51526-03-5 Usage
Description
1,7-Diiodoheptane, also known as heptane-1,7-diyl diiodide, is an organic compound that falls under the category of iodohydrocarbons. These are aliphatic hydrocarbons with one or more iodine atoms. This specific compound features a linear structure with iodine atoms attached at both ends, making it a diiodide. It has a molecular weight of 346.92 g/mol and is known for its strong irritating odor. The properties of 1,7-diiodoheptane indicate its potential use in various fields, such as material science, pharmaceuticals, and organic synthesis. However, it is important to handle this compound with care, as it can cause skin and eye irritation and may be harmful if inhaled or swallowed.
Uses
Used in Material Science:
1,7-Diiodoheptane is used as a chemical intermediate for the synthesis of various materials, contributing to the development of new compounds with unique properties.
Used in Pharmaceutical Industry:
1,7-Diiodoheptane is used as a building block in the synthesis of pharmaceutical compounds, potentially leading to the creation of new drugs with improved therapeutic effects.
Used in Organic Synthesis:
1,7-Diiodoheptane is used as a reagent in organic synthesis processes, enabling the formation of complex molecules and facilitating the development of novel chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 51526-03-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,2 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51526-03:
(7*5)+(6*1)+(5*5)+(4*2)+(3*6)+(2*0)+(1*3)=95
95 % 10 = 5
So 51526-03-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H14I2/c8-6-4-2-1-3-5-7-9/h1-7H2
51526-03-5Relevant articles and documents
Highly Selective Radical Monoreduction of Dihalides Confined to a Dynamic Supramolecular Host
Petroselli, Manuel,Rebek, Julius,Yu, Yang
supporting information, p. 3284 - 3287 (2021/02/05)
Reduction of alkyl dihalide guests (2–5 and 7) with trialkylsilanes (R3SiH) was performed in water-soluble host 1 to investigate the effects of confinement on fast radical reactions (k≥103 m?1 s?1). High selectivity (>95 %) for mono-reduced products was observed for primary and secondary dihalide guests under mild conditions. The results highlight the importance of host–guest complexation rates to modulate the product selectivity in radical reactions.
Synthesis and biological characterization of (Z)-9-heptadecenoic and (Z)-6-methyl-9-heptadecenoic acids: Fatty acids with antibiotic activity produced by Pseudozyma flocculosa
Avis,Boulanger,Belanger
, p. 987 - 1000 (2007/10/03)
Difficulties in isolating and purifying antibiotic fatty acids from culture filtrates of Pseudozyma flocculosa, a biocontrol agent against powdery mildew, have been limiting factors in studying the properties and understanding the mode of action of the biocontrol agent. We report a new protocol for synthesizing (Z)-9-heptadecenoic and for the first time synthesis of (Z)-6-methyl-9-heptadecenoic acids, two antibiotic fatty acids produced by P. flocculosa. This allowed reproducible and quantifiable means of assaying biological activity of the molecules. In these bioassays, both molecules exhibited antifungal activity corresponding to their expected potency. These new developments should facilitate further studies aimed at deciphering the ecological properties of P. flocculosa.
