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2-[1-(TERT-BUTOXYCARBONYL)-4-PIPERIDINYL]-1,3-THIAZOLE-4-CARBOXYLIC ACID is a complex organic compound featuring a piperidine ring connected to a thiazole ring, with a carboxylic acid group attached. The presence of the tert-butoxycarbonyl (Boc) group acts as a protective agent for the nitrogen atom in the piperidine ring, which can be selectively removed to expose the free amine. 2-[1-(TERT-BUTOXYCARBONYL)-4-PIPERIDINYL]-1,3-THIAZOLE-4-CARBOXYLIC ACID holds promise in medicinal chemistry, particularly for the development of pharmaceuticals that target specific biological pathways. Its distinctive structural features and functional groups also make it a valuable component in the synthesis of more intricate molecules with a range of biological activities. Further investigation into its chemical properties and biological effects is essential to uncover its full potential in the realm of drug discovery and development.

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  • 2-[1-(tert-Butoxycarbonyl)-4-piperidinyl]-1,3-thiazole-4-carboxylic acid

    Cas No: 668484-45-5

  • USD $ 1.9-2.9 / Gram

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  • 668484-45-5 Structure
  • Basic information

    1. Product Name: 2-[1-(TERT-BUTOXYCARBONYL)-4-PIPERIDINYL]-1,3-THIAZOLE-4-CARBOXYLIC ACID
    2. Synonyms: 2-(PIPERDIN-4-YL)-1,3-THIAZOLE-4-CARBOXYLIC ACID, N1-BOC PROTECTED;2-[1-(TERT-BUTOXYCARBONYL)PIPERDIN-4-YL]-1,3-THIAZOLE-4-CARBOXYLIC ACID;2-[1-(TERT-BUTOXYCARBONYL)-4-PIPERIDINYL]-1,3-THIAZOLE-4-CARBOXYLIC ACID;2-[1-(tert-butoxycarbonyl)piperid-4-yl]-1,3-thiazole-4-carboxylic acid;2-[1-(tert-butoxycarbonyl)piperidin-4-yl]-1,3-thiazole-4-carboxylic acid;1-(tert-Butoxycarbonyl)-4-(4-carboxy-1,3-thiazol-2-yl)piperidine, 2-[1-(tert-Butoxycarbonyl)piperidin-4-yl]-4-carboxy-1,3-thiazole
    3. CAS NO:668484-45-5
    4. Molecular Formula: C14H20N2O4S
    5. Molecular Weight: 312.38
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 668484-45-5.mol
  • Chemical Properties

    1. Melting Point: 162 °C
    2. Boiling Point: 0°C
    3. Flash Point: 0°C
    4. Appearance: /
    5. Density: 1.279g/cm3
    6. Vapor Pressure: 1.04E-09mmHg at 25°C
    7. Refractive Index: 1.563
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. PKA: 1.35±0.10(Predicted)
    11. CAS DataBase Reference: 2-[1-(TERT-BUTOXYCARBONYL)-4-PIPERIDINYL]-1,3-THIAZOLE-4-CARBOXYLIC ACID(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2-[1-(TERT-BUTOXYCARBONYL)-4-PIPERIDINYL]-1,3-THIAZOLE-4-CARBOXYLIC ACID(668484-45-5)
    13. EPA Substance Registry System: 2-[1-(TERT-BUTOXYCARBONYL)-4-PIPERIDINYL]-1,3-THIAZOLE-4-CARBOXYLIC ACID(668484-45-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: 36/37/38
    3. Safety Statements: 26-36
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 668484-45-5(Hazardous Substances Data)

668484-45-5 Usage

Uses

Used in Medicinal Chemistry:
2-[1-(TERT-BUTOXYCARBONYL)-4-PIPERIDINYL]-1,3-THIAZOLE-4-CARBOXYLIC ACID is used as a key intermediate in the synthesis of pharmaceuticals for targeting specific biological pathways. Its unique structure allows for the creation of molecules with potential therapeutic effects.
Used in Drug Discovery and Development:
In the pharmaceutical industry, 2-[1-(TERT-BUTOXYCARBONYL)-4-PIPERIDINYL]-1,3-THIAZOLE-4-CARBOXYLIC ACID is utilized as a building block for the development of new drugs. Its versatility in chemical synthesis and potential for biological activity make it a valuable asset in the creation of novel therapeutic agents.
Used in Chemical Synthesis:
2-[1-(TERT-BUTOXYCARBONYL)-4-PIPERIDINYL]-1,3-THIAZOLE-4-CARBOXYLIC ACID is used as a synthetic precursor in the preparation of more complex organic molecules. Its functional groups facilitate various chemical reactions, contributing to the synthesis of a diverse range of compounds with potential applications in different fields.
Used in Research and Exploration:
In the field of scientific research, 2-[1-(TERT-BUTOXYCARBONYL)-4-PIPERIDINYL]-1,3-THIAZOLE-4-CARBOXYLIC ACID is employed as a subject of study to explore its chemical reactivity and biological properties. Understanding its behavior in different conditions can lead to the discovery of new applications and insights into its role in drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 668484-45-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,8,4,8 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 668484-45:
(8*6)+(7*6)+(6*8)+(5*4)+(4*8)+(3*4)+(2*4)+(1*5)=215
215 % 10 = 5
So 668484-45-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H20N2O4S/c1-14(2,3)20-13(19)16-6-4-9(5-7-16)11-15-10(8-21-11)12(17)18/h8-9H,4-7H2,1-3H3,(H,17,18)

668484-45-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[1-(TERT-BUTOXYCARBONYL)-4-PIPERIDINYL]-1,3-THIAZOLE-4-CARBOXYLIC ACID

1.2 Other means of identification

Product number -
Other names 2-[1-(tert-butoxycarbonyl)piperid-4-yl]-1,3-thiazole-4-carboxylic acid

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:668484-45-5 SDS

668484-45-5Downstream Products

668484-45-5Relevant articles and documents

SELECTIVE HDAC1,2 INHIBITORS

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Paragraph 0599; 0602; 0603, (2018/06/04)

Provided herein are compounds, pharmaceutical compositions comprising such compounds, and methods of using such compounds to treat diseases or disorders associated with HDAC1 and/or HDAC2 activity.

IMIDAZO[4,5-C]PYRIDINE AND PYRROLO[2,3-C]PYRIDINE DERIVATIVES AS SSAO INHIBITORS

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Page/Page column 40; 41, (2014/09/29)

The compounds of formula (I) are inhibitors of semicarbazide- sensitive amine oxidase (SSAO) activity useful in the treatment of inflammation, an inflammatory disease, an immune or an autoimmune disorder, or inhibition of tumour growth.

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