39621-72-2

Basic information

• Product Name: BOC-GLY-ARG-OH
• Synonyms: BOC-GLY-ARG-OH;N-Boc-Gly-L-Arg-OH;Boc-GR-OH
• CAS NO: 39621-72-2
• Molecular Formula: C13H25N5O5
• Molecular Weight: 331.37
• Mol File: 39621-72-2.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Density: 1.33±0.1 g/cm3(Predicted)
• Storage Temp.: -15°C
• PKA: 3.42±0.10(Predicted)
• CAS DataBase Reference: BOC-GLY-ARG-OH(CAS DataBase Reference)
• NIST Chemistry Reference: BOC-GLY-ARG-OH(39621-72-2)
• EPA Substance Registry System: BOC-GLY-ARG-OH(39621-72-2)

Safety Data

• Hazardous Substances Data: 39621-72-2(Hazardous Substances Data)

Usage

General Description

BOC-GLY-ARG-OH is a chemical compound with the chemical formula C20H38N6O6. It is a peptide derivative, consisting of a BOC (tert-butyloxycarbonyl) protecting group attached to the N-terminal glycine, followed by arginine and a C-terminal hydroxyl group. BOC-GLY-ARG-OH is commonly used in chemical synthesis as a building block for peptides and proteins. It is important in the field of biochemistry and pharmaceutical research due to its ability to mimic and manipulate the structure and function of proteins. BOC-GLY-ARG-OH has potential applications in drug development, particularly in the design of peptide-based therapeutics.

Upstream product

• 4530-20-5 BOC-glycine 
• 24424-99-5 di-tert-butyl dicarbonate 
• 3392-07-2 tert-butyl N-{2-[(2,5-dioxopyrrolidin-1-yl)oxy]-2-oxoethyl}carbamate 
• 74-79-3 L-arginine 

Relevant articles and documents

Amino acid substrate and preparation method and purpose thereof

The invention discloses an amino acid substrate. A structural formula of the substrate is shown in Figure 1. By means of development and innovation of a synthetic process of dipeptide in the amino acid substrate and a coupling process of the dipeptide and chromogen and innovation and application verification of an extraction and purification process, the reaction yield of each step of a product isgreatly improved, the color is close to white, the influence of the substrate color in the identification process is reduced, and the sensitivity and the accuracy of the aerobic flora vaginitis detection process are improved to a greater extent. The substrate is in the form of hydrochloride, and the solubility of the substrate can be greatly improved when the detection is carried out in the formof the hydrochloride. In a detection application, the corresponding preparation work is conducted according to the preparation requirement of the aerobic flora vaginitis detection, and the color rendering performance of the synthetic substrate is compared with the color rendering performance of the existing aerobic flora vaginitis detection in the market according to a detection standard. The color rendering performance is better than that of an aerobic flora vaginitis detection reagent in the market.