ChemicalBook > CAS DataBase List > 4-METHYL-3,4-DIHYDROQUINOXALIN-2(1H)-ONE

4-METHYL-3,4-DIHYDROQUINOXALIN-2(1H)-ONE

Product Name
4-METHYL-3,4-DIHYDROQUINOXALIN-2(1H)-ONE
CAS No.
67074-63-9
Chemical Name
4-METHYL-3,4-DIHYDROQUINOXALIN-2(1H)-ONE
Synonyms
4-methyl-1,3-dihydroquinoxalin-2-one;4-Methyl-3,4-dihydroquinoxalin-2(1H);3,4-dihydro-4-methyl-2(1H)-Quinoxalinone;4-METHYL-3,4-DIHYDROQUINOXALIN-2(1H)-ONE;2(1H)-Quinoxalinone, 3,4-dihydro-4-methyl-
CBNumber
CB02469067
Molecular Formula
C9H10N2O
Formula Weight
162.19
MOL File
67074-63-9.mol
More
Less

4-METHYL-3,4-DIHYDROQUINOXALIN-2(1H)-ONE Property

storage temp. 
Sealed in dry,Room Temperature
Appearance
White to off-white Solid
More
Less

Hazard and Precautionary Statements (GHS)

More
Less

N-Bromosuccinimide Price

AK Scientific
Product number
0305AC
Product name
4-Methyl-3,4-dihydroquinoxalin-2(1H)-one
Packaging
1g
Price
$451
Updated
2021/12/16
Matrix Scientific
Product number
133252
Product name
4-Methyl-3,4-dihydroquinoxalin-2(1H)-one
Purity
97%
Packaging
5g
Price
$1440
Updated
2021/12/16
Matrix Scientific
Product number
133252
Product name
4-Methyl-3,4-dihydroquinoxalin-2(1H)-one
Purity
97%
Packaging
10g
Price
$2160
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0150722
Product name
4-METHYL-3,4-DIHYDROQUINOXALIN-2(1H)-ONE
Purity
95.00%
Packaging
5G
Price
$2656.5
Updated
2021/12/16
Ambeed
Product number
A164445
Product name
4-Methyl-3,4-dihydroquinoxalin-2(1H)-one
Purity
97%
Packaging
5g
Price
$694
Updated
2021/12/16
More
Less

4-METHYL-3,4-DIHYDROQUINOXALIN-2(1H)-ONE Chemical Properties,Usage,Production

Synthesis

50-00-0

59564-59-9

67074-63-9

The general procedure for the synthesis of 4-methyl-3,4-dihydroquinoxalin-2(1H)-one from formaldehyde and 3,4-dihydroquinoxalin-2(1H)-one was as follows: sodium cyanoborohydride (425 mg, 6.76 mmol) was sequentially added to a methanol (3 mL) solution of 3,4-dihydroquinoxalin-2(1H)-one (500 mg, 3.378 mmol), paraformaldehyde (102 mg) and acetic acid (30 μL). The reaction mixture was stirred at room temperature for 4 hours. Subsequently, another portion of sodium cyanoborohydride (212 mg, 3.37 mmol), paraformaldehyde (51 mg) and concentrated hydrochloric acid (10 μL) was added to the reaction mixture. The reaction mixture was stirred at 50 °C for 5 h and then cooled to room temperature. The pH was adjusted to 8 with base and the solvent was evaporated under reduced pressure. The target product was extracted with ethyl acetate and washed with brine and dried over anhydrous sodium sulfate. After evaporation of the solvent under reduced pressure, 4-methyl-3,4-dihydroquinoxalin-2(1H)-one (537 mg, 98% yield) was obtained as a beige powder.LC-MS ESI m/z 163 [M + H]+.

References

[1] Patent: US2005/261244, 2005, A1. Location in patent: Page/Page column 53
[2] Journal of Medicinal Chemistry, 2013, vol. 56, # 22, p. 9275 - 9295
[3] Patent: CN106317027, 2017, A. Location in patent: Paragraph 0196; 0197; 0198

4-METHYL-3,4-DIHYDROQUINOXALIN-2(1H)-ONE Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

4-METHYL-3,4-DIHYDROQUINOXALIN-2(1H)-ONE Suppliers

A.J Chemicals
Tel
--
Fax
--
Email
sales@ajchem.in
Country
India
ProdList
6100
Advantage
58

67074-63-9, 4-METHYL-3,4-DIHYDROQUINOXALIN-2(1H)-ONERelated Search:


  • 4-METHYL-3,4-DIHYDROQUINOXALIN-2(1H)-ONE
  • 3,4-dihydro-4-methyl-2(1H)-Quinoxalinone
  • 4-Methyl-3,4-dihydroquinoxalin-2(1H)
  • 4-methyl-1,3-dihydroquinoxalin-2-one
  • 2(1H)-Quinoxalinone, 3,4-dihydro-4-methyl-
  • 67074-63-9