2384-85-2 Usage
Uses
Used in Pharmaceutical Industry:
3-Decyne is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique carbon-carbon triple bond allows for the creation of a wide range of medicinal agents, contributing to the development of new drugs and therapies.
Used in Dye Industry:
In the dye industry, 3-Decyne is utilized as a precursor in the production of various dyes. Its chemical properties make it suitable for the synthesis of dyes with specific color characteristics and stability, enhancing the colorfastness and performance of textiles and other materials.
Used in Plastics Industry:
3-Decyne is employed as a monomer in the production of certain types of plastics. Its ability to form long chains through polymerization contributes to the development of plastics with specific properties, such as flexibility, strength, and durability.
Used as a Solvent:
3-Decyne is used as a solvent in various chemical processes. Its solubility properties allow it to dissolve a wide range of substances, making it a valuable component in the production of various chemical products and formulations.
Used in Synthesis of Other Organic Compounds:
3-Decyne serves as a precursor in the synthesis of other organic compounds. Its carbon-carbon triple bond can be selectively modified or functionalized, enabling the creation of a diverse array of organic molecules with different applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 2384-85-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2384-85:
(6*2)+(5*3)+(4*8)+(3*4)+(2*8)+(1*5)=92
92 % 10 = 2
So 2384-85-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H18/c1-3-5-7-9-10-8-6-4-2/h3-5,7,9-10H2,1-2H3
2384-85-2Relevant articles and documents
Allenes and Acetylenes. 28. On the Mechanism of Reduction of Propargylic Ethers and Acetates with Organocuprates
Sahlberg, Christer,Claesson, Alf
, p. 4120 - 4122 (2007/10/02)
The amounts of substitution and reduction products from the reaction of two types of propargylic methyl ethers and acetates with organocuprates were determined.The methyl ethers give rise to more of the reduction products than the acetates.It is shown that "reduced" allenes are formed by hydrolysis of an organometallic intermediate whereas "reduced" acetyles are formed mainly by another mechanistic pathway.The mechanisms of these reduction reactions are discussed in terms of stabilized, transient Cu(III)-intermediates and concerted β-hydride transfer in the formation of the acetylene.
