical PropertiesPink solid
Synthesis
3-METHYL-2-QUINOXALINOL

14003-34-0

2-CHLORO-3-METHYL-QUINOXALINE

32601-86-8

GENERAL PROCEDURE: 3-methylquinoxalin-2-ol (28.1 mmol, 5.0 g) was dissolved in phosphorous trichloride (POCl3, 25 mL) at 0°C and the resulting solution was allowed to reflux at 120°C for 5 hours. Upon completion of the reaction, the reaction was quenched with a cooled ammonia solution and extracted with ethyl acetate (EtOAc, 2 x 15 mL). The organic phase was separated and washed with saturated sodium chloride solution, dried over anhydrous magnesium sulfate (MgSO4), filtered, and concentrated in vacuum to give the crude product. The crude product was purified by silica gel fast column chromatography (eluent: petroleum ether/ethyl acetate = 10:1, v/v) to afford 5.0 g 3-methyl-2-chloro-quinoxaline as an off-white solid in 90% yield. Melting point: 86.0-87.0 °C; ESI-MS m/z: 179.4 [M + H]+.

References[1] European Journal of Medicinal Chemistry, 2016, vol. 124, p. 311 - 325
[2] European Journal of Medicinal Chemistry, 2009, vol. 44, # 3, p. 1135 - 1143
[3] Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2001, vol. 40, # 7, p. 565 - 573
[4] E-Journal of Chemistry, 2011, vol. 8, # 2, p. 635 - 642
[5] Journal of Heterocyclic Chemistry, 2007, vol. 44, # 5, p. 1139 - 1143
2-CHLORO-3-METHYL-QUINOXALINE Preparation Products And Raw materials
Raw materialsDichloromethane-->Phosphorus oxitrichloride-->Sodium carbonate-->o-Phenylenediamine-->Pyruvic acid-->3-METHYL-2-QUINOXALINOL
Preparation Products2-AMINO-3-METHYLQUINOXALINE
Tag:2-CHLORO-3-METHYL-QUINOXALINE(32601-86-8) Related Product Information
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