Newblue-chem_1-TRIFLUOROACETYL PIPERIDINE,340-07-8

Min.Order / FOB Price:Get Latest Price

1 Kilogram	Negotiable

1 Kilogram

Negotiable

Min.Order :1 Kilogram
Purity: 90.0%Min
Payment Terms : T/T,

Keywords

340-07-8 1-TRIFLUOROACETYL PIPERIDINE 340-07-8

Quick Details

Appearance:liquid
Application:For pharmacy chemiacals
PackAge:as per buyer's request
ProductionCapacity:100|Kilogram|Month
Storage:Room Temperature
Transportation:By sea air

Superiority:

Our company was built in 2009 with an ISO certificate.In the past 5 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.Our main business covers the fields below:

1.Noble Metal Catalysts (Pt.Pd...)

2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...)

3.OLED intermediates (Fluorene,Carbazole,Boric acid...)

4.Customs Synthesis

Our advantage:

1. Higest quality and good package

2.Fast delivery

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5.Good business credit in Europe ,US ,Japan ,Korea

Anyway ,if you need any chemicals from China ,Henan Newblue can help you

Details:

Product Name: 1-TRIFLUOROACETYL PIPERIDINE

Synonyms: 1-Trifluoroacetyl piperidine 97%;1-TRIFLUOROACETYL PIPERIDINE;N-(Trifluoromethylacetyl)piperidine

CAS: 340-07-8

MF: C7H10F3NO

MW: 181.1556096

EINECS:

Product Categories: Miscellaneous Reagents;Building Blocks;Heterocyclic Building Blocks;Piperidines;Acids and Derivatives;Heterocycles;Piperidine;API intermediates

Mol File: 340-07-8.mol

1-TRIFLUOROACETYL PIPERIDINE Structure

1-TRIFLUOROACETYL PIPERIDINE Chemical Properties

Boiling point 77°C/15mmHg(lit.)

density 1.226 g/mL at 25 °C

refractive index n20/D 1.4171

Fp 77 °C

storage temp. Refrigerator

Safety Information

Hazard Codes T

Risk Statements 25-50

Safety Statements 45-61

RIDADR UN 2810

MSDS Information

1-TRIFLUOROACETYL PIPERIDINE Usage And Synthesis

Chemical Properties Light Yellow Oil

Uses N-Trifluoroacetylpiperidine is a reactant for synthesis of: photoreactive probes that differentiate the binding sites of noncompetitive GABA receptor antagonists; photoactive a-mannosides and mannosyl peptides; photoaffinity labeled fusidic acid analogues; hydroxyamides as anticonvulsants.

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