62559-08-4

Basic information

• Product Name: 4-tert-butyl-1-methyl-2-nitrobenzene
• Synonyms: 4-tert-butyl-1-methyl-2-nitrobenzene
• CAS NO: 62559-08-4
• Molecular Formula: C₁₁H₁₅NO₂
• Molecular Weight: 193.2423
• Mol File: 62559-08-4.mol
• Article Data: 17

Chemical Properties

• Boiling Point: 140 °C
• Appearance: /
• Density: 1.0514 g/cm3(Temp: 21 °C)
• CAS DataBase Reference: 4-tert-butyl-1-methyl-2-nitrobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 4-tert-butyl-1-methyl-2-nitrobenzene(62559-08-4)
• EPA Substance Registry System: 4-tert-butyl-1-methyl-2-nitrobenzene(62559-08-4)

Safety Data

• Hazardous Substances Data: 62559-08-4(Hazardous Substances Data)

Upstream product

• 7664-93-9 sulfuric acid 
• 98-51-1 4-tert-butyltoluene 
• 7697-37-2 nitric acid 

Downstream Products

• 96864-00-5 4-(1,1-dimethylethyl)-2-nitrobenzaldehyde 
• 263843-05-6 dimethylsulfamic acid 4-{6-[2-(4-aminophenyl)ethyl]-4-hydroxy-6-isopropyl-2-oxo-5,6-dihydro-2H-pyran-3-ylsulfanyl}-5-tert-butyl-2-methylphenyl ester hydrochloride 
• 5781-02-2 5-(tert-butyl)-2-methylphenol 
• 207737-16-4 5-tert-butyl-4-mercapto-2-methylphenol 
• 207737-07-3 5-tert-butyl-2-methyl-4-thiocyanatophenol 
• 207737-17-5 toluene-4-thiosulfonic acid S-(2-tert-butyl-4-hydroxy-5-methylphenyl) ester 
• 207737-25-5 5-tert-butyl-2-methyl-4-thiocyanatophenylamine 
• 207737-20-0 toluene-4-thiosulfonic acid S-(2-tert-butyl-4-dimethylsulfamoyloxy-5-methyl-phenyl) ester 
• 207737-21-1 toluene-4-thiosulfonic acid S-(2-tert-butyl-4-ethylsulfamoyloxy-5-methyl-phenyl) ester 
• 249728-23-2 ethyl-sulfamic acid 5-tert-butyl-4-(4-hydroxy-6-isopropyl-2-oxo-6-phenethyl-5,6-dihydro-2H-pyran-3-ylsulfanyl)-2-methyl-phenyl ester 
• 249728-17-4 dimethyl-sulfamic acid 5-tert-butyl-4-{4-hydroxy-6-[2-(4-hydroxy-phenyl)-ethyl]-6-isopropyl-2-oxo-5,6-dihydro-2H-pyran-3-ylsulfanyl}-2-methyl-phenyl ester 
• 207736-26-3 ethyl-sulfamic acid 5-tert-butyl-4-{4-hydroxy-6-[2-(4-hydroxy-phenyl)-ethyl]-6-isopropyl-2-oxo-5,6-dihydro-2H-pyran-3-ylsulfanyl}-2-methyl-phenyl ester 
• 260257-94-1 3-(2-tert-butyl-4-hydroxy-5-methyl-phenylsulfanyl)-4-hydroxy-6-isopropyl-6-phenethyl-5,6-dihydro-pyran-2-one 

Relevant articles and documents

METHOD FOR CONVERTING HYDROXYL GROUP OF ALCOHOL

The present invention relates to: a method for converting a hydroxyl group of an alcohol; and a catalyst which makes the method possible. A method for converting a hydroxyl group of an alcohol according to the present invention is characterized by producing a compound represented by CH(R1)(R2)Nu (wherein R1, R2 and Nu are as defined below) by reacting an alcohol represented by CH(R1)(R2)OH (wherein each of R1 and R2 represents a hydrogen atom, an optionally substituted alkyl group, or the like) and a compound having an active proton, which is represented by H-Nu (wherein Nu represents a group represented by —CHX1-EWG1 or —NR3R4; X1 represents a hydrogen atom or the like; EWG1 represents an electron-withdrawing group; and each of R3 and R4 represents a hydrogen atom, an optionally substituted alkyl group, or the like), with each other in the presence of a complex of a group 7-11 metal of the periodic table and at least one solid base that is selected from the group consisting of layered double hydroxides, composite oxides and calcium hydroxide.

DUAL AGONISTS OF FXR AND PPARδ AND THEIR USES

The present invention relates to small molecule compounds and their use as agonists of farnesoid X receptor (FXR) and/or peroxisome proliferator activated receptor delta (PPARδ). The present invention also relates to the use of said compounds in the treatment of metabolic diseases and respective methods of treatment.

Meta-Oligoazobiphenyls - Synthesis via site-selective Mills reaction and photochemical properties

The investigation of multi-photochromic compounds constitutes a great challenge, not only from a synthetic point of view, but also with respect to the analysis of the photochemical properties. In this context we designed a novel strategy to access meta-ol