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FMOC-L-Homophenylalanine is a derivative of the amino acid phenylalanine, featuring an additional FMOC (9-fluorenylmethyloxycarbonyl) protecting group. FMOC-L-HOMOPHENYLALANINE is integral in peptide synthesis, allowing for the incorporation of the amino acid into peptides to investigate the structure and function of proteins. The FMOC group shields the amino acid during the synthesis process and is removed once the peptide assembly is complete. FMOC-L-Homophenylalanine is a promising component in the development of new pharmaceuticals, biotechnology research, and chemical biology studies, with its unique chemical properties and functionality making it a valuable asset in peptide and protein science.

204384-69-0

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204384-69-0 Usage

Uses

Used in Pharmaceutical Development:
FMOC-L-Homophenylalanine is utilized as a building block in the synthesis of peptides for the development of new pharmaceuticals. Its incorporation into peptides aids in the exploration of protein structures and functions, which is crucial for understanding disease mechanisms and designing effective treatments.
Used in Biotechnology Research:
In biotechnology, FMOC-L-Homophenylalanine serves as a key component in the creation of novel bioactive peptides. It is used as a research tool to study protein interactions and develop biotechnological applications, such as the engineering of enzymes or the creation of biosensors.
Used in Chemical Biology Studies:
FMOC-L-Homophenylalanine is employed as a specialized amino acid in chemical biology to probe and manipulate biological systems. It is used as a component in the synthesis of peptides that can modulate biological processes, offering insights into cellular mechanisms and potential therapeutic targets.
Used in Peptide Synthesis:
FMOC-L-Homophenylalanine is used as a protected amino acid in peptide synthesis. The FMOC group protects the amino acid's side chain during the assembly process, ensuring that the peptide sequence is correctly formed without unwanted side reactions. Once the peptide is fully synthesized, the FMOC group is removed, revealing the functional amino acid within the peptide sequence.

Check Digit Verification of cas no

The CAS Registry Mumber 204384-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,3,8 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 204384-69:
(8*2)+(7*0)+(6*4)+(5*3)+(4*8)+(3*4)+(2*6)+(1*9)=120
120 % 10 = 0
So 204384-69-0 is a valid CAS Registry Number.

204384-69-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name FMOC-L-HOMOPHENYLALANINE

1.2 Other means of identification

Product number -
Other names Fmoc-Beta-Homo-Phe-OH

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:204384-69-0 SDS

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