
288573-56-8
- Product Name:1-BOC-4-(4-FLUORO-PHENYLAMINO)-PIPERIDINE,Tert-Butyl 4-[(4-Fluorophenyl)Amino]Piperidine-1-Carboxylate
- Molecular Formula:C16H23 F N2 O2
- Purity:99%
- Molecular Weight:294.369
Product Details
Hot Sale! We supply high quality High Purity 99% Pharmaceutical Intermediates Tert-Butyl 4-[(4-Fluorophenyl)Amino]Piperidine-1-Carboxylate (CAS 288573-56-8), in stock, Good Manufacturer, Fast Delivery factory directly supply to clients, wholesale price, more competitiveness.
What is the 1-BOC-4-(4-FLUORO-PHENYLAMINO)-PIPERIDINE ?
Tert-Butyl 4-[(4-Fluorophenyl)Amino]Piperidine-1-Carboxylate specifications is a heterocyclic derivative, while it's Molecular Formula is C16H23 F N2 O2. 1-BOC-4-(4-FLUORO-PHENYLAMINO)-PIPERIDINE is a heterocyclic derivative and can be used as a pharmaceutical intermediate.
What is the CAS number for 1-BOC-4-(4-FLUORO-PHENYLAMINO)-PIPERIDINE ?
The CAS number of 1-BOC-4-(4-FLUORO-PHENYLAMINO)-PIPERIDINE is 288573-56-8.
More information of 1-BOC-4-(4-FLUORO-PHENYLAMINO)-PIPERIDINE 288573-56-8 are:
Synonyms |
1-tert-Butoxycarbonyl-4-[(4-fluorophenyl)amino]piperidine;4-(4-Fluorophenylamino)piperidine-1-carboxylic acid tert-butyl ester;tert-Butyl 4-(4-fluoroanilino)-1-piperidinecarboxylate |
CAS Number |
288573-56-8 |
Molecular Formula |
C16H23 F N2 O2 |
Molecular Weight |
294.369 |
Density |
1.159±0.06 g/cm3(Predicted) |
Boiling Point |
400.4±40.0 °C(Predicted) |
PSA |
41.57000 |
LogP |
3.64800 |
Pka |
5.09±0.20(Predicted) |
What is 1-BOC-4-(4-FLUORO-PHENYLAMINO)-PIPERIDINE (288573-56-8) used for?
1-BOC-4-(4-FLUORO-PHENYLAMINO)-PIPERIDINE is used as a pharmaceutical intermediate.
Articles related to 1-BOC-4-(4-FLUORO-PHENYLAMINO)-PIPERIDINE:
Article |
Source |
Dual targeting of acetylcholinesterase and tau aggregation: Design, synthesis and evaluation of multifunctional deoxyvasicinone analogues for Alzheimer's disease |
Manzoor, Shoaib,Gabr, Moustafa T.,Rasool, Bisma,Pal, Kavita,Hoda, Nasimul , (2021/09/28) |
Intermediates to a copper bisoxazoline catalyst for asymmetric synthesis of agrochemical or pharmaceutical intermediates such as insecticides; reacting a cycloalkylidenemalonic diester with an aminoalcohol to form amide intermediate; cyclization to ligand | M Itagaki US20070112201 A1 |
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