16944-17-5

Usage

Uses

Used in Organic Synthesis:
BOC-VAL-OH DCHA is used as an intermediate in organic synthesis for the preparation of peptides and other biologically active molecules. Its presence of a BOC protecting group and a hydroxyl functional group allows for selective reactions and the formation of complex molecular structures.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, BOC-VAL-OH DCHA is utilized for the production of various drugs and bioactive compounds. Its unique structure and functional groups enable the development of new therapeutic agents with specific biological activities.
Used in Biotechnology Industry:
BOC-VAL-OH DCHA is also employed in the biotechnology industry, where it contributes to the synthesis of bioactive compounds for research and commercial applications. Its role in creating molecules with specific biological functions makes it an essential component in the advancement of biotechnological products.

InChI:InChI=1/C12H23N.C10H19NO4/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12;1-6(2)7(8(12)13)11-9(14)15-10(3,4)5/h11-13H,1-10H2;6-7H,1-5H3,(H,11,14)(H,12,13)

Upstream product

• 72-18-4 L-valine 
• 101-83-7 N-cyclohexyl-cyclohexanamine 
• 13734-41-3 t-Boc-L-valine 
• 24424-99-5 di-tert-butyl dicarbonate 

Downstream Products

• 58872-04-1 Boc-Val-Pro-Pro-OBzl 
• 103725-82-2 Boc-Val-Val-Pro-Pro-OBzl 
• 103725-84-4 Boc-Val-Val-Val-Pro-Pro-OBzl 
• 13734-41-3 t-Boc-L-valine 
• 103725-93-5 Boc-Val-Val-Val-Pro-Pro-Phe-Leu-OBzl 
• 103725-91-3 Boc-Val-Val-Val-Pro-Pro-Phe-Leu-Gln-Pro-OBzl 

Relevant academic research and scientific papers

Gel sculpture: Moldable, load-bearing and self-healing non-polymeric supramolecular gel derived from a simple organic salt

An easy access to a library of simple organic salts derived from tert-butoxycarbonyl (Boc)-protected L-amino acids and two secondary amines (dicyclohexyl- and dibenzyl amine) are synthesized following a supramolecular synthon rationale to generate a new series of low molecular weight gelators (LMWGs). Out of the 12 salts that we prepared, the nitrobenzene gel of dicyclohexylammonium Boc-glycinate (GLY.1) displayed remarkable load-bearing, moldable and self-healing properties. These remarkable properties displayed by GLY.1 and the inability to display such properties by its dibenzylammonium counterpart (GLY.2) were explained using microscopic and rheological data. Single crystal structures of eight salts displayed the presence of a 1D hydrogen-bonded network (HBN) that is believed to be important in gelation. Powder X-ray diffraction in combination with the single crystal X-ray structure of GLY.1 clearly established the presence of a 1D hydrogen-bonded network in the xerogel of the nitrobenzene gel of GLY.1. The fact that such remarkable properties arising from an easily accessible (salt formation) small molecule are due to supramolecular (non-covalent) interactions is quite intriguing and such easily synthesizable materials may be useful in stress-bearing and other applications. Copyright