ChemicalBook > CAS DataBase List > 4-Chloro-6-methoxy-2-methylquinazoline

4-Chloro-6-methoxy-2-methylquinazoline

Product Name
4-Chloro-6-methoxy-2-methylquinazoline
CAS No.
60395-90-6
Chemical Name
4-Chloro-6-methoxy-2-methylquinazoline
Synonyms
4-Chloro-6-methoxy-2-methylquinazoline;Quinazoline, 4-chloro-6-methoxy-2-methyl-
CBNumber
CB93065021
Molecular Formula
C10H9ClN2O
Formula Weight
208.64
MOL File
60395-90-6.mol
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4-Chloro-6-methoxy-2-methylquinazoline Property

storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
Appearance
Light yellow to khaki Solid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
C377170
Product name
4-chloro-6-methoxy-2-methylquinazoline
Packaging
2.5mg
Price
$45
Updated
2021/12/16
TRC
Product number
C377170
Product name
4-chloro-6-methoxy-2-methylquinazoline
Packaging
25mg
Price
$265
Updated
2021/12/16
AK Scientific
Product number
4776CT
Product name
4-Chloro-6-methoxy-2-methylquinazoline
Packaging
1g
Price
$448
Updated
2021/12/16
Chemenu
Product number
CM123372
Product name
4-chloro-6-methoxy-2-methylquinazoline
Purity
97%
Packaging
5g
Price
$813
Updated
2021/12/16
Ambeed
Product number
A444705
Product name
4-Chloro-6-methoxy-2-methylquinazoline
Purity
97%
Packaging
5g
Price
$853
Updated
2021/12/16
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4-Chloro-6-methoxy-2-methylquinazoline Chemical Properties,Usage,Production

Synthesis

51413-71-9

60395-90-6

6-Methoxy-2-methylquinazolin-4-ol (233 mg, 1.23 mmol) was used as starting material and suspended in phosphoryl chloride (POCl3, 10 mL, 108 mmol). The reaction mixture was stirred under reflux conditions for 2.5 days and a gradual transformation of the suspension into a reddish brown solution was observed. Upon completion of the reaction, the mixture was cooled to room temperature and the excess phosphoryl chloride was subsequently removed by evaporation under reduced pressure. The residue was partitioned between 5% aqueous sodium bicarbonate solution (NaHCO3, 100 mL) and ethyl acetate (100 mL) for extraction. The organic layer was washed sequentially with 5% aqueous sodium bicarbonate solution (100 mL) and pure water (100 mL). The washed organic layer was dried with anhydrous sodium sulfate (Na2SO4) and subsequently concentrated under reduced pressure. The crude product was purified by silica gel column chromatography using cyclohexane/ethyl acetate as eluent. The final target product, 4-chloro-6-methoxy-2-methylquinazoline, was obtained as a white solid (142 mg, 0.681 mmol) in 56% yield. The product was characterized by 1H NMR (400 MHz, DMSO-d6) and UPLC-MS (ESI): 1H NMR δ 7.92 (d, J = 9.1 Hz, 1H), 7.70 (dd, J = 9.1, 2.8 Hz, 1H), 7.42 (d, J = 2.8 Hz, 1H), 3.96 (s, 3H), 2.71 (s, 3H); UPLC-MS (ESI) RT 3.88 min, m/z 209 [M + H]+ (purity >95%).

References

[1] European Journal of Medicinal Chemistry, 2017, vol. 125, p. 890 - 901

4-Chloro-6-methoxy-2-methylquinazoline Preparation Products And Raw materials

Raw materials

Preparation Products

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4-Chloro-6-methoxy-2-methylquinazoline Suppliers

Chiba Pharmaceutical Science and technology Co, Ltd.
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60395-90-6, 4-Chloro-6-methoxy-2-methylquinazolineRelated Search:


  • 4-Chloro-6-methoxy-2-methylquinazoline
  • Quinazoline, 4-chloro-6-methoxy-2-methyl-
  • 60395-90-6