Welcome to LookChem.com Sign In|Join Free

CAS

  • or

6630-11-1

Post Buying Request

6630-11-1 Suppliers

Recommended suppliersmore

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

6630-11-1 Usage

Description

Bis(6-methyl-2-pyridyl) diketone, also known as MMDK, is a chemical compound with the molecular formula C16H14N2O2. It is a bidentate ligand commonly used in coordination chemistry and organometallic chemistry. MMDK is known for its ability to form stable complexes with metal ions, and it is often utilized in the synthesis of metal-organic frameworks and coordination polymers. Bis(6-methyl-2-pyridyl) diketone is widely studied for its potential applications in catalysis, materials science, and medicinal chemistry. Bis(6-methyl-2-pyridyl) diketone is a versatile and valuable chemical reagent with a wide range of potential uses in various chemical and biological processes.

Uses

Used in Coordination Chemistry:
Bis(6-methyl-2-pyridyl) diketone is used as a bidentate ligand for forming stable complexes with metal ions. Its ability to chelate metal ions makes it a valuable reagent in the synthesis of metal-organic frameworks and coordination polymers.
Used in Organometallic Chemistry:
MMDK is used as a ligand in organometallic chemistry to stabilize metal complexes, which can be employed in various catalytic processes.
Used in Catalysis:
Bis(6-methyl-2-pyridyl) diketone is used as a catalyst or catalyst precursor in various chemical reactions, owing to its ability to form stable complexes with metal ions and its potential to modulate the reactivity and selectivity of the catalysts.
Used in Materials Science:
MMDK is used in the development of new materials, such as metal-organic frameworks and coordination polymers, which have potential applications in gas storage, separation, and sensing.
Used in Medicinal Chemistry:
Bis(6-methyl-2-pyridyl) diketone is used as a building block or a ligand in the design and synthesis of new pharmaceutical compounds, taking advantage of its ability to form stable complexes with metal ions and its potential to modulate biological activity.

Check Digit Verification of cas no

The CAS Registry Mumber 6630-11-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6630-11:
(6*6)+(5*6)+(4*3)+(3*0)+(2*1)+(1*1)=81
81 % 10 = 1
So 6630-11-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H12N2O2/c1-9-5-3-7-11(15-9)13(17)14(18)12-8-4-6-10(2)16-12/h3-8H,1-2H3

6630-11-1Relevant articles and documents

2,2′-Pyridoin derivatives protect HL-60 cells against oxidative stress

Hatanaka, Masashi,Nishizawa, Chiho,Kakinoki, Tomohiro,Takahashi, Kyoko,Nakamura, Shigeo,Mashino, Tadahiko

, p. 5290 - 5293 (2008)

Focusing on 2,2′-pyridoin (1, 1,2-di(2-pyridyl)-1,2-ethenediol) and its synthetic derivatives as the lead compound of the potent antioxidative enediol, their protective effect against oxidative stress was evaluated on the HL-60 cell system. 2,2′-Pyridoins showed no remarkable cytotoxic effect on HL-60 cells. The derivatives 1, 2, 3, 5, and 6 inhibited H2O2-induced cell death and intracellular oxidative stress more significantly than ascorbic acid. Since 2,2′-pyridoins are oxidized to the diketones, 2,2′-pyridils, in a protic solvent, the antioxidant activity of 2,2′-pyridils was also investigated. 2,2′-Pyridils showed antioxidant activity in the cell; however, the activity was lower than that of 2,2′-pyridoins. These results suggested that 2,2′-pyrdoin derivatives can be good cytoprotective agents against oxidative stress.

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

What can I do for you?
Get Best Price

Get Best Price for 6630-11-1