What is the FMOC-PRO-PRO-PRO-OH?

FMOC-PRO-PRO-PRO-OH is , while it's Molecular Formula is C30H33N3O6. Used in Peptide Synthesis: FMOC-PRO-PRO-PRO-OH is utilized as a building block in the synthesis of peptides, particularly in solid-phase peptide synthesis. Its role is to extend the peptide chain, providing a foundation for the creation of more complex and biologically active molecules. Used in Pharmaceutical Research: In the pharmaceutical industry, FMOC-PRO-PRO-PRO-OH is employed as a precursor in the development of new drugs. Its conformational properties and the presence of proline residues may contribute to the compound's potential therapeutic effects, making it a valuable asset in the discovery and design of novel pharmaceutical agents. Used in Chemical Research: FMOC-PRO-PRO-PRO-OH is also used in chemical research as a model compound to study the properties of peptides and their interactions with other molecules. This can lead to a better understanding of peptide behavior and the development of new chemical methodologies. Used in Biochemical Studies: In biochemical research, FMOC-PRO-PRO-PRO-OH serves as a tool to investigate the mechanisms of peptide folding, stability, and interactions with biological targets. Its use can provide insights into protein structure and function, which are essential for understanding various biological processes and diseases.

What is the CAS number for FMOC-PRO-PRO-PRO-OH?

The CAS number of FMOC-PRO-PRO-PRO-OH is 134303-96-1.

What is FMOC-PRO-PRO-PRO-OH (134303-96-1) used for?

FMOC-PRO-PRO-PRO-OH is a chemical compound composed of three proline amino acids linked by peptide bonds and featuring a 9-fluorenylmethyloxycarbonyl (FMOC) protecting group. FMOC-PRO-PRO-PRO-OH is integral to peptide synthesis and solid-phase peptide synthesis, serving as a fundamental building block for the assembly of longer peptide chains. The FMOC group is removable with an appropriate reagent, facilitating the extension of the peptide or its application in a variety of biological and chemical research contexts. The presence of proline residues in its structure imparts unique conformational characteristics and potential biological functions, making FMOC-PRO-PRO-PRO-OH a crucial component in the fields of peptide chemistry and drug development.

What is the FMOC-PRO-PRO-PRO-OH?

FMOC-PRO-PRO-PRO-OH is , while it's Molecular Formula is C30H33N3O6. Used in Peptide Synthesis: FMOC-PRO-PRO-PRO-OH is utilized as a building block in the synthesis of peptides, particularly in solid-phase peptide synthesis. Its role is to extend the peptide chain, providing a foundation for the creation of more complex and biologically active molecules. Used in Pharmaceutical Research: In the pharmaceutical industry, FMOC-PRO-PRO-PRO-OH is employed as a precursor in the development of new drugs. Its conformational properties and the presence of proline residues may contribute to the compound's potential therapeutic effects, making it a valuable asset in the discovery and design of novel pharmaceutical agents. Used in Chemical Research: FMOC-PRO-PRO-PRO-OH is also used in chemical research as a model compound to study the properties of peptides and their interactions with other molecules. This can lead to a better understanding of peptide behavior and the development of new chemical methodologies. Used in Biochemical Studies: In biochemical research, FMOC-PRO-PRO-PRO-OH serves as a tool to investigate the mechanisms of peptide folding, stability, and interactions with biological targets. Its use can provide insights into protein structure and function, which are essential for understanding various biological processes and diseases.

What is the CAS number for FMOC-PRO-PRO-PRO-OH?

The CAS number of FMOC-PRO-PRO-PRO-OH is 134303-96-1.

What is FMOC-PRO-PRO-PRO-OH (134303-96-1) used for?

FMOC-PRO-PRO-PRO-OH is a chemical compound composed of three proline amino acids linked by peptide bonds and featuring a 9-fluorenylmethyloxycarbonyl (FMOC) protecting group. FMOC-PRO-PRO-PRO-OH is integral to peptide synthesis and solid-phase peptide synthesis, serving as a fundamental building block for the assembly of longer peptide chains. The FMOC group is removable with an appropriate reagent, facilitating the extension of the peptide or its application in a variety of biological and chemical research contexts. The presence of proline residues in its structure imparts unique conformational characteristics and potential biological functions, making FMOC-PRO-PRO-PRO-OH a crucial component in the fields of peptide chemistry and drug development.

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134303-96-1

Product Name：Fmoc-Pro-Pro-Pro-OH
Molecular Formula：C30H33N3O6
Purity：99%
Molecular Weight：531.6

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Product Details;

CasNo： 134303-96-1

Molecular Formula： C30H33N3O6

Factory supply Fmoc-Pro-Pro-Pro-OH 134303-96-1 with sufficient stock and high standard

Molecular Formula:C30H33N3O6
Molecular Weight:531.6
PSA：107.46000
LogP:3.28020

134303-96-1 Relevant articles

Hybrid bombesin analogues: Combining an agonist and an antagonist in defined distances for optimized tumor targeting

Kroll, Carsten,Mansi, Rosalba,Braun, Friederike,Dobitz, Stefanie,Maecke, Helmut R.,Wennemers, Helma

, p. 16793 - 16796 (2013)

Radiolabeled hybrid ligands with defined...

An improved preparation of a tertiary alcohol proline linker and its use in a synthesis of mosquito oostatic hormone

Kochansky,Wagner

, p. 8007 - 8010 (2007/10/02)

An improved synthesis of 4-(3'-hydroxy-3...

134303-96-1 Process route

: 28920-43-6
(fluorenylmethoxy)carbonyl chloride

: 1392411-97-0
H-(Pro)3-OH*TFA salt

: 134303-96-1
Fmoc-Pro-Pro-Pro-OH

Conditions

Conditions	Yield
With sodium hydrogencarbonate;	58%

: Fmoc-Pro-Pro-Pro-O-t-Bu

: 134303-96-1
Fmoc-Pro-Pro-Pro-OH

Conditions

Conditions	Yield
With trifluoroacetic acid;

134303-96-1 Upstream products

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28920-43-6
(fluorenylmethoxy)carbonyl chloride
1392411-97-0
H-(Pro)3-OH*TFA salt

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