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887592-68-9

2-(2-CYANO-ACETYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER is a chemical compound that belongs to the class of piperidine carboxylic acid derivatives. It is a synthetic intermediate used in the pharmaceutical industry for the production of various drugs and active pharmaceutical ingredients. As a tert-butyl ester, it contains a tert-butyl functional group, and the presence of the cyano-acetyl group and piperidine ring in its structure makes it a versatile building block for the synthesis of complex molecules. It is commonly used in the development of drugs for neurological and psychiatric disorders, as well as for pain management. Due to its diverse applications, 2-(2-cyano-acetyl)-piperidine-1-carboxylic acid tert-butyl ester is an important compound in the field of medicinal chemistry and drug discovery.

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  • 887592-68-9 Structure

  • Basic information

    1. Product Name: 2-(2-CYANO-ACETYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
    2. Synonyms: 2-(2-CYANO-ACETYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER;tert-Butyl 2-(2-cyanoacetyl)piperidine-1-carboxylate
    3. CAS NO:887592-68-9
    4. Molecular Formula: C13H20N2O3
    5. Molecular Weight: 252.31
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 887592-68-9.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: 2-(2-CYANO-ACETYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2-CYANO-ACETYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER(887592-68-9)
    11. EPA Substance Registry System: 2-(2-CYANO-ACETYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER(887592-68-9)

  • 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: 887592-68-9(Hazardous Substances Data)

887592-68-9 Usage

Uses

Used in Pharmaceutical Industry:
2-(2-CYANO-ACETYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER is used as a synthetic intermediate for the production of various drugs and active pharmaceutical ingredients.
Used in Drug Development for Neurological and Psychiatric Disorders:
2-(2-CYANO-ACETYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER is used as a building block in the synthesis of complex molecules for the development of drugs targeting neurological and psychiatric disorders.
Used in Pain Management:
2-(2-CYANO-ACETYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER is used in the development of drugs for pain management, leveraging its versatile chemical structure to create effective analgesic compounds.
Used in Medicinal Chemistry and Drug Discovery:
2-(2-CYANO-ACETYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER is utilized as an important compound in the field of medicinal chemistry and drug discovery, contributing to the advancement of new therapeutic agents and treatment options.

Check Digit Verification of cas no

The CAS Registry Mumber 887592-68-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,7,5,9 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 887592-68:
(8*8)+(7*8)+(6*7)+(5*5)+(4*9)+(3*2)+(2*6)+(1*8)=249
249 % 10 = 9
So 887592-68-9 is a valid CAS Registry Number.

887592-68-9SDS

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 2-(2-cyanoacetyl)piperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-Piperidinecarboxylicacid,2-(2-cyanoacetyl)-,1,1-dimethylethyl ester

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:887592-68-9 SDS

887592-68-9Downstream Products

887592-68-9Relevant articles and documents

PIPERIDINE SUBSTITUTED TRICYCLIC PYRAZOLO[1,5-A]PYRIMIDINE DERIVATIVES WITH INHIBITORY ACTIVITY ON THE REPLICATION OF THE RESPIRATORY SYNCYTIAL VIRUS (RSV)

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Page/Page column 16; 17; 18, (2016/06/28)

The invention concerns novel substituted tricyclic pyrazolo pyrimidine compounds of formula (I-a) or (I-b) having antiviral activity, in particular, having an inhibitory activity on the replication of the respiratory syncytial virus (RSV). The invention further concerns the preparation of such novel compounds, compositions comprising these compounds, and the compounds for use in the treatment of respiratory syncytial virus infection.

PIPERIDINE SUBSTITUTED PYRAZOLO[1,5-A]PYRIMIDINE DERIVATIVES WITH INHIBITORY ACTIVITY ON THE REPLICATION OF THE RESPIRATORY SYNCYTIAL VIRUS (RSV)

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Page/Page column 18; 19, (2016/11/07)

The invention concerns novel substituted bicyclic pyrazolo pyrimidine compounds of formula (I) having antiviral activity, in particular, having an inhibitory activity on the replication of the respiratory syncytial virus (RSV). The invention further conce

Discovery of pyrazolo[1,5-a]pyrimidine-based CHK1 inhibitors: A template-based approach - Part 1

Dwyer, Michael P.,Paruch, Kamil,Labroli, Marc,Alvarez, Carmen,Keertikar, Kerry M.,Poker, Cory,Rossman, Randall,Fischmann, Thierry O.,Duca, Jose S.,Madison, Vincent,Parry, David,Davis, Nicole,Seghezzi, Wolfgang,Wiswell, Derek,Guzi, Timothy J.

scheme or table, p. 471 - 474 (2011/02/26)

The synthesis and hit-to-lead SAR development of a pyrazolo[1,5-a] pyrimidine hit 4 is described leading to a series of potent, selective CHK1 inhibitors such as compound 17r. In the Letter, the further utility of the pyrazolo[1,5-a]pyrimidine template fo

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