3555-18-8

Usage

Uses

Used in Pharmaceutical Industry:
4-(1-methylpropyl)-2-nitrophenol is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows it to be incorporated into the development of new drugs, potentially leading to innovative treatments and therapies.
Used in Agrochemical Industry:
In the agrochemical industry, 4-(1-methylpropyl)-2-nitrophenol serves as an intermediate in the production of various agrochemicals. Its incorporation into these products can contribute to the development of more effective and targeted pest control solutions, enhancing crop protection and yield.
Used in Dye and Pigment Production:
4-(1-methylpropyl)-2-nitrophenol is utilized as an intermediate in the manufacturing of dyes and pigments. Its chemical properties enable the creation of a wide range of colors and shades, offering versatility in various applications such as textiles, plastics, and inks.
Environmental and Safety Considerations:
Due to its toxic nature and potential environmental hazards, 4-(1-methylpropyl)-2-nitrophenol requires careful handling and disposal. Proper safety measures, including the use of personal protective equipment and adherence to waste management regulations, should be implemented to minimize risks to human health and the environment.

InChI:InChI=1/C10H13NO3/c1-3-7(2)8-4-5-10(12)9(6-8)11(13)14/h4-7,12H,3H2,1-2H3

Upstream product

• 99-71-8 4-(1-methylpropyl)phenol 
• 108-95-2 phenol 

Downstream Products

• 74752-33-3 O-4-sec-Butyl-2-nitrophenyl Dimethylcarbamothioate 
• 3280-71-5 2-Amino-4-sec-butyl-phenol 
• 74752-45-7 β-D-Glucopyranosyl 4-sec-Butyl-2-nitrophenyl Disulfide 
• 74752-36-6 S-4-sec-Butyl-2-nitrophenyl Dimethylcarbamothioate 
• 74752-42-4 4-sec-Butyl-2-nitrobenzenesulfenyl Chloride 
• 74752-39-9 4-sec-Butyl-2-nitrothiophenol 
• 1129-27-7 4-(1-methylpropyl)benzene-1,2-diol 

Relevant academic research and scientific papers

Nitration method for p-alkylphenol

The invention discloses a nitration method for p-alkylphenol. The nitration method successively comprises the following steps: 1) adding the p-alkylphenol used as a raw material into a container, thenadding water and a catalyst, dropwise adding nitric acid under stirring, controlling a temperature of materials in the container not to exceed 25 DEG C in the dropwise adding process, and after the nitric acid is dropwise added, carrying out a reaction at 10 to 20 DEG C for 2 to 3 h; and 2) subjecting a reaction solution obtained in the step 1) to standing and layering, wherein the lower layer obtained by layering is a product (o-nitro-p-alkylphenol), and subjecting an upper-layer solution obtained by layering to cyclic reuse, i.e., cyclic nitration. By adoption of the method for synthesizingthe o-nitro-p-alkylphenol provided by the invention, the utilization rate of raw materials is high; cyclic reuse of waste acid and waste water is realized; the discharging of three wastes is reduced;the cost of production is lowered; meanwhile, a product has high purity, high yield and good industrial application value.

Alkyl-substituted benzoxazinorifamycin derivative, process for preparing the same and antibacterial agent containing the same

A novel rifamycin derivative having the formula (I): STR1 wherein X1 is an alkyl group with 1 to 6 carbon atoms or a cycloalkyl group with 3 to 8 carbon atoms; X2 is a hydrogen atom or an alkyl group with 1 to 4 carbon atoms; R1 is hydrogen atom or acetyl group; A is a group represented by the formula: STR2 wherein R2 is an alkyl group with 1 to 4 carbon atoms or an alkoxyalkyl group with 2 to 6 carbon atoms and R3 is an alkyl group with 1 to 6 carbon atoms or an alkoxyalkyl group with 2 to 6 carbon atoms, or a group represented by the formula STR3 wherein STR4 is a 3 to 9 membered cyclic amino group with 2 to 8 carbon atoms, R4 is a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, or salts thereof, a process for preparing the same and antibacterial agents containing the same as an effective ingredient. The rifamycin derivative of the present invention having the formula (I) shows a strong antibacterial activity against the Gram-positive bacteria and the acid-fast bacteria.