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1-Iododec-1-yne is an organic compound characterized by the presence of an iodine atom and a triple bond in its carbon chain. It is a versatile intermediate in the synthesis of various chemical compounds and materials.

67826-81-7

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67826-81-7 Usage

Uses

Used in Chemical Synthesis:
1-Iododec-1-yne is used as an intermediate in the synthesis of 5,7-Hexadecadiynoic Acid CoA Ester (H283905), which is a derivative of 5,7-Hexadecadiynoic Acid (H283900(M)). This derivative is particularly useful for preparing poly(HDDA)/zinc oxide (ZnO) nanocomposites, a type of material with potential applications in various industries due to its unique properties.
Used in Nanocomposites Industry:
1-Iododec-1-yne is used as a precursor for the development of poly(HDDA)/zinc oxide (ZnO) nanocomposites. These nanocomposites are valued for their enhanced properties, such as improved mechanical strength, thermal stability, and electrical conductivity, making them suitable for applications in electronics, coatings, and other advanced materials.

Check Digit Verification of cas no

The CAS Registry Mumber 67826-81-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,8,2 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67826-81:
(7*6)+(6*7)+(5*8)+(4*2)+(3*6)+(2*8)+(1*1)=167
167 % 10 = 7
So 67826-81-7 is a valid CAS Registry Number.

67826-81-7Relevant academic research and scientific papers

Borane-induced radical reduction of 1-alkenyl- and 1-alkynyl-λ3-iodanes with tetrahydrofuran

Ochiai, Masahito,Tsuchimoto, Yoshimi,Hayashi, Takanori

, p. 5381 - 5384 (2007/10/03)

Exposure of 1-alkenyl(phenyl)- and 1-alkynyl(phenyl)-λ3-iodanes to THF at room temperature in the presence of a catalytic amount of trialkylborane results in smooth reduction to give 1-iodo-1-alkenes and 1-iodo-1-alkynes as major products, respectively. The key step in the reductions probably involves a single-electron transfer from α-tetrahydrofuryl radical to the λ3-iodanes, which generates the labile [9-I-2] iodanyl radicals.

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