88224-05-9 Usage
Uses
Used in Chemical Reactions:
L-Isoleucine allyl ester p-toluenesulfonate salt is used as a reactant or catalyst in various chemical reactions, contributing to the synthesis of different compounds and facilitating specific reaction pathways.
Used in Biochemistry Research:
L-Isoleucine allyl ester p-toluenesulfonate salt is employed in biochemistry research to study the interactions and roles of amino acid derivatives in biological systems, potentially leading to advancements in understanding metabolic processes and enzyme mechanisms.
Used in Pharmaceutical Research:
L-Isoleucine allyl ester p-toluenesulfonate salt is used in pharmaceutical research to explore its potential as a therapeutic agent or as a component in the development of new drugs, given its unique structure and properties.
Used in Laboratory Settings:
L-Isoleucine allyl ester p-toluenesulfonate salt is used in laboratory settings for educational purposes, allowing students and researchers to understand the synthesis and properties of amino acid derivatives, as well as their applications in various fields.
Note: Due to the limited information provided on the toxicity and safety measures of L-Isoleucine allyl ester p-toluenesulfonate salt, it is essential to handle L-Isoleucine allyl ester p-toluenesulfonate salt with standard laboratory precautions to ensure safety.
Check Digit Verification of cas no
The CAS Registry Mumber 88224-05-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,2 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 88224-05:
(7*8)+(6*8)+(5*2)+(4*2)+(3*4)+(2*0)+(1*5)=139
139 % 10 = 9
So 88224-05-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H17NO2.C7H8O3S/c1-4-6-12-9(11)8(10)7(3)5-2;1-6-2-4-7(5-3-6)11(8,9)10/h4,7-8H,1,5-6,10H2,2-3H3;2-5H,1H3,(H,8,9,10)/t7-,8-;/m0./s1
88224-05-9Relevant academic research and scientific papers
Allyl Esters as Selectively Removable Carboxy-protecting Functions in Peptide and N-Glycopeptide Syntheses
Waldmann, Herbert,Kunz, Horst
, p. 1712 - 1725 (2007/10/02)
Allyl esters are advantageous in protection of the carboxylic function in peptide and glycopeptide syntheses and can easily be synthesized from amino acids.They are stable under acidic conditions used for the removal of the Boc and Z groups.Under neutral or weakly basic conditions allyl esters are cleaved smoothly on treatment with catalytic amounts of tris(triphenylphosphane)rhodium(I) chloride in ethanol/water (9:1) leaving the N-protecting function and the N-glycosidic bond untouched.Selective deblocking of the α-carboxylic function of protected N-glycosylated asparagine derivatives 15 carried out in this way is exploited in C-terminal chain extension in the synthesis of N-glycotripeptides 17,e.g 17c, the latter representing a partial sequence of a human immunoglobulin G1.
