Welcome to LookChem.com Sign In|Join Free
  • or
(4-Methoxy-phenyl)-(1-methyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-methanone is a complex organic compound characterized by its unique molecular structure. It features a 4-methoxy-phenyl group, which is a phenyl ring with a methoxy substituent at the 4th position, and a 1-methyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl group, which is a pyrazolo[3,4-d]pyrimidine ring system with a methyl group at the 1st position and a carbonyl group attached to the 4th position. (4-methoxy-phenyl)-(1-methyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-methanone is a derivative of pyrazolo[3,4-d]pyrimidines, which are known for their potential applications in medicinal chemistry, particularly as inhibitors of various enzymes and receptors. The specific arrangement of functional groups in (4-methoxy-phenyl)-(1-methyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-methanone may confer distinct biological activities, making it a subject of interest for further research and development in the field of drug discovery.

59564-09-9

Post Buying Request

59564-09-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

59564-09-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59564-09-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,6 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 59564-09:
(7*5)+(6*9)+(5*5)+(4*6)+(3*4)+(2*0)+(1*9)=159
159 % 10 = 9
So 59564-09-9 is a valid CAS Registry Number.

59564-09-9Relevant academic research and scientific papers

Catalytic action of azolium salts. IV. Preparations of 4-aroylquinazolines and 4-aroyl-1H-pyrazolo[3,4-d]pyrimidines by catalytic action of 1,3-dimethylimidazolium iodide

Miyashita,Matsuda,Suzuki,Iwamoto,Higashino

, p. 2017 - 2022 (2007/10/02)

The ability of 1,3-dimethylimidazolium iodide (1) to catalyze the aroylation of the chloroheteroarenes 4-8 with arenecarbaldehydes 3 as sources of the aroyl groups was examined in order to develop a preparative method of aroylheteroarenes. In the presence

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 59564-09-9