1124-79-4 Usage
Uses
Used in Pharmaceutical Industry:
(1Z,6Z)-1,6-Cyclodecadiene is used as a building block for the production of various pharmaceuticals. Its unique structure allows for the synthesis of complex organic molecules that can be utilized in the development of new drugs and medications.
Used in Fragrance Industry:
(1Z,6Z)-1,6-Cyclodecadiene is used as a starting material for the synthesis of various fragrances. Its ability to form complex organic molecules makes it a valuable component in creating unique and diverse scents.
Used in Polymer Industry:
(1Z,6Z)-1,6-Cyclodecadiene is used as a precursor in the production of polymers. Its cyclic structure contributes to the development of polymers with specific properties, such as strength, flexibility, and durability.
Used in Organic Synthesis:
(1Z,6Z)-1,6-Cyclodecadiene is used as a starting material for the synthesis of other cyclic compounds and complex organic molecules. Its versatility in organic chemistry makes it an essential component in the creation of a wide range of chemical products.
Safety Precautions:
Due to its flammable nature, (1Z,6Z)-1,6-Cyclodecadiene should be handled and stored with care in a well-ventilated area to minimize the risk of fire or explosion.
Check Digit Verification of cas no
The CAS Registry Mumber 1124-79-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1124-79:
(6*1)+(5*1)+(4*2)+(3*4)+(2*7)+(1*9)=54
54 % 10 = 4
So 1124-79-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H16/c1-2-4-6-8-10-9-7-5-3-1/h1-2,9-10H,3-8H2/b2-1-,10-9-
1124-79-4Relevant academic research and scientific papers
Simple Designs for the Construction of Complex Trans-Fused Polyether Toxin Frameworks. A Linear Strategy Based on Entropically Favored Oxirane Ring Enlargement in Epoxycycloalkenes Followed by Carbon-Carbon or Carbon-Oxygen Bond-Forming Cyclizations
Alvarez, Eleuterio,Diaz, Maria T.,Perez, Ricardo,Ravelo, Jose L.,Regueiro, Alicia,et al.
, p. 2848 - 2876 (2007/10/02)
A successful design for the construction of trans-fused medium-size cyclic ethers is described.The key features of the synthesis are as follows: (i) intramolecular oxirane ring expansion in cycloalkenes to give bridged oxabicyclic systems and (ii) linear, one- or two-directional synthetic operations which generate external oxocycles in single reaction steps.The general approach involves the intramolecular addition of a stable γ-alkoxy-substituted allylstannane to an aldehyde carbonyl group, and the entire reaction is conducted in a one-pot process which includes the following: (i) vic-diol fragmentation from the bridged oxabicyclic precursor and (ii) Lewis acid-induced cyclization of the resulting aldehyde-allylic tin system.While the present strategy was mostly developed around racemic models, the potential for adoption of enantioselective features is immediate.The versatility, scope, limitations, and potential applications of the present technology are discussed in detail.
