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N-(4-fluorophenyl)piperidine-1-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60465-12-5

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60465-12-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60465-12-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,6 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60465-12:
(7*6)+(6*0)+(5*4)+(4*6)+(3*5)+(2*1)+(1*2)=105
105 % 10 = 5
So 60465-12-5 is a valid CAS Registry Number.

60465-12-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-fluorophenyl)piperidine-1-carboxamide

1.2 Other means of identification

Product number -
Other names 4'-Fluoro-1-piperidinecarboxanilide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:60465-12-5 SDS

60465-12-5Downstream Products

60465-12-5Relevant academic research and scientific papers

Synthesis of 11C-labelled ureas by palladium(II)-mediated oxidative carbonylation

Roslin, Sara,Brandt, Peter,Nordeman, Patrik,Larhed, Mats,Odell, Luke R.,Erikssoni, Jonas

, (2017/11/07)

Positron emission tomography is an imaging technique with applications in clinical settings as well as in basic research for the study of biological processes. A PET tracer, a biologically active molecule where a positron-emitting radioisotope such as carbon-11 has been incorporated, is used for the studies. Development of robust methods for incorporation of the radioisotope is therefore of the utmost importance. The urea functional group is present in many biologically active compounds and is thus an attractive target for incorporation of carbon-11 in the form of [11C]carbon monoxide. Starting with amines and [11C]carbon monoxide, both symmetrical and unsymmetrical 11C-labelled ureas were synthesised via a palladium(II)-mediated oxidative carbonylation and obtained in decay-corrected radiochemical yields up to 65%. The added advantage of using [11C]carbon monoxide was shown by the molar activity obtained for an inhibitor of soluble epoxide hydrolase (247 GBq/μmol-319 GBq/μ mol). DFT calculations were found to support a reaction mechanism proceeding through an 11C-labelled isocyanate intermediate.

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