Welcome to LookChem.com Sign In|Join Free
  • or
6-Fluorobenzo[cd]indol-2(1H)-one is a chemical compound with the molecular formula C12H6FNO. It is a fluorinated derivative of the benzoindole骨架, which is a fused ring system consisting of a benzene ring and an indole ring. 6-fluorobenzo[cd]indol-2(1H)-one is characterized by the presence of a fluorine atom at the 6-position of the benzene ring. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique electronic properties and potential for further functionalization. The compound is typically synthesized through various chemical reactions, such as the fluorination of the corresponding non-fluorinated benzoindole, and can be used as a building block for more complex molecules. Its properties, such as reactivity and stability, make it a valuable component in the development of new drugs and other chemical products.

2059-29-2

Post Buying Request

2059-29-2 Suppliers

Recommended suppliers

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

2059-29-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2059-29-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,5 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2059-29:
(6*2)+(5*0)+(4*5)+(3*9)+(2*2)+(1*9)=72
72 % 10 = 2
So 2059-29-2 is a valid CAS Registry Number.

2059-29-2Downstream Products

2059-29-2Relevant academic research and scientific papers

Cobalt-Catalyzed Direct Carbonylative Synthesis of Free (NH)-Benzo[ cd]indol-2(1 H)-ones from Naphthylamides

Ying, Jun,Fu, Lu-Yang,Zhong, Guoqiang,Wu, Xiao-Feng

, p. 5694 - 5698 (2019)

A cobalt-catalyzed C-H carbonylation of naphthylamides for the synthesis of benzo[cd]indol-2(1H)-one scaffolds has been developed. The reaction employs a traceless directing group and uses benzene-1,3,5-triyl triormate as the CO source, affording various free (NH)-benzo[cd]indol-2(1H)-ones in moderate to high yields (up to 88%). Using this protocol, the total synthesis of BET bromodomain inhibitors A and B was accomplished as well.

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 2059-29-2