112995-48-9 Usage
Uses
Used in Polymer Industry:
ETHYL 2-(2,4,5-TRIBROMO-1H-IMIDAZOL-1-YL)ACETATE is used as a flame retardant for improving the fire resistance properties of various polymers. Its high thermal stability and low volatility contribute to the enhanced safety and durability of the polymers in which it is incorporated.
Used in Textile Industry:
In the textile industry, ETHYL 2-(2,4,5-TRIBROMO-1H-IMIDAZOL-1-YL)ACETATE is used as a flame retardant to enhance the fire resistance of fabrics and other textile products. This helps to protect the materials from catching fire and reduces the risk of fire-related accidents.
Used in Electronics Industry:
ETHYL 2-(2,4,5-TRIBROMO-1H-IMIDAZOL-1-YL)ACETATE is used in the electronics industry as a flame retardant to improve the fire safety of electronic components and devices. Its high thermal stability ensures that the components can withstand high temperatures without compromising their fire resistance properties.
Overall, ETHYL 2-(2,4,5-TRIBROMO-1H-IMIDAZOL-1-YL)ACETATE is considered to be relatively safe for human health and the environment when used properly, making it a valuable compound for various applications where flame resistance is crucial.
Check Digit Verification of cas no
The CAS Registry Mumber 112995-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,9,9 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 112995-48:
(8*1)+(7*1)+(6*2)+(5*9)+(4*9)+(3*5)+(2*4)+(1*8)=139
139 % 10 = 9
So 112995-48-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H7Br3N2O2/c1-2-14-4(13)3-12-6(9)5(8)11-7(12)10/h2-3H2,1H3
112995-48-9Relevant academic research and scientific papers
Azoles. Part 4. Nucleophilic Substitution Reactions of Halogenoimidazoles
Iddon, Brian,Khan, Nazir,Lim, Bee Lan
, p. 1437 - 1444 (2007/10/02)
A number of N-protected derivatives of 2,4,5-tribromoimidazole, 4(5)-bromo-5(4)-nitroimidazole, and 2,4(5)-dibromo-5(4)-nitroimidazole have been prepared by standard procedures and treated with various nucleophiles.Whereas 2,4,5-tribromo (and tri-iodo)imidazole reacted with sodium benzenethiolate to give the corresponding 4,5-dihalogenoimidazole and diphenyl disulphide, 1-protected derivatives of 2,4,5-tribromoimidazole reacted with various sodium alkane (or arene)thiolates and with sodium isopropoxide, in isoprpopyl alcohol, by displacement of the 2-bromine atom. 1-Benzyl-5-bromo-4-nitroimidazole (14), 2-(5-bromo-4-nitroimidazol-1-yl)acetate (25), and 5-bromo-4-nitro-1-phenacylimidazole (26) reacted by displacement of the 5-bromine atom.The product arising from reaction of the last compound with ethyl 2-mercaptoacetate in ethanol in the presence of base, cyclised to give ethyl 3-hydroxy-7-nitro-3-phenylimidazolothiazine-2-carboxylate (35).
