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Boc-Cys(Trt)-Pro-OH is a complex compound consisting of three distinct chemical groups: Boc, Cys(Trt), and Pro-OH. The Boc group serves as a protective agent for the amino group of cysteine, averting undesired chemical reactions. The Cys(Trt) group is a cysteine derivative featuring a trityl protecting group, which is a standard in peptide synthesis. The Pro-OH group is a proline derivative with a hydroxyl group, a common component in bioactive peptides and proteins. Boc-Cys(Trt)-Pro-OH is widely utilized in the synthesis of custom peptides and in chemical biology research to explore peptide-protein interactions.

40472-53-5

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40472-53-5 Usage

Uses

Used in Peptide Synthesis:
Boc-Cys(Trt)-Pro-OH is used as a building block for the synthesis of custom peptides, providing a protected cysteine residue that can be selectively deprotected and incorporated into peptide sequences. Its use ensures the prevention of unwanted side reactions during the synthesis process, allowing for the creation of complex peptide structures with specific functionalities.
Used in Chemical Biology Research:
In the field of chemical biology, Boc-Cys(Trt)-Pro-OH is employed as a component in the study of peptide-protein interactions. Its presence in custom peptides allows researchers to investigate the binding specificity, stability, and biological activity of these peptides with their target proteins, contributing to a deeper understanding of molecular recognition and signaling processes.
Used in Pharmaceutical Development:
Boc-Cys(Trt)-Pro-OH is utilized in the development of pharmaceuticals, particularly in the design of peptide-based drugs. Its incorporation into peptide sequences can enhance the stability, bioavailability, and therapeutic efficacy of these drugs, making it a valuable tool in the creation of novel therapeutic agents for various diseases and conditions.
Used in Bioactive Peptide Production:
In the production of bioactive peptides, Boc-Cys(Trt)-Pro-OH is used as a key component to impart specific biological activities to the peptides. Its presence can modulate the peptide's interaction with biological targets, potentially leading to the development of peptides with enhanced health benefits or therapeutic properties.
Used in Cosmetics and Personal Care:
Boc-Cys(Trt)-Pro-OH is also used in the cosmetics and personal care industry, where it can be incorporated into formulations to provide skin-protecting and anti-aging properties. Its presence in cosmetic products can contribute to the development of peptides with improved moisturizing, firming, and rejuvenating effects on the skin.

Check Digit Verification of cas no

The CAS Registry Mumber 40472-53-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,4,7 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 40472-53:
(7*4)+(6*0)+(5*4)+(4*7)+(3*2)+(2*5)+(1*3)=95
95 % 10 = 5
So 40472-53-5 is a valid CAS Registry Number.

40472-53-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-1-[(2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-tritylsulfanylpropanoyl]pyrrolidine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names BOCCys(Trit)ProOH

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:40472-53-5 SDS

40472-53-5Downstream Products

40472-53-5Relevant academic research and scientific papers

USE OF TRIMETHYLSILYL PROTECTION IN THE SYNTHESIS OF OXYTOCIN FRAGMENTS

Ivanov, A. K.,Antonov, A. A.,Donetskii, I. A.

, p. 95 - 97 (2007/10/02)

The possibility has been studied of obtaining silyl derivatives of amino acids forming components of oxytocin and of obtaining the corresponding peptides from them by the mixed-anhydride method.

SYNTHESIS OF THE C-TERMINAL TETRAPEPTIDE OF THE OXYTOCIN SEQUENCE USING VARIOUS PROTECTIVE GROUPS FOR THE CYSTEINE THIOL FUNCTION

Ivanov, A. K.,Grigor'eva, E. E.,Antonov, A. A.,Donetskii, I. A.

, p. 350 - 355 (2007/10/02)

The synthesis of amides of tetrapeptides with the 6-9 sequence of oxytocin containing various protective groups for the thiol function has been performed by 2+2 and 1+3 schemes.Relationships between the yield of tetrapeptide and the structures of the protective groups have been obtained.An advantage of trityl and benzyl protective groups for masking the tiol function of cysteine has been shown.The signals of the 13C NMR spectra of the compounds obtained have been interpreted.

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