1573-66-6 Usage
Uses
Used in Organic Synthesis:
1-Hexen-5-yn-3-ol is used as a key intermediate in the synthesis of various organic compounds for research and development purposes. Its unique structure with a double bond and a triple bond allows for versatile chemical reactions, making it a valuable component in the creation of new molecules.
Used in Chemical Research:
In the field of chemical research, 1-Hexen-5-yn-3-ol serves as a model compound for studying the reactivity and properties of alcohols with unsaturated carbon chains. It aids in understanding the behavior of such compounds under different conditions, contributing to the advancement of chemical knowledge.
Used in Pharmaceutical Industry:
1-Hexen-5-yn-3-ol is used as a starting material or building block in the development of pharmaceutical compounds. Its unique structure may contribute to the creation of novel drugs with specific therapeutic properties, making it a promising candidate for medicinal chemistry.
Used in Fragrance Industry:
Due to its distinct odor, 1-Hexen-5-yn-3-ol is utilized in the fragrance industry as a component in the formulation of various scents. Its ability to impart unique aroma characteristics makes it valuable in the creation of perfumes, colognes, and other scented products.
Check Digit Verification of cas no
The CAS Registry Mumber 1573-66-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1573-66:
(6*1)+(5*5)+(4*7)+(3*3)+(2*6)+(1*6)=86
86 % 10 = 6
So 1573-66-6 is a valid CAS Registry Number.
1573-66-6Relevant academic research and scientific papers
Nonracemic homopropargylic alcohols via asymmetric allenylboration with the robust and versatile 10-TMS-9-borabicyclo[3.3.2]decanes
Lai, Chunqiu,Soderquist, John A.
, p. 799 - 802 (2007/10/03)
(Chemical Equation Presented) The asymmetric allenylboration of representative aldehydes with the stable, storable 1 is reported. Easily and efficiently prepared in either enantiomeric form from the air-stable crystalline 4 through simple Grignard procedures, 1 gives 6 cleanly. The latter is easily isolated in high yield and ee with predictable stereochemistry. The procedure also regenerates 4 for its direct conversion back to 1 and facilitates the efficient recovery of the pseudoephedrine. The net process is the synthetic equivalent of the asymmetric addition of allenylmagnesium bromide to aldehydes.
