2418-95-3 Usage
Description
Ne-Boc-L-lysine, also known as N-(tert-butoxycarbonyl)-L-lysine, is a synthetic derivative of the naturally occurring amino acid L-lysine. It is a white crystalline powder with unique chemical properties that make it valuable in various applications across different industries.
Uses
Used in Pharmaceutical Industry:
Ne-Boc-L-lysine is used as an intermediate in the synthesis of various pharmaceutical compounds for the development of new drugs. Its chemical properties allow for the creation of novel drug candidates with potential therapeutic applications.
Used in Biochemical Research:
In the field of biochemical research, Ne-Boc-L-lysine serves as a valuable reagent for studying protein structure and function. Its unique properties enable researchers to investigate the interactions between proteins and other biomolecules, contributing to a better understanding of biological processes.
Used in Chemical Synthesis:
Ne-Boc-L-lysine is utilized as a building block in the synthesis of complex organic molecules, including peptides and other bioactive compounds. Its versatility as a synthetic intermediate makes it a valuable tool in the development of new chemical entities with potential applications in various industries.
Used in Cosmetics Industry:
In the cosmetics industry, Ne-Boc-L-lysine is used as an ingredient in the formulation of skincare and hair care products. Its properties may contribute to improved skin hydration, hair strength, and overall product performance.
Used in Food Industry:
Ne-Boc-L-lysine may also find applications in the food industry, where it can be used as an additive to enhance the nutritional value of certain products or as a component in the development of novel food ingredients with specific functional properties.
Check Digit Verification of cas no
The CAS Registry Mumber 2418-95-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,1 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2418-95:
(6*2)+(5*4)+(4*1)+(3*8)+(2*9)+(1*5)=83
83 % 10 = 3
So 2418-95-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H22N2O4/c1-11(2,3)17-10(16)8(13)6-4-5-7(12)9(14)15/h7-8H,4-6,12-13H2,1-3H3,(H,14,15)/t7-,8?/m0/s1
2418-95-3Relevant articles and documents
Thermal cleavage of the Fmoc protection group
Hoeck, Stefan,Marti, Roger,Riedl, Rainer,Simeunovic, Marina
experimental part, p. 200 - 202 (2011/08/05)
The Fmoc protection group is among the most commonly used protection groups for the amino function. A fast method for the thermal deavage of this protection group under base-free conditions without the need for dibenzofulvene scavengers is presented. The advantages of this method include straightforward testability by means of a simple high-temperature NMR experiment, usually high yields, and good selectivity towards the BOC protection group and t-butyl ethers.
Dual linker with a reference cleavage site for information rich analysis of polymer-supported transformations
Krchňák, Viktor,Slough, Greg A.
, p. 5237 - 5241 (2007/10/03)
Two dual linker systems with specific reference cleavage sites were designed and synthesized to accelerate and simplify development and optimization of reaction conditions for solid-phase synthesis. The dual linker allows simple evaluation of cleavage rate of polymer-supported compounds from the linker and, at the same time, ensures that all resin-bound components are cleaved from the solid support. The dual linker 4 was assembled from two Wang linkers connected by a three carbon spacer. The linker 9 was synthesized using the PAL and HMPB linkers.
