29509-04-4 Usage
Description
2,4,4-trimethyl-3-oxovaleronitrile, also known as 2-(2,4,4-trimethylpentylidene)malononitrile, is a chemical compound with the molecular formula C9H15NO. It is a colorless liquid that serves as a valuable intermediate in the chemical industry.
Uses
Used in Pharmaceutical Industry:
2,4,4-trimethyl-3-oxovaleronitrile is used as a precursor in the synthesis of various pharmaceuticals. Its role in the production of medicinal compounds is crucial due to its ability to be transformed into a wide range of active ingredients.
Used in Agrochemical Industry:
2,4,4-trimethyl-3-oxovaleronitrile is also utilized as a starting material in the synthesis of agrochemicals, contributing to the development of products that aid in crop protection and enhancement of agricultural yields.
Used in Organic Compounds Synthesis:
2,4,4-trimethyl-3-oxovaleronitrile is used as a building block in the production of various organic compounds, highlighting its versatility in chemical reactions and its importance in creating a diverse array of chemical products.
Used in Chemical Industry:
As a valuable intermediate, 2,4,4-trimethyl-3-oxovaleronitrile is employed in the manufacture of a variety of synthetic materials and products, underlining its significance in the broader chemical sector.
Safety Considerations:
It is important to handle 2,4,4-trimethyl-3-oxovaleronitrile with care and in accordance with proper safety protocols to ensure the safety of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 29509-04-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,5,0 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 29509-04:
(7*2)+(6*9)+(5*5)+(4*0)+(3*9)+(2*0)+(1*4)=124
124 % 10 = 4
So 29509-04-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H13NO/c1-6(5-9)7(10)8(2,3)4/h6H,1-4H3
29509-04-4Relevant articles and documents
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Gardner,D.V.,McGreer,D.E.
, p. 2110 - 2119 (1970)
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Aryl Halides as Convenient Precursors of Electrogenerated Bases. Efficient Syntheses of β-Oxo Nitriles or Esters by Coupling Active-hydrogen Groups with Esters
Barhdadi, Rachid,Gal, Jacques,Heintz, Monique,Troupel, Michel
, p. 50 - 51 (2007/10/02)
In an undivided cell fitted with a sacrificial anode and a nickel cathode on which cadmium had been deposited, the electroreduction of aromatic halides affords a strong base which allows the effective synthesis of β-oxo nitriles or β-oxo esters from the coupling of active-hydrogen compounds with esters.
