17025-47-7 Usage
Uses
Used in Plastics Industry:
Phenyl tribromomethyl sulfone is used as a flame retardant for enhancing the fire resistance of various plastic products. Its ability to inhibit the spread of fire and high thermal stability contribute to the safety and durability of plastic materials.
Used in Textile Industry:
In the textile industry, Phenyl tribromomethyl sulfone is utilized as a flame retardant to improve the fire safety of fabrics and garments. This ensures that textiles meet the required safety standards and reduces the risk of fire accidents.
Used in Electronics Industry:
Phenyl tribromomethyl sulfone is employed as a flame retardant in electronic components and devices to prevent fire hazards and ensure the safe operation of electronic systems.
Used in Pharmaceutical Research:
Due to its unique chemical properties, Phenyl tribromomethyl sulfone is being studied for potential applications in pharmaceuticals. Its exploration in this field is at a research stage, aiming to leverage its characteristics for developing new drugs or drug delivery systems.
Used in Other Industrial Applications:
Phenyl tribromomethyl sulfone's unique properties are also being investigated for use in other industrial applications beyond flame retardancy. The exploration of its potential uses is ongoing, driven by the need for innovative materials with specific chemical attributes.
Check Digit Verification of cas no
The CAS Registry Mumber 17025-47-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,2 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17025-47:
(7*1)+(6*7)+(5*0)+(4*2)+(3*5)+(2*4)+(1*7)=87
87 % 10 = 7
So 17025-47-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H5Br3O2S/c8-7(9,10)13(11,12)6-4-2-1-3-5-6/h1-5H
17025-47-7Relevant academic research and scientific papers
Controlled α-mono- and α,α-di-halogenation of alkyl sulfones using reagent-solvent halogen bonding
Poteat, Christopher M.,Lindsay, Vincent N. G.
, p. 2912 - 2915 (2019/03/17)
The direct and selective α-mono-bromination of alkyl sulfones was achieved through base-mediated electrophilic halogenation. The appropriate combination of solvent and electrophilic bromine source was found to be critical to control the nature of the products formed, where reagent-solvent halogen bonding is proposed to control the selectivity via alteration of the effective size of the electrophilic bromine source. Conversely, the α,α-di-brominated sulfones were selectively obtained in good yields following polyhalogenation followed by selective de-halogenation during workup. Both procedures can be applied on gram scale, and the mono-halogenation was successfully extended to the fully selective α-chlorination, α-iodination and α-fluorination of alkyl sulfones.
A simple and efficient synthesis of trihalomethyl and dihalonitromethyl aryl sulfones
Borys, Krzysztof M.,Korzynski, MacIej D.,Ochal, Zbigniew
, p. 6606 - 6610,5 (2012/12/12)
A method for the preparation of aryl trihalomethyl sulfones - active biocidal agents - with identical or different halogens is presented. The synthesis is based on the reaction of aryl methyl, aryl halomethyl, or aryl nitromethyl sulfones with sodium hypohalite. The method is simple in implementation, does not necessarily require the use of organic solvents, and selectively affords the products in good to excellent yields. Notably, it allows the preparation of the hitherto unknown phenyl trihalomethyl sulfone with three different halogens: fluorine, chlorine, and bromine.
