74744-43-7 Usage
Uses
Used in Organic Synthesis:
(E)-4-Tridecen-6-yne is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for versatile chemical reactions, making it a valuable component in the creation of a wide range of molecules.
Used in Research and Development:
As a research tool, (E)-4-Tridecen-6-yne aids in the study of chemical reactions and the development of new methodologies in organic chemistry. Its distinctive structure provides insights into the behavior of similar compounds and contributes to the advancement of chemical knowledge.
Used in the Development of New Materials:
(E)-4-Tridecen-6-yne is employed in the development of innovative materials due to its potential applications in creating novel compounds with unique properties. Its incorporation into new materials can lead to the discovery of substances with enhanced characteristics for various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, (E)-4-Tridecen-6-yne serves as a starting material for the synthesis of potential drug candidates. Its unique structure may contribute to the development of new therapeutic agents, offering novel treatment options for various medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 74744-43-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,7,4 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 74744-43:
(7*7)+(6*4)+(5*7)+(4*4)+(3*4)+(2*4)+(1*3)=147
147 % 10 = 7
So 74744-43-7 is a valid CAS Registry Number.
74744-43-7Relevant academic research and scientific papers
Cu-catalyzed Fe-driven Csp-Csp and C sp-Csp2 cross-coupling: An access to 1,3-diynes and 1,3-enynes
Ahammed, Sabir,Kundu, Debasish,Ranu, Brindaban C.
, p. 7391 - 7398 (2014/09/17)
An efficient Csp-Csp cross-coupling of alkynyl bromide and pinacol ester of alkynyl boronic acid catalyzed by CuFe 2O4 nanoparticles has been accomplished in dimethyl carbonate to produce unsymmetric 1,3-diynes. This protocol is also extended for the Csp-Csp2 coupling of alkynyl bromide and alkenyl boronic acid to provide conjugated 1,3-enynes. The aliphatic, aromatic, and heteroaromatic alkynes couple with various substituted alkynyl/alkenyl boronates/boronic acids by this procedure to furnish a library of 1,3-diynes and enynes in high yields. The catalyst was easily separated by an external magnet and recycled 10 times.
PHASE-TRANSFER VERSION OF THE WITTIG REACTION AND ITS STEREOCHEMISTRY IN THE ALIPHATIC SERIES
Khusid, A. Kh.,Kovalev, B. G.
, p. 62 - 67 (2007/10/02)
Alkyltriphenylphosphonium salts react with saturated α,β-ethylenic, α,β-acetylenic, and cyclic aliphatic aldehydes when heated with solid potassium carbonate to form the corresponding alkenes with preparative yields.The reaction is cis-stereoselective with saturated aldehydes and cis-stereospecific with unsaturated aldehydes.
