6088-91-1 Usage
1-Iodobuta-1,3-diyne Properties
A linear alkyne with four carbon atoms, three hydrogen atoms, and one iodine atom.
Terminal triple bond
A triple bond at the first carbon atom, contributing to its reactivity and versatility in organic chemistry.
Iodine atom attached to the first carbon
The presence of the iodine atom enhances the compound's reactivity and utility in various chemical reactions.
Versatile building block
1-Iodobuta-1,3-diyne is a valuable intermediate in organic synthesis due to its ability to undergo a wide range of reactions.
Useful reagent
It is commonly used in the synthesis of various functionalized molecules, including pharmaceuticals, agrochemicals, and other fine chemicals.
Synthetic organic reactions
1-Iodobuta-1,3-diyne is widely used in the synthesis of complex organic molecules, contributing to the development of new drugs, agrochemicals, and specialty chemicals.
New materials development
The compound's unique structural properties and reactivity make it a valuable tool in the development of advanced materials.
Natural product synthesis
1-Iodobuta-1,3-diyne can be employed in the synthesis of complex natural products, aiding in the discovery of new bioactive compounds and potential therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 6088-91-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,8 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6088-91:
(6*6)+(5*0)+(4*8)+(3*8)+(2*9)+(1*1)=111
111 % 10 = 1
So 6088-91-1 is a valid CAS Registry Number.
6088-91-1Relevant articles and documents
Photochemistry of Hydrogen Iodide-Acetylene Complexes in Solid Krypton
Abrash, Samuel A.,Pimentel, George C.
, p. 5828 - 5834 (2007/10/02)
Hydrogen iodide-acetylene complexes in a krypton matrix at 12 K have been photolyzed with a medium-pressure mercury lamp.Infrared spectra identify products vinyl iodide and iodoacetylene.When HI*C2D2 complexes are photolyzed, isotopic exchange occurs to produce DI*HCCD.Growth curves show that all three are primary products.As well, the growth curves show secondary photolysis of vinyl iodide and DI*HCCD, but apparently production and secondary photolysis of vinyl iodide only catalyze isotopic exchange.The growth curves obtained for HCCI and DCCI from HI*C2D2 differ from those obtained from DI*C2H2.Short photolysis of HI*C2D2 gives almost exclusively HD*DCCI whereas short photolysis of DI*C2H2 gives HD*HCCI.Thus the hydrogen atom in the hydrogen iodode always ends up in the molecular hydrogen product.We conclude that photolytic production of iodoacetylene involves hydrogen atom abstraction from acetylene by the energetic hydrogen iodide.
