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(S)-(1-FMOC-PIPERIDIN-2-YL)-ACETIC ACID is a chiral compound derived from piperidine and acetic acid, featuring a specific stereochemical configuration denoted by the (S) prefix. (S)-(1-FMOC-PIPERIDIN-2-YL)-ACETIC ACID is characterized by its Fmoc (Fluorenylmethyloxycarbonyl) protecting group and a piperidine ring structure, which contribute to its utility in organic synthesis and pharmaceutical research. (S)-(1-FMOC-PIPERIDIN-2-YL)-ACETIC ACID's unique properties allow it to modify and enhance the characteristics of other molecules, making it a valuable asset in the development of new drugs and materials.

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  • 193693-62-8 Structure
  • Basic information

    1. Product Name: (S)-(1-FMOC-PIPERIDIN-2-YL)-ACETIC ACID
    2. Synonyms: (S)-(1-FMOC-PIPERIDIN-2-YL)-ACETIC ACID;(S)-FMOC-(2-CARBOXYMETHYL)-PIPERIDINE;(S)-2-(1-(((9H-Fluoren-9-yl)methoxy)carbonyl)piperidin-2-yl)acetic acid;2-Piperidineaceticacid, 1-[(9H-fluoren-9-ylmethoxy)carbonyl]-, (2S)-
    3. CAS NO:193693-62-8
    4. Molecular Formula: C22H23NO4
    5. Molecular Weight: 365.42
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 193693-62-8.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.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: (S)-(1-FMOC-PIPERIDIN-2-YL)-ACETIC ACID(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-(1-FMOC-PIPERIDIN-2-YL)-ACETIC ACID(193693-62-8)
    11. EPA Substance Registry System: (S)-(1-FMOC-PIPERIDIN-2-YL)-ACETIC ACID(193693-62-8)
  • 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: 193693-62-8(Hazardous Substances Data)

193693-62-8 Usage

Uses

Used in Pharmaceutical Research and Development:
(S)-(1-FMOC-PIPERIDIN-2-YL)-ACETIC ACID is used as a building block in the synthesis of pharmaceutical compounds due to its ability to modify and enhance the properties of other molecules. Its chiral nature and specific stereochemistry make it a versatile component in the creation of novel drug candidates.
Used in Peptide Synthesis:
In the field of peptide synthesis, (S)-(1-FMOC-PIPERIDIN-2-YL)-ACETIC ACID serves as a crucial component, taking advantage of its Fmoc protecting group. This group is instrumental in the stepwise assembly of peptide chains, protecting the amino acid from unwanted side reactions during the synthesis process.
Used in Organic Synthesis:
(S)-(1-FMOC-PIPERIDIN-2-YL)-ACETIC ACID is utilized as a reagent or intermediate in various organic synthesis processes. Its unique structure and functional groups enable the creation of a wide range of organic compounds for use in different industries, including specialty chemicals and materials science.
Used in Drug Discovery:
(S)-(1-FMOC-PIPERIDIN-2-YL)-ACETIC ACID's potential pharmacological activity, stemming from its piperidine ring structure, positions (S)-(1-FMOC-PIPERIDIN-2-YL)-ACETIC ACID as a valuable tool in drug discovery. Researchers can use (S)-(1-FMOC-PIPERIDIN-2-YL)-ACETIC ACID to explore new therapeutic agents, particularly those targeting the central nervous system or other biological pathways where piperidine-based structures have demonstrated efficacy.
Used in the Development of New Materials:
Beyond its applications in pharmaceuticals, (S)-(1-FMOC-PIPERIDIN-2-YL)-ACETIC ACID also finds use in the development of new materials with unique properties. Its ability to interact with and modify other molecules can lead to the creation of advanced materials for use in various industries, such as coatings, adhesives, or even in the development of new polymers with specialized characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 193693-62-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,6,9 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 193693-62:
(8*1)+(7*9)+(6*3)+(5*6)+(4*9)+(3*3)+(2*6)+(1*2)=178
178 % 10 = 8
So 193693-62-8 is a valid CAS Registry Number.

193693-62-8SDS

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 2-[(2S)-1-(9H-fluoren-9-ylmethoxycarbonyl)piperidin-2-yl]acetic acid

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:193693-62-8 SDS

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