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(S)-3-Cyclopentyl-3-(9H-fluoren-9-ylmethoxycarbonylamino)-propionic acid, also known by its chemical abbreviation Fmoc-CPP, is a chemical compound that features a cyclopentyl group and a fluorenyl group. (S)-3-CYCLOPENTYL-3-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-PROPIONIC ACID is characterized by its ability to act as a protecting group for amines, which is crucial in the stepwise synthesis of peptide chains. The presence of the fluorenyl group also enhances the solubility of the compound in organic solvents, making it a valuable asset in peptide synthesis reactions. As a result, Fmoc-CPP holds significant importance in the realm of peptide chemistry and organic synthesis.

954225-72-0

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954225-72-0 Usage

Uses

Used in Pharmaceutical Industry:
(S)-3-Cyclopentyl-3-(9H-fluoren-9-ylmethoxycarbonylamino)-propionic acid is used as a protecting group for amines in the pharmaceutical industry for the synthesis of peptides. Its role in solid-phase peptide synthesis method allows for the stepwise construction of peptide chains, which is essential for creating various peptide-based drugs and therapeutics.
Used in Chemical Research:
In the field of chemical research, (S)-3-cyclopentyl-3-(9H-fluoren-9-ylmethoxycarbonylamino)-propionic acid is utilized as a key reagent for peptide chemistry and organic synthesis. Its unique properties, such as the ability to protect amines and enhance solubility in organic solvents, make it a valuable tool for researchers working on the development of new compounds and methodologies.
Used in Peptide Synthesis:
(S)-3-Cyclopentyl-3-(9H-fluoren-9-ylmethoxycarbonylamino)-propionic acid is used as a protecting group for amines in peptide synthesis. This application is crucial for the successful construction of complex peptide structures, which are vital components in various biological and pharmaceutical applications.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-3-cyclopentyl-3-(9H-fluoren-9-ylmethoxycarbonylamino)-propionic acid is employed as a reagent to facilitate the synthesis of various organic compounds. Its ability to enhance solubility in organic solvents and act as a protecting group for amines makes it a versatile and essential component in the development of new synthetic pathways and methodologies.

Check Digit Verification of cas no

The CAS Registry Mumber 954225-72-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,4,2,2 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 954225-72:
(8*9)+(7*5)+(6*4)+(5*2)+(4*2)+(3*5)+(2*7)+(1*2)=180
180 % 10 = 0
So 954225-72-0 is a valid CAS Registry Number.

954225-72-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S)-3-cyclopentyl-3-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid

1.2 Other means of identification

Product number -
Other names (S)-3-cyclopentyl-3-(9H-fluoren-9-ylmethoxycarbonylamino)-propanoic 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:954225-72-0 SDS

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