112995-48-9 Usage
General Description
ETHYL 2-(2,4,5-TRIBROMO-1H-IMIDAZOL-1-YL)ACETATE is a chemical compound with the formula C7H7Br3N2O2. It is a colorless to pale yellow liquid that is commonly used as a flame retardant in various applications. ETHYL 2-(2,4,5-TRIBROMO-1H-IMIDAZOL-1-YL)ACETATE is highly stable and has a low volatility, making it suitable for use in materials that require long-term flame resistance. It is also known for its high thermal stability and ability to withstand harsh environmental conditions. ETHYL 2-(2,4,5-TRIBROMO-1H-IMIDAZOL-1-YL)ACETATE is commonly used in the production of polymers, textiles, and electronics to improve their fire resistance properties. Additionally, it is considered to be relatively safe for human health and the environment when used properly.
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 articles and documents
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).
