215855-49-5 Usage
Alkyne alcohol
The compound is classified as an alkyne alcohol, which means it contains a carbon-carbon triple bond (alkyne) and a hydroxyl (OH) group.
Phenylsulfonyl group
A phenylsulfonyl group (C6H5SO2) is attached to the ninth carbon atom in the compound, giving it additional functional groups and properties.
Potential applications in organic synthesis and biochemistry
The compound can be used as a building block for constructing more complex molecules, making it valuable in the fields of organic synthesis and biochemistry.
Possible biological or pharmacological properties
1-Nonen-7-yn-5-ol, 9-(phenylsulfonyl)may have biological or pharmacological properties that could be studied and utilized in various applications.
Context-dependent uses and effects
The specific uses and effects of the compound will depend on the context in which it is used and the reactions it is involved in, making it important to study its behavior in different scenarios.
Check Digit Verification of cas no
The CAS Registry Mumber 215855-49-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,8,5 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 215855-49:
(8*2)+(7*1)+(6*5)+(5*8)+(4*5)+(3*5)+(2*4)+(1*9)=145
145 % 10 = 5
So 215855-49-5 is a valid CAS Registry Number.
215855-49-5Relevant academic research and scientific papers
General stereoselective synthesis of (E)-exo-alkylidene tetrahydrofurans via base-mediated cyclization of hydroxyl propargylic sulfones
Dai, Wei-Min,Lee, Mavis Yuk Ha
, p. 12497 - 12512 (2007/10/03)
The base-promoted cyclization of a number of phenyl propargylic sulfones possessing a β-hydroxyl group afforded 5-substituted (E)-2- [(benzenesulfonyl)methylene]tetrahydrofurans 3 in >80% yield. The phenyl allenic sulfone, formed by isomerization of the phenyl propargylic sulfone under the basic conditions, is attacked by the internal alkoxide to give an allylic anion which undergoes protonation to form the conjugated exo double bond.
