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Methyl N-Cbz-2-piperidineacetate is a versatile chemical compound and a derivative of piperidine, widely utilized in organic synthesis and pharmaceutical research. It serves as a building block for the development of various pharmaceuticals and fine chemicals, and is particularly known for its role as a protecting group for amines, which aids in facilitating specific reactions in organic synthesis. Methyl N-Cbz-2-piperidineacetate's unique structure and reactivity make it an indispensable tool for chemists in the creation of complex organic molecules with targeted functional groups, thereby playing a significant role in the advancement of organic chemistry and drug development.

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  • 169384-56-9 Structure
  • Basic information

    1. Product Name: Methyl N-Cbz-2-piperidineacetate
    2. Synonyms: Methyl N-Cbz-2-piperidineacetate;Benzyl 2-(2-methoxy-2-oxoethyl)piperidine-1-carboxylate
    3. CAS NO:169384-56-9
    4. Molecular Formula: C16H21NO4
    5. Molecular Weight: 291.34224
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 169384-56-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 402.9±28.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.149±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: -2.52±0.40(Predicted)
    10. CAS DataBase Reference: Methyl N-Cbz-2-piperidineacetate(CAS DataBase Reference)
    11. NIST Chemistry Reference: Methyl N-Cbz-2-piperidineacetate(169384-56-9)
    12. EPA Substance Registry System: Methyl N-Cbz-2-piperidineacetate(169384-56-9)
  • 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: 169384-56-9(Hazardous Substances Data)

169384-56-9 Usage

Uses

Used in Organic Synthesis:
Methyl N-Cbz-2-piperidineacetate is used as a building block for the synthesis of complex organic molecules, due to its ability to act as a protecting group for amines, which facilitates specific reactions and enhances the efficiency of the synthesis process.
Used in Pharmaceutical Research and Development:
In the pharmaceutical industry, Methyl N-Cbz-2-piperidineacetate is used as a key intermediate in the creation of various pharmaceuticals, contributing to the development of new drugs with specific therapeutic properties.
Used in Fine Chemicals Production:
Methyl N-Cbz-2-piperidineacetate is employed in the production of fine chemicals, where its unique reactivity and structure are leveraged to create high-quality specialty chemicals for various applications.
Overall, Methyl N-Cbz-2-piperidineacetate's multifaceted applications across different industries underscore its importance in the fields of organic chemistry, pharmaceutical research, and fine chemicals production, making it a valuable asset for chemists and researchers alike.

Check Digit Verification of cas no

The CAS Registry Mumber 169384-56-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,3,8 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 169384-56:
(8*1)+(7*6)+(6*9)+(5*3)+(4*8)+(3*4)+(2*5)+(1*6)=179
179 % 10 = 9
So 169384-56-9 is a valid CAS Registry Number.

169384-56-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl 2-(2-methoxy-2-oxoethyl)piperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-N-CBZ-2-METHOXYCARBONYLMETHYL-PIPERIDINE

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:169384-56-9 SDS

169384-56-9Relevant articles and documents

Chemoenzymatic approach to enantiopure piperidine-based β-amino esters in organic solvents

Liljeblad, Arto,Kavenius, Hanna-Maija,Taehtinen, Petri,Kanerva, Liisa T.

, p. 181 - 191 (2007/10/03)

This research concentrates on the enantioselectivities of lipase-catalysed reactions with methyl esters of 2-piperidylacetic acid and 3-piperidinecarboxylic acid derivatives. N-Acetylated 2-piperidylacetic acid methyl ester displayed good enantioselectivi

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