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2,2,6,6-Tetramethylheptane-3,5-dione CAS NO: 1118-71-4

2,2,6,6-Tetramethylheptane-3,5-dione CAS NO: 1118-71-4

Name: 2,2,6,6-Tetramethylheptane-3,5-dione
CAS NO: 1118-71-4
Purity: 98% min
MF: C11H20O2
MW:184.28
BP:202.8¡À0.0 ¡ãC at 760 mmHg
Density:0.9¡À0.1 g/cm3

Description of 2,2,6,6-Tetramethyl-3,5-heptanedione (TMTD) CAS NO: 1118-71-4

 

Name: 2,2,6,6-Tetramethylheptane-3,5-dione   

CAS NO: 1118-71-4

Purity: 99% min

MF: C11H20O2

MW:184.28

BP:202.8±0.0 °C at 760 mmHg

Density:0.9±0.1 g/cm3

MP: >400 °C (decomp)

EINECS:214-268-3

Appearance: Colorless to light yellow Liquid(under the 15-20°C,it ill be crystallization)

Package: 25g, 100g, 500g, bulk package

Application:Pharmaceutical Intermediates

 

Other name:

2,2,6,6-Tetramethyl-3,5-Heptanedione;

3,5-Heptanedione, 2,2,6,6-tetramethyl-;

2,2,6,6-Tetramethyl-3,5-heptanedione dipivaloylmethane;

Dipivaloylmethane;

4

Application of 2,2,6,6-Tetramethyl-3,5-heptanedione (TMTD) CAS NO: 1118-71-4

 

Biology: The compound's metal complexes are investigated for their biological activity, including potential antimicrobial and anticancer properties.

Medicine: Research is ongoing into the use of dipivaloylmethane derivatives in drug development, particularly for their ability to chelate metal ions and modulate biological pathways.

Industry: In industrial applications, dipivaloylmethane is used as a precursor for the synthesis of various fine chemicals and as a stabilizer in polymer production.


Dipivaloylmethane has a wide range of uses and can be used as catalysts for a variety of organic synthesis reactions. More importantly, Dipivaloylmethane metal complexes can be widely used as MOCVD precursors and further prepared as semiconductor materials such as noble metal thin films .

 

 

2,2,6,6-Tetramethyl-3,5-heptanedione (TMTD) CAS NO: 1118-71-4 is a picolinic acid analog that binds to receptor molecules. It has been shown to be a potent inhibitor of methanol dehydrogenase with an IC50 of 5 μM. TMTD also has the ability to form stable complexes with zirconium oxide and other metals. These complexes are formed by intramolecular hydrogen bonds and can be used in organometallic synthesis. Structural analysis of these complexes have revealed that the metal is coordinated by two nitrogen atoms and one hydroxyl group from the ligand.

 

 

 

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