34235-82-0 Usage
Uses
Used in Biochemical Research:
NEPSILON-CARBOBENZOXY-NALPHA-TOSYL-L-LYSINE is used as a research tool for studying cellular processes and enzyme activity, particularly focusing on the role of proteases in these mechanisms.
Used in Enzyme Purification and Isolation:
In the field of biochemistry, NEPSILON-CARBOBENZOXY-NALPHA-TOSYL-L-LYSINE serves as a crucial agent in the purification and isolation of enzymes, aiding in the detailed analysis of their structures and functions.
Used in Pharmaceutical Development:
NEPSILON-CARBOBENZOXY-NALPHA-TOSYL-L-LYSINE is employed in the development of pharmaceuticals, potentially contributing to the creation of new drugs that target protease enzymes implicated in various diseases.
Used in Cancer Treatment Research:
NEPSILON-CARBOBENZOXY-NALPHA-TOSYL-L-LYSINE is used as a potential therapeutic agent in cancer treatment studies, exploring its capacity to inhibit proteases that may be involved in tumor growth and progression.
Used in Therapy for Inflammatory Diseases:
NEPSILON-CARBOBENZOXY-NALPHA-TOSYL-L-LYSINE is also being studied for its potential as a therapy for certain inflammatory diseases, where protease inhibition could help modulate the disease process and alleviate symptoms.
Check Digit Verification of cas no
The CAS Registry Mumber 34235-82-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,2,3 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 34235-82:
(7*3)+(6*4)+(5*2)+(4*3)+(3*5)+(2*8)+(1*2)=100
100 % 10 = 0
So 34235-82-0 is a valid CAS Registry Number.
InChI:InChI=1/C21H26N2O6S/c1-16-10-12-18(13-11-16)30(27,28)23-19(20(24)25)9-5-6-14-22-21(26)29-15-17-7-3-2-4-8-17/h2-4,7-8,10-13,19,23H,5-6,9,14-15H2,1H3,(H,22,26)(H,24,25)/t19-/m0/s1
34235-82-0Relevant academic research and scientific papers
Nitrile Synthesis by Aerobic Oxidation of Primary Amines and in situ Generated Imines from Aldehydes and Ammonium Salt with Grubbs Catalyst
Utsumi, Tatsuki,Noda, Kenta,Kawauchi, Daichi,Ueda, Hirofumi,Tokuyama, Hidetoshi
, p. 3583 - 3588 (2020/08/05)
Herein, a Grubbs-catalyzed route for the synthesis of nitriles via the aerobic oxidation of primary amines is reported. This reaction accommodates a variety of substrates, including simple primary amines, sterically hindered β,β-disubstituted amines, allylamine, benzylamines, and α-amino esters. Reaction compatibility with various functionalities is also noted, particularly with alkenes, alkynes, halogens, esters, silyl ethers, and free hydroxyl groups. The nitriles were also synthesized via the oxidation of imines generated from aldehydes and NH4OAc in situ. (Figure presented.).
Highly enantioselective hydrogenation of exocyclic double bond of N-tosyloxazolidinones catalyzed by a neutral rhodium complex and its synthetic applications
Shen, Zengming,Lu, Xiyan,Lei, Aiwen
, p. 9237 - 9246 (2007/10/03)
A highly enantioselective synthesis of optically active N-tosyl-4-alkyl-1,3-oxazolidin-2-ones based on the asymmetric hydrogenation of the trisubstituted exocyclic double bond of N-tosyl-4-alkylidene-1,3-oxazolidin-2-ones under the catalysis of neutral [R
