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1,3-Piperidinedicarboxylic acid, 4-(4-fluorophenyl)-, 1-(1,1-dimethylethyl) ester, (3S,4R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

923932-21-2

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  • (3S,4R)-1-(TERT-BUTOXYCARBONYL)-4-(4-FLUOROPHENYL)PIPERIDINE-3-CARBOXYLIC ACID

    Cas No: 923932-21-2

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923932-21-2 Usage

Molecular weight

329.39 g/mol

Appearance

White crystalline powder

Stereochemistry

(3S,4R)-

Parent compound

1,3-Piperidinedicarboxylic acid

Substituents

a. 4-(4-fluorophenyl) group
b. 1-(1,1-dimethylethyl) ester group

Biological activity

Modulator of neurotransmitter receptors

Applications

a. Building block in the synthesis of pharmaceutical and agrochemical products
b. Potential use in the development of new medications for neurological disorders
c. Reagent in organic synthesis and medicinal chemistry research

Check Digit Verification of cas no

The CAS Registry Mumber 923932-21-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,3,9,3 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 923932-21:
(8*9)+(7*2)+(6*3)+(5*9)+(4*3)+(3*2)+(2*2)+(1*1)=172
172 % 10 = 2
So 923932-21-2 is a valid CAS Registry Number.

923932-21-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,4R)-4-(4-fluorophenyl)-1-[(2-methylpropan-2-yl)oxycarbonyl]piperidine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-tert-butyl (3S,4R)-4-(4-fluoro-phenyl)-piperidine-1,3-dicarboxylate

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:923932-21-2 SDS

923932-21-2Relevant articles and documents

CCR2 MODULATORS

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, (2016/12/07)

Compounds are provided that are modulators of the CCR2 receptor. The compounds have the general formula (I) and are useful in pharmaceutical compositions, methods for the treatment of diseases and disorders involving the pathologic activtation of CCR2 receptors.

PIPERAZINE AMIDE DERIVATIVES

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Page/Page column 23, (2009/03/07)

The invention is concerned with novel piperazine amide derivatives of formula (I) wherein R1 to R11, W, X and Y are as defined in the description and in the claims, as well as physiologically acceptable salts thereof. These compounds bind to LXR alpha and LXR beta and can be used as medicaments.

Process for the preparation of enantiomerically enriched cyclic beta-aryl or heteroaryl carbocyclic acids

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Page/Page column 33, (2008/06/13)

The present invention relates to a process for the preparation of cis substituted cyclic β-aryl or heteroaryl carboxylic acid derivatives in high diastereo- and enantioselectivity by enantioselective hydrogenation in accordance with the following scheme w

Serotonin transporter (sert) inhibitors for the treatment of depression and anxiety

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Page/Page column 14, (2008/06/13)

The present invention relates to trans-derivatives of formula wherein R1, R2, R3, and the dotted line are as defined herein and to pharmaceutically acceptable acid addition salts thereof. The compounds of formula I are goo

NOVEL BENZO [D] [1,3]-DIOXOL DERIVATIVES

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Page/Page column 56, (2010/11/25)

The present invention relates to an isotopologue of Compound 1 substituted with deuterium at the methylene carbon of the benzodioxol ring. The isotopologues of this invention selective serotonin reuptake inhibitors (SSRIs) and possess unique biopharmaceutical and metabolic properties compared to Compound 1. They may also be used to accurately determine the concentration of Compound 1 in biological fluids and to determine metabolic patterns of Compound 1 and its isotopologues. The invention further provides compositions comprising these deuterated isotopologues and methods of treating diseases and conditions that are responsive to increased neuronal serotonin transmission, alone and in combination with additional agents.

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