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103321-50-2

FMOC-ALA-CL, a chemical compound, is composed of the FMOC (9-fluorenylmethoxycarbonyl) protecting group attached to the amino acid alanine (ALA) via a chloromethyl (CL) linker. It serves as a crucial component in peptide synthesis, providing protection to the amino group of the alanine residue. The FMOC group can be selectively removed under mild acidic conditions, facilitating the deprotection process for subsequent peptide chain elongation. FMOC-ALA-CL is an essential building block in peptide creation and is widely used in chemical research and drug development.

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  • 103321-50-2 Structure

  • Basic information

    1. Product Name: FMOC-ALA-CL
    2. Synonyms: FMOC-L-ALANYL CHLORIDE;FMOC-ALA-CL;NALPHA-9-fluorenylmethoxycarbonyl-L-alanyl chloride;N-[(1S)-1-(Chlorocarbonyl)ethyl]carbamic acid 9H-fluoren-9-ylmethyl ester;Fmoc-L-Phe-Cl;Fmoc-L-Ala-Cl;Fmoc-Beta -Ala-Cl;(S)-(9H-Fluoren-9-yl)methyl(1-chloro-1-oxopropan-2-yl)carbamate
    3. CAS NO:103321-50-2
    4. Molecular Formula: C18H16ClNO3
    5. Molecular Weight: 329.78
    6. EINECS: 1533716-785-6
    7. Product Categories: Amino Acids
    8. Mol File: 103321-50-2.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: FMOC-ALA-CL(CAS DataBase Reference)
    10. NIST Chemistry Reference: FMOC-ALA-CL(103321-50-2)
    11. EPA Substance Registry System: FMOC-ALA-CL(103321-50-2)

  • 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: 103321-50-2(Hazardous Substances Data)

103321-50-2 Usage

Uses

Used in Peptide Synthesis:
FMOC-ALA-CL is used as a protecting agent for the amino group of alanine in peptide synthesis. Its role is to prevent unwanted side reactions during the synthesis process, ensuring the correct formation of peptide bonds.
Used in Chemical Research:
FMOC-ALA-CL is utilized as a key building block in the creation of peptides for various chemical research applications. Its ability to protect the amino group of alanine allows for the controlled synthesis of complex peptide structures.
Used in Drug Development:
In the pharmaceutical industry, FMOC-ALA-CL is employed as a component in the synthesis of bioactive peptides and peptidomimetics. Its selective deprotection capability enables the development of novel therapeutic agents with specific biological activities.
Used in Organic Synthesis:
FMOC-ALA-CL is also used in organic synthesis as a versatile intermediate for the preparation of various organic compounds. Its reactivity and functional groups make it a valuable precursor in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 103321-50-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,3,2 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 103321-50:
(8*1)+(7*0)+(6*3)+(5*3)+(4*2)+(3*1)+(2*5)+(1*0)=62
62 % 10 = 2
So 103321-50-2 is a valid CAS Registry Number.

103321-50-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 9H-fluoren-9-ylmethyl N-[(2S)-1-chloro-1-oxopropan-2-yl]carbamate

1.2 Other means of identification

Product number -
Other names Fmoc-Ala-Cl

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:103321-50-2 SDS

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