4904-61-4 Usage
Description
Cyclododeca-1,5,9-triene is a colorless liquid that is toxic by skin absorption and ingestion. It is also irritating to the skin and eyes. Cyclododeca-1,5,9-triene is primarily used as a precursor in the synthesis of various chemicals.
Uses
Used in Chemical Synthesis:
Cyclododeca-1,5,9-triene is used as a chemical intermediate for the production of other chemicals. Its unique structure and reactivity make it a valuable building block in the synthesis of a wide range of compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Cyclododeca-1,5,9-triene is used as a starting material for the synthesis of various pharmaceutical compounds. Its versatility in chemical reactions allows for the creation of diverse drug candidates with potential therapeutic applications.
Used in Polymer Industry:
Cyclododeca-1,5,9-triene is also utilized in the polymer industry as a monomer for the production of specialty polymers. These polymers can have unique properties, such as enhanced strength, flexibility, or chemical resistance, making them suitable for specific applications in various industries.
Used in Agrochemical Industry:
In the agrochemical industry, Cyclododeca-1,5,9-triene is used as a precursor for the synthesis of various agrochemicals, such as pesticides and herbicides. Its role in creating these compounds contributes to the development of more effective and targeted agricultural products.
Overall, Cyclododeca-1,5,9-triene is a versatile compound with a wide range of applications across different industries, primarily due to its use as a chemical intermediate and its potential for creating various chemical products.
Reactivity Profile
Cyclododeca-1,5,9-triene may react vigorously with strong oxidizing agents. May react exothermically with reducing agents to release hydrogen gas. In the presence of various catalysts (such as acids) or initiators, may undergo exothermic addition polymerization reactions.
Health Hazard
Exposure can cause irritation and burns of eyes, nose and throat.
Flammability and Explosibility
Notclassified
Check Digit Verification of cas no
The CAS Registry Mumber 4904-61-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,0 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4904-61:
(6*4)+(5*9)+(4*0)+(3*4)+(2*6)+(1*1)=94
94 % 10 = 4
So 4904-61-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H18/c1-2-4-6-8-10-12-11-9-7-5-3-1/h1-2,7-10H,3-6,11-12H2/b2-1-,9-7-,10-8-
4904-61-4Relevant articles and documents
PROCESS FOR PREPARING CYCLODODECATRIENE
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Page/Page column 3, (2008/06/13)
Preparation of cyclododecatriene in a continuous or discontinuous process by trimerization of butadiene in the presence of a catalyst system and a solvent, the crude cyclododecatriene obtained being able to be isolated by means of distillation. The cyclooctadiene formed as by-product can likewise be isolated from the crude product.
Titanium-catalyzed [4+2] and [6+2] cycloadditions of 1,4-bis(trimethylsilyl)buta-1,3-diyne
Kaagman, Jan-Willem F.,Rep, Marco,Horacek, Michal,Sedmera, Petr,Cejka, Jiri,Varga, Vojtech,Mach, Karel
, p. 1722 - 1728 (2007/10/03)
The (C2H5)2AlCl/TiCl4 catalyst induces the [4+2] cycloaddition of butadiene or the [6+2] cycloaddition of 1,3,5-cycloheptatriene (CHT) to individual acetylenic moieties of 1,4-bis(trimethylsilyl)buta-1,3-diyne (BSD). Heating of the 2:1 butadiene adduct, bis(2-trimethylsilylcyclohexa-1,4-dien-1-yl), to 250°C yields 2,2′-bis(trimethylsilyl)biphenyl. The 1:1 adduct of BSD with CHT, 7-trimethylsilyl-8-trimethylsilylethynylbicyclo[4.2.1]nona-2,4-diene, is obtained as virtually the only product if the initial molar ratio CHT:BD equal to 1.86 is used.
OLIGOMERIZATION OF BUTADIENE IN THE PRESENCE OF METAL COMPOUNDS IMMOBILIZED ON POLYMERIC CARRIERS. COMMUNICATION 1. IRON COMPLEXES IMMOBILIZED IN THE BULK OF A POLYMER GEL IN THE REACTION OF LINEAR DIMERIZATION OF BUTADIENE
Potapov, G. P.,Punegov, V. V.,Dzhemilev, U. M.
, p. 1342 - 1345 (2007/10/02)
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