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1-BOC-3-[(2-FLUORO-PHENYLAMINO)-METHYL]-PIPERIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

309747-94-2

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309747-94-2 Usage

Chemical class

Piperidine derivatives
A class of chemical compounds containing a piperidine ring.

Structure

Piperidine ring
A six-membered heterocyclic ring with one nitrogen atom and five carbon atoms.

Protecting group

BOC (tert-butyloxycarbonyl)
A bulky group attached to the nitrogen atom of the piperidine ring, protecting it from unwanted reactions.

Substituent

2-fluoro-phenylamino-methyl group
A functional group containing a 2-fluorophenyl ring and an aminomethyl moiety attached to one of the carbon atoms of the piperidine ring.

Potential applications

Medicinal chemistry and pharmaceutical research
Due to the diverse biological activities exhibited by piperidine derivatives, 1-BOC-3-[(2-FLUORO-PHENYLAMINO)-METHYL]-PIPERIDINE may have therapeutic potential.

Reactivity manipulation

BOC protecting group
The presence of the BOC group allows for control over the compound's reactivity, enabling selective reactions and synthesis.

Pharmacological properties

Fluorophenyl group
The 2-fluorophenyl group may contribute to the compound's pharmacological properties, affecting its interactions with biological targets.

Synthesis building block

Novel bioactive molecules
1-BOC-3-[(2-FLUORO-PHENYLAMINO)-METHYL]-PIPERIDINE can be used as a building block in the synthesis of new bioactive molecules with therapeutic potential.

Check Digit Verification of cas no

The CAS Registry Mumber 309747-94-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,9,7,4 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 309747-94:
(8*3)+(7*0)+(6*9)+(5*7)+(4*4)+(3*7)+(2*9)+(1*4)=172
172 % 10 = 2
So 309747-94-2 is a valid CAS Registry Number.

309747-94-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 3-[(2-fluoroanilino)methyl]piperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:309747-94-2 SDS

309747-94-2Upstream product

309747-94-2Relevant academic research and scientific papers

Heterocyclic analgesic compounds and methods of use thereof

-

, (2008/06/13)

One aspect of the present invention relates to novel heterocyclic compounds. A second aspect of the present invention relates to the use of the novel heterocyclic compounds as ligands for various cellular receptors, including opiate receptors, other G-protein-coupled receptors, and ion channels. An additional aspect of the present invention relates to the use of the novel heterocyclic compounds as analgesics.

Heterocyclic analgesic compounds and methods of use thereof

-

, (2008/06/13)

One aspect of the present invention relates to novel heterocyclic compounds. A second aspect of the present invention relates to the use of the novel heterocyclic compounds as ligands for various cellular receptors, including opiate receptors, other G-protein-coupled receptors, and ion channels. An additional aspect of the present invention relates to the use of the novel heterocyclic compounds as analgesics.

Heterocyclic analgesic compounds and methods of use thereof

-

, (2008/06/13)

One aspect of the present invention relates to novel heterocyclic compounds. A second aspect of the present invention relates to the use of the novel heterocyclic compounds as ligands for various cellular receptors, including opiate receptors, other G-protein-coupled receptors, and ion channels. An additional aspect of the present invention relates to the use of the novel heterocyclic compounds as analgesics.

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