7153-15-3 Usage
Uses
Used in Organic Synthesis:
2-(Cyclohex-1-en-1-yl)butanenitrile is used as a starting material for the synthesis of various organic compounds. Its unique structure and reactivity make it a valuable component in the creation of new molecules with potential applications in different industries.
Used in Chemical Research:
2-(Cyclohex-1-en-1-yl)butanenitrile is used as a research compound to study its properties, reactivity, and potential applications. Understanding its behavior in different chemical reactions can lead to the development of new synthetic pathways and the discovery of novel compounds with specific functions.
Used in Pharmaceutical Industry:
2-(Cyclohex-1-en-1-yl)butanenitrile is used as an intermediate in the synthesis of pharmaceutical compounds. Its unique structure may contribute to the development of new drugs with improved efficacy and reduced side effects.
Used in Agrochemical Industry:
2-(Cyclohex-1-en-1-yl)butanenitrile is used as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its potential reactivity and stability may lead to the development of more effective and environmentally friendly products.
Used in Material Science:
2-(Cyclohex-1-en-1-yl)butanenitrile is used in the development of new materials with specific properties, such as polymers with enhanced mechanical strength or chemical resistance. Its incorporation into these materials can lead to innovative applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 7153-15-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,5 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7153-15:
(6*7)+(5*1)+(4*5)+(3*3)+(2*1)+(1*5)=83
83 % 10 = 3
So 7153-15-3 is a valid CAS Registry Number.
7153-15-3Relevant academic research and scientific papers
2,6-Piperidinediones, I: Synthesis of the Racemates and Enantiomers of 3,3-Disubstituted 2,6-Piperidinediones
Knabe, Joachim,Reischig, Dirk
, p. 353 - 362 (2007/10/02)
The synthesis of the racemates and the enantiomers of the 3,3-disubstituted 2,6-piperidinediones 3a-3g is performed in three ways, depending on the C-3 substituents.The 3-cyclohexylpiperidinedione 3h is obtained as racemic and optically active compound by
