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Fmoc-(R)-3-Amino-4-(2-naphthyl)-butyric acid is a type of Fmoc-amino acid, a class of chemical compounds extensively used in solid-phase peptide synthesis (SPPS). The Fmoc moiety serves as a protective group for the amino acid, enabling selective reactions during synthesis. This specific compound features a naphthyl group, which may contribute to unique interactions within a peptide sequence due to the π-π (pi-pi) interactions resulting from the conjugated rings. Fmoc-(R)-3-Amino-4-(2-naphthyl)-butyric acid is crucial for the production of peptides, which are vital for a wide array of biological functions.

269398-91-6

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269398-91-6 Usage

Uses

Used in Pharmaceutical Industry:
Fmoc-(R)-3-Amino-4-(2-naphthyl)-butyric acid is used as a building block for the synthesis of peptides and proteins, which are essential for various therapeutic applications. The naphthyl group's unique interactions can potentially enhance the stability, solubility, or biological activity of the resulting peptides.
Used in Research and Development:
In the field of research, Fmoc-(R)-3-Amino-4-(2-naphthyl)-butyric acid is used as a component in the design and synthesis of novel peptides for studying their structure, function, and interactions with other biomolecules. The naphthyl group may provide insights into the role of aromatic interactions in peptide folding and binding.
Used in Diagnostic Applications:
Fmoc-(R)-3-Amino-4-(2-naphthyl)-butyric acid can be incorporated into diagnostic peptides or used as a label in assays to improve the detection and quantification of biological targets. The naphthyl group may enhance the fluorescence or other detection properties of the diagnostic agents.
Used in Material Science:
Fmoc-(R)-3-Amino-4-(2-naphthyl)-butyric acid may be used in the development of novel materials with specific properties, such as self-assembling peptides or peptide-based hydrogels. The naphthyl group could contribute to the formation of supramolecular structures and influence the material's mechanical or optical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 269398-91-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,9,3,9 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 269398-91:
(8*2)+(7*6)+(6*9)+(5*3)+(4*9)+(3*8)+(2*9)+(1*1)=206
206 % 10 = 6
So 269398-91-6 is a valid CAS Registry Number.
InChI:InChI=1/C29H25NO4/c31-28(32)17-22(16-19-13-14-20-7-1-2-8-21(20)15-19)30-29(33)34-18-27-25-11-5-3-9-23(25)24-10-4-6-12-26(24)27/h1-15,22,27H,16-18H2,(H,30,33)(H,31,32)/t22-/m1/s1

269398-91-6SDS

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 FMOC-(R)-3-AMINO-4-(2-NAPHTHYL)-BUTYRIC ACID

1.2 Other means of identification

Product number -
Other names FMOC-(R)-3-AMINO-4-(2-NAPHTHYL)-BUTYRICACID

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:269398-91-6 SDS

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