1785-53-1 Usage
Uses
Used in Pharmaceutical Synthesis:
2,9-Undecadiyne is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its high reactivity allows for the creation of a wide range of medicinal agents, contributing to the development of new treatments and therapies.
Used in Pesticide Production:
In the agricultural sector, 2,9-Undecadiyne serves as a key intermediate in the production of pesticides. Its role in the synthesis of these chemicals helps in the development of effective pest control solutions.
Used in Organic Chemical Synthesis:
2,9-Undecadiyne is utilized as a versatile intermediate in the synthesis of a broad spectrum of organic chemicals, showcasing its applicability across different chemical industries.
Used in Polymer Production:
2,9-Undecadiyne is used as a precursor in the production of polymers, contributing to the development of new materials with specific properties for various applications.
Used in Modified Hydrocarbon Synthesis:
As a precursor, 2,9-Undecadiyne is involved in the synthesis of modified hydrocarbons, which are important in the creation of advanced materials and compounds with tailored characteristics.
Used in Organic Synthesis Reactions:
Due to its high reactivity, 2,9-undecadiyne is used in various organic synthesis reactions, including cross-coupling reactions and other transformations, enabling the production of complex organic molecules for diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1785-53-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,8 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1785-53:
(6*1)+(5*7)+(4*8)+(3*5)+(2*5)+(1*3)=101
101 % 10 = 1
So 1785-53-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H16/c1-3-5-7-9-11-10-8-6-4-2/h7-11H2,1-2H3
1785-53-1Relevant academic research and scientific papers
Cyclic Diynes by Alkyne Metathesis
Hellbach, Bjoern,Gleiter, Rolf,Rominger, Frank
, p. 2535 - 2541 (2007/10/03)
The preparation of α,ω-diynes with methyl groups at the termini (11a-i) is described. The methylene groups between the alkyne units vary between n = 12 (a) and n = 4 (i). Ring closing metathesis with Mo(CO) 6/CF3C6H4OH yielded the monocyclic alkyne 12a with 11a as starting material, whereas 11b-g yielded the cyclic diynes 13b-g. Detailed structural parameters were obtained for 13b and 13c by X-ray crystallography.
