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7576-09-2

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7576-09-2 Usage

Chemical compound

1-benzyl-4-tert-butylpiperidine is a chemical compound with the molecular formula C17H27N.

Type

It is a piperidine derivative.

Common uses

It is commonly used as an intermediate in the synthesis of pharmaceuticals.

Synonyms

1-benzyl-4-tert-butylpiperidine is also known as Lu 2-11 or DOV-102,677.

Potential applications

It has been studied for its potential use as a treatment for various neurological and psychiatric disorders.

Preclinical studies

1-benzyl-4-tert-butylpiperidine has shown promise in preclinical studies for its ability to modulate neurotransmitter systems in the brain.

Interaction with receptors

It particularly interacts with dopamine and serotonin receptors.

Further research

More research is needed to fully understand its pharmacological effects and potential therapeutic uses.

Check Digit Verification of cas no

The CAS Registry Mumber 7576-09-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,7 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7576-09:
(6*7)+(5*5)+(4*7)+(3*6)+(2*0)+(1*9)=122
122 % 10 = 2
So 7576-09-2 is a valid CAS Registry Number.

7576-09-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-4-tert-butylpiperidine

1.2 Other means of identification

Product number -
Other names 1-Benzyl-4-tert.-butyl-piperidin

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:7576-09-2 SDS

7576-09-2Relevant articles and documents

Stereoselective Nucleophilic Addition to Conformationally Constrained Piperidines. An Efficient Route to 2-Axial-6-Equatorial Disubstituted Piperidines.

Meyers, A. I.,Shawe, Thomas T.,Gottlieb, Levi

, p. 867 - 870 (2007/10/02)

Addition of RMgX to 2-methoxy-4-tert-butylpiperidine formamidine in dichloromethane or ether gives good to excellent yields of axial product.

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