53153-67-6 Usage
Uses
Used in Organic Synthesis:
2,3-dimethylnon-2-enenitrile is utilized as a building block in organic synthesis for the creation of various chemical compounds. Its unique structure and reactivity make it a valuable component in the synthesis of complex organic molecules.
Used in Chemical Research:
In the field of chemical research, 2,3-dimethylnon-2-enenitrile serves as a subject for studying the properties and reactions of unsaturated nitriles. This helps in understanding their behavior in different chemical environments and contributes to the advancement of organic chemistry.
Used in Industrial Applications:
Although its use in specific industrial applications is not detailed in the provided materials, 2,3-dimethylnon-2-enenitrile's role as a building block in organic synthesis implies that it may be used in the development of specialty chemicals, pharmaceuticals, or materials in various industries. Its application would be driven by the need for specific chemical properties that it can impart to the final product.
Check Digit Verification of cas no
The CAS Registry Mumber 53153-67-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,1,5 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 53153-67:
(7*5)+(6*3)+(5*1)+(4*5)+(3*3)+(2*6)+(1*7)=106
106 % 10 = 6
So 53153-67-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H19N/c1-4-5-6-7-8-10(2)11(3)9-12/h4-8H2,1-3H3
53153-67-6Relevant academic research and scientific papers
Method for preparing unsaturated nitriles
-
, (2008/06/13)
Alpha, beta-dialkyl conjugated nitriles are disclosed which have interesting perfumistic qualities. These materials have the general structural formula STR1 where R is an aliphatic hydrocarbon radical of about 1 to 15 carbon atoms having no unsaturation in conjugated relationship with either the nitrile unsaturation or the alpha, beta-olefinic unsaturation, and R' and R" are the same or different aliphatic hydrocarbon radicals meeting the description of R, or R' and R", taken together, form a cycloaliphatic radical having about 6 to 15 carbon atoms. They are produced by the reaction of the appropriate aliphatic nitrile and ketone under the influence of a basic catalyst.
