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FMOC-(R)-3-AMINO-3-(1-NAPHTHYL)-PROPIONIC ACID is a chemical compound that is a derivative of 3-amino-3-(1-naphthyl)-propionic acid, featuring a fluorenylmethyloxycarbonyl (FMOC) protecting group. FMOC-(R)-3-AMINO-3-(1-NAPHTHYL)-PROPIONIC ACID is characterized by its (R) stereochemistry, indicating the right-handed enantiomer. It is widely used in the fields of biochemistry and organic chemistry, particularly in peptide synthesis, where the FMOC group serves to temporarily mask the amine group, enabling selective chemical reactions. The unique structure and properties of FMOC-(R)-3-AMINO-3-(1-NAPHTHYL)-PROPIONIC ACID make it a valuable tool in the study and development of pharmaceuticals, as well as in materials science and chemical biology.

511272-47-2

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511272-47-2 Usage

Uses

Used in Peptide Synthesis:
FMOC-(R)-3-AMINO-3-(1-NAPHTHYL)-PROPIONIC ACID is used as a protecting agent in peptide synthesis for the amine group. The FMOC group allows for selective chemical reactions to occur without affecting the amine functionality, which is crucial for the formation of peptide bonds and the synthesis of complex peptide sequences.
Used in Pharmaceutical Development:
In the pharmaceutical industry, FMOC-(R)-3-AMINO-3-(1-NAPHTHYL)-PROPIONIC ACID is used as a building block for the synthesis of various drug candidates. Its unique structure and properties make it a valuable component in the development of new therapeutic agents, particularly those targeting specific biological pathways or receptors.
Used in Materials Science:
FMOC-(R)-3-AMINO-3-(1-NAPHTHYL)-PROPIONIC ACID is utilized in materials science for the development of novel materials with specific properties. Its unique structure and reactivity can be exploited to create materials with tailored characteristics, such as improved stability, selectivity, or biocompatibility.
Used in Chemical Biology:
In the field of chemical biology, FMOC-(R)-3-AMINO-3-(1-NAPHTHYL)-PROPIONIC ACID is used as a tool for studying biological processes and interactions. Its unique structure allows for the investigation of molecular recognition, signaling pathways, and other biological phenomena, contributing to a deeper understanding of biological systems and the development of new therapeutic strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 511272-47-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,1,2,7 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 511272-47:
(8*5)+(7*1)+(6*1)+(5*2)+(4*7)+(3*2)+(2*4)+(1*7)=112
112 % 10 = 2
So 511272-47-2 is a valid CAS Registry Number.

511272-47-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (3R)-3-(9H-fluoren-9-ylmethoxycarbonylamino)-3-naphthalen-1-ylpropanoic acid

1.2 Other means of identification

Product number -
Other names Fmoc-(R)-3-Amino-3-(1-naphthyl)-propionic 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:511272-47-2 SDS

511272-47-2Downstream Products

511272-47-2Relevant academic research and scientific papers

Immunomodulation with novel pharmaceutical compositions

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Page 4; Sheet 19, (2010/02/09)

The synthesis and use of a novel class of tumor necrosis factor (TNFα) inhibitors and immunomodulators are provided. These compounds have pharmacological applications as well as uses in assays relating to TNFα and other involved cytokines. As pharmaceutic

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