ChemicalBook > CAS DataBase List > 4-[4-(TRIFLUOROMETHOXY)PHENOXY]PIPERIDINE

4-[4-(TRIFLUOROMETHOXY)PHENOXY]PIPERIDINE

Product Name
4-[4-(TRIFLUOROMETHOXY)PHENOXY]PIPERIDINE
CAS No.
287952-67-4
Chemical Name
4-[4-(TRIFLUOROMETHOXY)PHENOXY]PIPERIDINE
Synonyms
Delamanid intermediate;Piperidine, 4-[4-(trifluoroMethoxy)phenoxy]-;4-[4-(TrifluoroMethoxy)phenoxy]piperidine HCl
CBNumber
CB31476863
Molecular Formula
C12H14F3NO2
Formula Weight
261.24
MOL File
287952-67-4.mol
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4-[4-(TRIFLUOROMETHOXY)PHENOXY]PIPERIDINE Property

Melting point:
71-73℃
Boiling point:
292.2±40.0 °C(Predicted)
Density 
1.230±0.06 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
form 
powder to crystal
pka
9.65±0.10(Predicted)
color 
White to Light yellow
InChI
InChI=1S/C12H14F3NO2/c13-12(14,15)18-11-3-1-9(2-4-11)17-10-5-7-16-8-6-10/h1-4,10,16H,5-8H2
InChIKey
RPQOTFPZKNHYFB-UHFFFAOYSA-N
SMILES
N1CCC(OC2=CC=C(OC(F)(F)F)C=C2)CC1
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Safety

Hazard Codes 
Xn
Risk Statements 
22
HS Code 
2933.39.9200
HazardClass 
IRRITANT
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P405Store locked up.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
MNO000104
Product name
4-[4-(Trifluoromethoxy)phenoxy]piperidine
Purity
Aldrich
Packaging
1g
Price
$216
Updated
2025/07/31
TCI Chemical
Product number
T3349
Product name
4-[4-(Trifluoromethoxy)phenoxy]piperidine
Purity
>97.0%(GC)(T)
Packaging
1g
Price
$48
Updated
2025/07/31
TCI Chemical
Product number
T3349
Product name
4-[4-(Trifluoromethoxy)phenoxy]piperidine
Purity
>97.0%(GC)(T)
Packaging
5g
Price
$235
Updated
2025/07/31
TRC
Product number
T790890
Product name
4-[4-(Trifluoromethoxy)phenoxy]piperidine
Packaging
5g
Price
$415
Updated
2021/12/16
Medical Isotopes, Inc.
Product number
49059
Product name
4-[4-(Trifluoromethoxy)phenoxy]piperidine
Packaging
1g
Price
$625
Updated
2021/12/16
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4-[4-(TRIFLUOROMETHOXY)PHENOXY]PIPERIDINE Chemical Properties,Usage,Production

Uses

4-[4-(Trifluoromethoxy)phenoxy]piperidine is used in the preparation of 3,5-disubstituted isoxazolines as antituberculosis agents.

Synthesis

828-27-3

65214-82-6

287952-67-4

GENERAL STEPS: 9.72 kg of ethyl 4-hydroxypiperidine-1-carboxylate and 10.0 L of triethylamine were dissolved in 15.0 L of toluene and the resulting solution was cooled to below 10 °C. To this solution, 7.07 kg of methanesulfonyl chloride was slowly added dropwise at a temperature below 25 °C, followed by continued stirring for 1 hour at below 25 °C. Next, 5.00 kg of 4-trifluoromethoxyphenol, 10 L of toluene, 17.7 L of 25% aqueous sodium hydroxide and 6.24 kg of 50% aqueous tetra-n-butyl ammonium chloride were added to the reaction solution. The mixture was heated to reflux for 2 hours (internal temperature was maintained at 88°C). After completion of the reaction, the mixture was cooled and the aqueous layer was separated and discarded. The organic layer was washed with 10 L of water. Subsequently, 14.2 kg of potassium hydroxide and 10 L of ethanol were added to the washed organic layer and the mixture was heated to reflux for 4 hours (internal temperature maintained at 98 °C). After cooling, concentration was carried out under reduced pressure. To the concentrated residue, 50 L of toluene was added and the organic layer was washed sequentially with 25 L of water, 25 L of brine and 31 L of aqueous ammonium chloride. The washed toluene solution was concentrated under reduced pressure. The concentrated residue was dissolved in a solvent mixture of 5 L of isopropanol, 50 L of water and 2.5 L of 25% aqueous sodium hydroxide to form a homogeneous solution, which was subsequently cooled to below 10 °C. After the crystals precipitated, stirring was continued below 10 °C for 1 h. The precipitate was then collected by filtration. The crystals were washed with 15 L of water and dried in air to give 6.67 kg of 4-(4-trifluoromethoxyphenoxy)piperidine (isolated yield: 90.9%). 1H-NMR (300 MHz, CDCl3) δ ppm: 1.41 (2H, dddd), 1.90 (2H, m), 2.55 (2H, dddd), 2.92 (2H, dddd), 3.33 (1H, brs), 4.39 (1H, tt), 7.03 (2H, d), 7.25 (2H, d).

References

[1] Patent: US2018/65931, 2018, A1. Location in patent: Paragraph 0135

4-[4-(TRIFLUOROMETHOXY)PHENOXY]PIPERIDINE Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from 4-[4-(TRIFLUOROMETHOXY)PHENOXY]PIPERIDINE manufacturers

Henan Aochuang Chemical Co.,Ltd.
Product
4-[4-(trifluoromethoxy)phenoxy]piperidine 287952-67-4
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
98%
Supply Ability
1Ton
Release date
2022-09-30
Shanghai CRM New Material Technology Co., LTD
Product
4-(4-Trifluoromethoxyphenoxy)piperidine 287952-67-4
Price
US $10.00-15.00/g
Min. Order
10g
Purity
99%
Supply Ability
10t
Release date
2022-09-21
Career Henan Chemical Co
Product
4-[4-(TRIFLUOROMETHOXY)PHENOXY]PIPERIDINE 287952-67-4
Price
US $9.80/KG
Min. Order
1g
Purity
≥99%
Supply Ability
100kg
Release date
2019-12-26

287952-67-4, 4-[4-(TRIFLUOROMETHOXY)PHENOXY]PIPERIDINERelated Search:


  • Piperidine, 4-[4-(trifluoroMethoxy)phenoxy]-
  • 4-[4-(TrifluoroMethoxy)phenoxy]piperidine HCl
  • Delamanid intermediate
  • 287952-67-4