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4-(3-Fluoro-5-trifluoromethylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester is a piperazine derivative featuring a tert-butyl ester group attached to the carboxylic acid functional group. 4-(3-Fluoro-5-trifluoromethylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester incorporates a pyridine ring with a fluoro and trifluoromethyl substituent at specific positions, endowing it with distinctive structural and chemical characteristics. Piperazine derivatives are recognized for their biological activity and therapeutic potential, and the presence of the tert-butyl ester group enhances its solubility and bioavailability, making it a promising candidate for pharmaceutical research and development.

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  • 4-(3-Fluoro-5-trifluoromethylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester

    Cas No: 897376-76-0

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  • 4-(3-Fluoro-5-trifluoromethylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester

    Cas No: 897376-76-0

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  • 897376-76-0 Structure
  • Basic information

    1. Product Name: 4-(3-Fluoro-5-trifluoromethylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester
    2. Synonyms: 4-(3-Fluoro-5-trifluoromethylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester
    3. CAS NO:897376-76-0
    4. Molecular Formula: C15H19F4N3O2
    5. Molecular Weight: 349.3238728
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 897376-76-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-(3-Fluoro-5-trifluoromethylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(3-Fluoro-5-trifluoromethylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester(897376-76-0)
    11. EPA Substance Registry System: 4-(3-Fluoro-5-trifluoromethylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester(897376-76-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 897376-76-0(Hazardous Substances Data)

897376-76-0 Usage

Uses

Used in Pharmaceutical Research and Development:
4-(3-Fluoro-5-trifluoromethylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester is utilized as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure and the presence of the tert-butyl ester group contribute to its potential as a prodrug, which can be further developed to improve the solubility and bioavailability of the final drug product.
Used in Drug Formulation:
As a prodrug, 4-(3-Fluoro-5-trifluoromethylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester is used to enhance the solubility and bioavailability of active pharmaceutical ingredients. This can lead to improved drug delivery and therapeutic efficacy, making it a valuable component in the development of novel drug formulations.
Further study and investigation are necessary to fully explore the potential uses and effects of this chemical, as its specific applications and benefits in various industries are not yet fully understood.

Check Digit Verification of cas no

The CAS Registry Mumber 897376-76-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,7,3,7 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 897376-76:
(8*8)+(7*9)+(6*7)+(5*3)+(4*7)+(3*6)+(2*7)+(1*6)=250
250 % 10 = 0
So 897376-76-0 is a valid CAS Registry Number.

897376-76-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 4-[3-fluoro-5-(trifluoromethyl)pyridin-2-yl]piperazine-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:897376-76-0 SDS

897376-76-0Relevant articles and documents

MODULATORS OF METABOTROPIC GLUTAMATE RECEPTOR 2

-

Page/Page column 80, (2021/08/06)

The present application provides a compound of Formula: or a pharmaceutically acceptable salt thereof, wherein ring B, L1, ring A, L2, n, R1, R2, R3, R4, and X1 are as described herein. Pharmaceutical compositions comprising the compound, as well as the methods of making and using the compound, are also provided.

Selective GlyT1 inhibitors: Discovery of [4-(3-fluoro-5- trifluoromethylpyridin-2-yl)piperazin-1-yl][5-methanesulfonyl-2-((S)-2,2, 2-trifluoro-1-methylethoxy)phenyl]methanone (RG1678), a promising novel medicine to treat schizophrenia

Pinard, Emmanuel,Alanine, Alexander,Alberati, Daniela,Bender, Markus,Borroni, Edilio,Bourdeaux, Patrick,Brom, Virginie,Burner, Serge,Fischer, Holger,Hainzl, Dominik,Halm, Remy,Hauser, Nicole,Jolidon, Synese,Lengyel, Judith,Marty, Hans-Peter,Meyer, Thierry,Moreau, Jean-Luc,Mory, Roland,Narquizian, Robert,Nettekoven, Mathias,Norcross, Roger D.,Puellmann, Bernd,Schmid, Philipp,Schmitt, Sebastien,Stalder, Henri,Wermuth, Roger,Wettstein, Joseph G.,Zimmerli, Daniel

experimental part, p. 4603 - 4614 (2010/09/17)

The GlyT1 transporter has emerged as a key novel target for the treatment of schizophrenia. Herein, we report on the optimization of the 2-alkoxy-5-methylsulfonebenzoylpiperazine class of GlyT1 inhibitors to improve hERG channel selectivity and brain penetration. This effort culminated in the discovery of compound 10a (RG1678), the first potent and selective GlyT1 inhibitor to have a beneficial effect in schizophrenic patients in a phase II clinical trial.

Sulfanyl substituted phenyl methanones

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Page/Page column 7, (2008/06/13)

The present invention relates to compounds of formula I wherein R1, R2, R3, X, X1, and n are as defined in the specification and pharmaceutically acceptable acid addition salts thereof. These compounds are good inhibitors of the glycine transporter 1 (GlyT-1) for the treatment CNS disorders, such as schizophrenia, cognitive impairment, and Alzheimer's disease.

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