What is the Boc-HPh-Leu-Phe-OMe?

Boc-HPh-Leu-Phe-OMe is , while it's Molecular Formula is C31H43N3O6. Used in Peptide Synthesis: Boc-HPh-Leu-Phe-OMe is used as a building block in peptide synthesis for the creation of specific peptide sequences. The Boc protecting group allows for the stepwise addition of amino acids without premature reaction of the amine group, facilitating the controlled synthesis of complex peptide structures. Used in Pharmaceutical Development: In the pharmaceutical industry, Boc-HPh-Leu-Phe-OMe is used as a precursor in the development of peptide-based drugs. Boc-HPh-Leu-Phe-OMe's specific sequence of amino acids can be tailored to target particular biological pathways or receptors, potentially leading to the discovery of new therapeutic agents. Used in Biological Research: Boc-HPh-Leu-Phe-OMe is utilized as a research tool in biological studies to investigate the roles and interactions of specific amino acid sequences within proteins. This can provide insights into protein function, structure, and mechanisms of action, contributing to a deeper understanding of biological processes and disease mechanisms. Used in Drug Delivery Systems: In drug delivery, Boc-HPh-Leu-Phe-OMe can be employed to improve the stability and bioavailability of peptide-based therapeutics. Boc-HPh-Leu-Phe-OMe's protective groups can be strategically removed under specific conditions, allowing for controlled release of the active peptide in the body, enhancing its therapeutic efficacy. Each of these applications leverages the unique properties of Boc-HPh-Leu-Phe-OMe, highlighting its versatility and importance in the fields of chemistry and biology.

What is the CAS number for Boc-HPh-Leu-Phe-OMe?

The CAS number of Boc-HPh-Leu-Phe-OMe is 868539-96-2.

What is Boc-HPh-Leu-Phe-OMe (868539-96-2) used for?

Boc-HPh-Leu-Phe-OMe is a complex chemical compound that features a Boc (tert-butoxycarbonyl) protecting group, followed by the sequence of amino acids phenylalanine, leucine, and phenylalanine, and capped with a methoxy (OMe) group. The Boc group is utilized to shield the amine group of amino acids during peptide synthesis, ensuring the integrity of the molecule during the process. The amino acids leucine and phenylalanine are integral to protein synthesis and are involved in a variety of biological functions. The methoxy group serves as a protective group for the carboxyl group of amino acids, preventing unwanted reactions. Boc-HPh-Leu-Phe-OMe, with its unique structure, holds potential for applications in the fields of peptide synthesis and biological research.

What is the Boc-HPh-Leu-Phe-OMe?

Boc-HPh-Leu-Phe-OMe is , while it's Molecular Formula is C31H43N3O6. Used in Peptide Synthesis: Boc-HPh-Leu-Phe-OMe is used as a building block in peptide synthesis for the creation of specific peptide sequences. The Boc protecting group allows for the stepwise addition of amino acids without premature reaction of the amine group, facilitating the controlled synthesis of complex peptide structures. Used in Pharmaceutical Development: In the pharmaceutical industry, Boc-HPh-Leu-Phe-OMe is used as a precursor in the development of peptide-based drugs. Boc-HPh-Leu-Phe-OMe's specific sequence of amino acids can be tailored to target particular biological pathways or receptors, potentially leading to the discovery of new therapeutic agents. Used in Biological Research: Boc-HPh-Leu-Phe-OMe is utilized as a research tool in biological studies to investigate the roles and interactions of specific amino acid sequences within proteins. This can provide insights into protein function, structure, and mechanisms of action, contributing to a deeper understanding of biological processes and disease mechanisms. Used in Drug Delivery Systems: In drug delivery, Boc-HPh-Leu-Phe-OMe can be employed to improve the stability and bioavailability of peptide-based therapeutics. Boc-HPh-Leu-Phe-OMe's protective groups can be strategically removed under specific conditions, allowing for controlled release of the active peptide in the body, enhancing its therapeutic efficacy. Each of these applications leverages the unique properties of Boc-HPh-Leu-Phe-OMe, highlighting its versatility and importance in the fields of chemistry and biology.

What is the CAS number for Boc-HPh-Leu-Phe-OMe?

The CAS number of Boc-HPh-Leu-Phe-OMe is 868539-96-2.

What is Boc-HPh-Leu-Phe-OMe (868539-96-2) used for?

Boc-HPh-Leu-Phe-OMe is a complex chemical compound that features a Boc (tert-butoxycarbonyl) protecting group, followed by the sequence of amino acids phenylalanine, leucine, and phenylalanine, and capped with a methoxy (OMe) group. The Boc group is utilized to shield the amine group of amino acids during peptide synthesis, ensuring the integrity of the molecule during the process. The amino acids leucine and phenylalanine are integral to protein synthesis and are involved in a variety of biological functions. The methoxy group serves as a protective group for the carboxyl group of amino acids, preventing unwanted reactions. Boc-HPh-Leu-Phe-OMe, with its unique structure, holds potential for applications in the fields of peptide synthesis and biological research.

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868539-96-2

Product Name:Boc-HPh-Leu-Phe-OMe
Molecular Formula:C31H43N3O6
Molecular Weight:553.699

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Product Details

Purity:99%

High Quality Chinese Factory supply 868539-96-2 Boc-HPh-Leu-Phe-OMe

Molecular Formula:C31H43N3O6
Molecular Weight:553.699
Boiling Point:753.4±60.0 °C(Predicted)
PKA:11.22±0.46(Predicted)
PSA：122.83000
Density:1.123±0.06 g/cm3(Predicted)
LogP:5.11660

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868539-96-2 Process route

: 82732-07-8,108524-68-1,142926-43-0,100564-78-1
Boc-L-homophenylalanine

: Leu-Phe-OMe trifluoroacetate

: 868539-96-2
(S)-methyl 2-((S)-2-tert.butoxycarbonyIamino-4-phenylbutanamido-4-methylpentanamido)-3-phenylpropanoate

Conditions

Conditions	Yield
With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine; In DMF (N,N-dimethyl-formamide); at 0 - 20 ℃;
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 20 ℃; for 12h;

: 15136-32-0,87976-66-7,120342-25-8,5874-73-7
(N-(tert-butoxycarbonyl)-L-leucinyl)-L-phenylalanine methyl ester

: 82732-07-8,108524-68-1,142926-43-0,100564-78-1
Boc-L-homophenylalanine

: 868539-96-2
(S)-methyl 2-((S)-2-tert.butoxycarbonyIamino-4-phenylbutanamido-4-methylpentanamido)-3-phenylpropanoate

Conditions

Conditions	Yield
(N-(tert-butoxycarbonyl)-L-leucinyl)-L-phenylalanine methyl ester; With trifluoroacetic acid; In dichloromethane; at 0 - 20 ℃; for 2h; Boc-L-homophenylalanine; With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide; at 0 - 20 ℃; Inert atmosphere;	21.59 g
(N-(tert-butoxycarbonyl)-L-leucinyl)-L-phenylalanine methyl ester; With trifluoroacetic acid; In dichloromethane; Boc-L-homophenylalanine; With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane;	246 mg

868539-96-2 Upstream products

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L-leucyl-L-phenylalanine methyl ester
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868539-96-2 Downstream products

868539-99-5
C₂HF₃O₂*C₂₆H₃₅N₃O₄
868540-08-3
C₂₈H₃₆ClN₃O₅
1140908-89-9
C₃₂H₄₄N₄O₆
868540-16-3
(S)-2-((S)-4-methyl-2-((S)-2-(2-morpholinoacetamido)-4-phenylbutanamido)pentanamido)-3-phenyipropanoic acid

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