866109-93-5

Basic information

• Product Name: Phenol, 4-[4-[4-(trifluoroMethoxy)phenoxy]-1-piperidinyl]-, 4-Methylbenzenesulfonate (salt)
• Synonyms: Phenol, 4-[4-[4-(trifluoroMethoxy)phenoxy]-1-piperidinyl]-, 4-Methylbenzenesulfonate (salt);4-[4-(4-trifluoromethoxy phenoxy)-piperidin-1-yl] phenol p-toluene-4-sulfonic acid salt;Phenol, 4-[4-[4-(trifluoroMethoxy)phenoxy]-1-piperidinyl]-, 4-Methylbenzenesulfonate
• CAS NO: 866109-93-5
• Molecular Formula: C₇H₈O₃S*C₁₈H₁₈F₃NO₃
• Molecular Weight: 525.5372496
• EINECS: -0
• Mol File: 866109-93-5.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Phenol, 4-[4-[4-(trifluoroMethoxy)phenoxy]-1-piperidinyl]-, 4-Methylbenzenesulfonate (salt)(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 4-[4-[4-(trifluoroMethoxy)phenoxy]-1-piperidinyl]-, 4-Methylbenzenesulfonate (salt)(866109-93-5)
• EPA Substance Registry System: Phenol, 4-[4-[4-(trifluoroMethoxy)phenoxy]-1-piperidinyl]-, 4-Methylbenzenesulfonate (salt)(866109-93-5)

Safety Data

• Hazardous Substances Data: 866109-93-5(Hazardous Substances Data)

Upstream product

• 681482-80-4 1-[4-(tetrahydropyran-2-yloxy)phenyl]-4-(4-trifluoromethoxyphenoxy)piperidine 
• 104-15-4 toluene-4-sulfonic acid 
• 637-88-7 1,4-Cyclohexanedione 
• 287952-67-4 4-(4-(trifluoromethoxy)phenoxy)piperidine 
• 681482-81-5 1-(4-hydroxyphenyl)-4-(4-trifluoromethoxyphenoxy)piperidine 

Downstream Products

• 1083099-35-7 (R)-1-(4-((2-methyloxiran-2-yl)-methoxy)phenyl)-4-(4-(trifluoro-methoxy)phenoxy)piperidine 
• 681482-81-5 1-(4-hydroxyphenyl)-4-(4-trifluoromethoxyphenoxy)piperidine 

Relevant articles and documents

Preparation method of aromatic amine intermediate

The invention discloses a preparation method of an aromatic amine intermediate. The preparation method comprises the following steps: 1, in a polar aprotic solvent, under the presence of a catalyst, aligand and an alkali, a compound of formula III and a c

METHOD OF PRODUCING AMINOPHENOL COMPOUNDS

The present invention provides an industrially advantageous method of producing aminophenol compounds represented by the formula (1) by a simple and easy procedure at a high yield and a high purity. The present invention provides a method of producing an aminophenol compound represented by the formula (1): (wherein each of R1 and R2, which may be the same or different, is a hydrogen atom, a substituted or unsubstituted lower alkyl group or the like; R1 and R2, taken together with the adjacent nitrogen atom, may form a 5- or 6-membered heterocycle with or without other intervening heteroatoms; the heterocycle may be substituted by 1 to 3 substituents selected from the group consisting of a hydroxyl group, a substituted or unsubstituted lower alkyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted aryloxy group and the like; and the hydroxyl group in the formula (1) is substituted on the 2- or 4-position to the amino group on the phenyl ring), which comprises allowing a cyclohexanedione compound represented by the formula (2) to react with an amine compound represented by the formula (3) (wherein R1 and R2 are as defined above), under a neutral or basic condition.