174063-93-5 Usage
Uses
Used in Organic Chemistry:
5,7-Eicosadiyn-1-ol is used as a reactant for the synthesis of various functionalized molecules in the field of organic chemistry. Its versatility in undergoing different chemical reactions makes it a valuable component in creating new compounds.
Used in Material Development:
5,7-Eicosadiyn-1-ol is used as a potential component in the development of novel materials. Its unique structure and reactivity contribute to the exploration of new material properties and applications.
Used in Pharmaceutical Research:
5,7-Eicosadiyn-1-ol is used as a starting material in pharmaceutical research for the development of new drugs. Its chemical properties allow for the creation of diverse molecular structures with potential therapeutic effects.
Used in Biomedical Applications:
5,7-Eicosadiyn-1-ol is used in biomedical applications for the development of new compounds with potential use in medical treatments and diagnostics. Its reactivity and structural features make it a promising candidate for further exploration in this field.
Check Digit Verification of cas no
The CAS Registry Mumber 174063-93-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,0,6 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 174063-93:
(8*1)+(7*7)+(6*4)+(5*0)+(4*6)+(3*3)+(2*9)+(1*3)=135
135 % 10 = 5
So 174063-93-5 is a valid CAS Registry Number.
InChI:InChI=1/C20H34O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21/h21H,2-12,17-20H2,1H3
174063-93-5Relevant academic research and scientific papers
Topochemical polymerization of phenylacetylene macrocycles: A new strategy for the preparation of organic nanorods
Rondeau-Gagné, Simon,Néabo, Jules Roméo,Desroches, Maude,Larouche, Jérémie,Brisson, Josée,Morin, Jean-Francìois
, p. 110 - 113 (2013/02/23)
Soluble organic nanorods were prepared from phenylacetylene macrocycles using the topochemical polymerization of butadiyne moieties placed both inside and outside the macrocycles' skeletons. Macrocycles containing amide groups were self-assembled in a columnar fashion through the formation of an organogel in ethyl acetate. Upon irradiation with UV light, the Raman signals associated with butadiyne units completely vanished, indicating the creation of covalently linked nanorods.
