4097-53-4 Usage
Description
3,5-DINITRO-BIPHENYL-4-OL is a chemical compound with the molecular formula C12H8N2O5, derived from biphenyl and containing two nitro groups and a hydroxyl group attached to the fourth carbon of one of the benzene rings. It is known for its high toxicity and is classified as a hazardous substance, posing health risks to humans and potential harm to the environment.
Uses
Due to the high toxicity and hazardous nature of 3,5-DINITRO-BIPHENYL-4-OL, its uses are limited and strictly regulated. However, it may be used in specific applications such as:
Used in Chemical Research:
3,5-DINITRO-BIPHENYL-4-OL is used as a research compound for studying its chemical properties and potential applications in various fields. It is important to handle and store this substance with extreme caution to prevent any adverse effects on health and the environment.
Used in Environmental Monitoring:
3,5-DINITRO-BIPHENYL-4-OL may be used as a reference substance in environmental monitoring programs to detect and measure the presence of hazardous chemicals in the environment. This can help in assessing the risks associated with exposure to such substances and implementing appropriate safety measures.
It is crucial to note that the use of 3,5-DINITRO-BIPHENYL-4-OL should be strictly controlled and limited to minimize its potential harmful effects on health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 4097-53-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,9 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4097-53:
(6*4)+(5*0)+(4*9)+(3*7)+(2*5)+(1*3)=94
94 % 10 = 4
So 4097-53-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H8N2O5/c15-12-10(13(16)17)6-9(7-11(12)14(18)19)8-4-2-1-3-5-8/h1-7,15H
4097-53-4Relevant articles and documents
Hydroxynitrobiphenyls produced by photochemical reaction of biphenyl in aqueous nitrate solution and their mutagenicities
Suzuki,Sato,Suzuki
, p. 2507 - 2515 (1985)
From the photoreaction products of biphenyl in aqueous nitrate solution, the following eight hydroxynitrobiphenyls were isolated by silica gel column chromatography and thin layer chromatography on silica gel and polyamide plates: 4-hydroxy-3,5-dinitrobiphenyl (F1(2)or), 4,2'-dihydroxy-3,3'-dinitrobiphenyl (F4(1)-3), 4-hydroxy-3,3'-dinitrobiphenyl (F4(1)-4), a hydroxydinitrobiphenyl (F4(1)-5a), 4,4'-dihydroxy-3,3'-dinitrobiphenyl (F4(1)-5b), a dihydroxydinitrobiphenyl (F4(1)-6), 2-hydroxy-3-nitrobiphenyl (F5(1)) and 4-hydroxy-3-nitrobiphenyl (F5(2)). Among these compounds, four dinitro compounds, F1(2)or, F4(1)-4, F4(1)-5a and F4(1)-6, exhibited mutagenicity toward S. typhimurium TA98 without S-9 mix. The major products in this reaction were nitrophenylphenols, F5(1) and F5(2), and these were non-mutagenic. The major mutagens, F4(1)-5a and F4(1)-6, were produced in such small amounts that the exact structures could not be determined. The mechanism of production of these hydroxynitrobiphenyls is discussed on the basis of the results of analysis of the reaction mixture by high-performance liquid chromatography.