24471-54-3 Usage
Uses
Used in Organic Synthesis:
1-(Iodomethyl)-naphthalene is used as a reactant in organic synthesis for the preparation of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, making it a versatile building block in the synthesis of complex organic molecules.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 1-(iodomethyl)-naphthalene serves as a precursor for the synthesis of various pharmaceuticals. Its reactivity and structural features enable the development of new drugs with potential therapeutic applications.
Used in Agrochemical Production:
1-(Iodomethyl)-naphthalene is also utilized as a starting material in the synthesis of agrochemicals. Its properties make it suitable for the development of compounds used in agriculture to protect crops and enhance yields.
Used in Specialty Chemicals:
1-(IODOMETHYL)-NAPHTHALENE has been employed in the preparation of dyes, optical brighteners, and other specialty chemicals. Its unique chemical properties contribute to the development of innovative products with specific applications in various industries.
Safety Precautions:
It is crucial to handle 1-(iodomethyl)-naphthalene with care due to its potential hazards as a toxic and harmful substance. Proper safety measures should be taken to minimize exposure and ensure the well-being of individuals working with this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 24471-54-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,7 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 24471-54:
(7*2)+(6*4)+(5*4)+(4*7)+(3*1)+(2*5)+(1*4)=103
103 % 10 = 3
So 24471-54-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H9I/c12-8-10-6-3-5-9-4-1-2-7-11(9)10/h1-7H,8H2
24471-54-3Relevant academic research and scientific papers
Synthesis of 1-naphthaldehydes via the cascade reactions of 1-phenylpent-4-yn-2-ols promoted by iodine monochloride
Li, Bin,Shen, Nana,Fan, Xuesen,Zhang, Xinying
, p. 1843 - 1846 (2016/04/19)
A novel and convenient synthesis of 1-naphthaldehydes through iodine monochloride promoted cascade reactions of 1-phenylpent-4-yn-2-ols is presented. Compared with literature procedures, this new method has advantages such as simple operation procedure, mild reaction conditions, good efficiency, and excellent regio-selectivity.
Reduction of benzylic alcohols and α-hydroxycarbonyl compounds by hydriodic acid in a biphasic reaction medium
Dobmeier, Michael,Herrmann, Josef M.,Lenoir, Dieter,Koenig, Burkhard
supporting information; experimental part, p. 330 - 336 (2012/05/20)
The synthetic protocol for the reduction of alcohols to hydrocarbons by using hydriodic acid, first described by Kiliani more than 140 years ago, was improved to be more applicable to organic synthesis. Instead of a strongly acidic, aqueous solution, a biphasic toluene-water reaction medium was used, which allowed the conversion of primary, secondary and tertiary benzylic alcohols, in good yields and short reaction times, into the corresponding hydrocarbons. Red phosphorous was used as the stoichiometric reducing agent. Keto, ester, amide or ether groups are tolerated, and catalytic amounts of hydriodic acid (0.2 equiv) in the presence of 0.6 equiv phosphorous are sufficient to achieve conversion.
