56695-54-6 Usage
Description
(6-methylhept-5-en-2-ylidene)propanedinitrile, also known as 5-undecylnitrile, is an organic compound with the chemical formula C13H19N3. It is a cyanide derivative and is classified as an alkylidenemalononitrile. (6-methylhept-5-en-2-ylidene)propanedinitrile is characterized by its versatile reactivity and ability to participate in various chemical reactions, making it a valuable component in the fields of organic synthesis and pharmaceuticals.
Uses
Used in Organic Synthesis:
(6-methylhept-5-en-2-ylidene)propanedinitrile is used as a key intermediate for the synthesis of various organic compounds due to its unique structure and reactivity. Its ability to engage in different chemical reactions allows for the creation of a wide range of products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (6-methylhept-5-en-2-ylidene)propanedinitrile is used as a building block for the development of new drugs. Its unique chemical properties and reactivity contribute to the design and synthesis of novel pharmaceutical compounds.
Used in Agrochemical Production:
(6-methylhept-5-en-2-ylidene)propanedinitrile is utilized as a starting material in the production of agrochemicals, such as pesticides and herbicides. Its chemical properties make it suitable for the development of effective and targeted agrochemical products.
Used in Dye Manufacturing:
(6-methylhept-5-en-2-ylidene)propanedinitrile is also used as a precursor in the manufacturing of dyes. Its reactivity and structural properties enable the production of a variety of dyes with different color characteristics and applications.
Used in Polymer Production:
(6-methylhept-5-en-2-ylidene)propanedinitrile is employed in the synthesis of polymers, contributing to the development of new materials with specific properties and applications.
Potential Applications in Material and Drug Development:
Due to its unique structure and chemical properties, (6-methylhept-5-en-2-ylidene)propanedinitrile may have potential applications in the development of new materials and drugs. Further research and development in this area could lead to innovative products and solutions.
Safety Precautions:
It is important to handle (6-methylhept-5-en-2-ylidene)propanedinitrile with care, as it is toxic and poses health hazards if not handled properly. Appropriate safety measures should be taken during its production, use, and disposal to minimize risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 56695-54-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,9 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56695-54:
(7*5)+(6*6)+(5*6)+(4*9)+(3*5)+(2*5)+(1*4)=166
166 % 10 = 6
So 56695-54-6 is a valid CAS Registry Number.
56695-54-6Relevant articles and documents
Cascade cyclizations of terpenoid polyalkenes triggered by photoelectron transfer-biomimetics with photons
Warzecha,Xing,Demuth,Goddard,Kessler,Kruger
, p. 2065 - 2076 (1995)
Light-induced cyclizations of suitably functionalized polyalkene terpenoids, such as geranyl, all-trans-farnesyl, and all-trans-geranylgeranyl derivatives, via formation of radical cations are proven to be a powerful method for the single-step synthesis of mono- and mostly all-trans-fused polycyclic compounds from readily available precursors. Whereas some of these highly stereo- and chemoselective transformations required the use of micellar media, they can now be conveniently performed in homogeneous solutions upon suitable choice of the electron acceptors and of the functionality pattern of the polyalkene substrates. Moreover, the mode of cyclization, i.e., 6- vs. 5-membered ring formation termination of the cyclization cascades, are steered efficiently by the substituents of the polyalkenes (polyalkenyl acetate vs. α,β-unsaturated ethyl polyalkenoate and polyalkene-1,1-dicarbonitrile). At the same time, the protic solvents used add highly stereoselectivity to the ω-alkene sites of the polyalkenes in anti-Markovnikov sense which strongly suggests that radical cations are intercepted. Interestingly, the transformations achieved here upon photoelectron transfer parallel the biosynthetic paths of non-oxidative terpene cyclizations which are thought to occur purely by protonation of the isoprenoid polyalkenes.
Experimental evidence for a dual site mechanism in Sn-Beta and Sn-MCM-41 catalysts for the Baeyer-Villiger oxidation
Corma, Avelino,Renz, Michael
, p. 1727 - 1736 (2007/10/03)
It is postulated that the catalytic active centre in Sn-Beta and Sn-MCM-41 zeolites for Baeyer-Villiger oxidations involves not only the framework Sn sites but also an associated "basic" oxygen that stabilises the reaction transition state through hydrogen bonding. The presence of these "basic" sites has been studied by cross-polarization MAS NMR H → Sn, and by carrying out the condensation of ketones with malononitrile. The reaction proceeds highly selectively and the reactivity of the substrates corresponds to that of the ketones in the Baeyer-Villiger oxidation with hydrogen peroxide, catalysed with tin-containing molecular sieves.
