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D-Alanine, trimethylsilyl ester (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79338-42-4

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79338-42-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79338-42-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,3 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79338-42:
(7*7)+(6*9)+(5*3)+(4*3)+(3*8)+(2*4)+(1*2)=164
164 % 10 = 4
So 79338-42-4 is a valid CAS Registry Number.

79338-42-4Relevant academic research and scientific papers

Isostearyl Mixed Anhydrides for the Preparation of N-Methylated Peptides Using C-Terminally Unprotected N-Methylamino Acids

Cary, Douglas R.,Handa, Michiharu,Kobayashi, Yutaka,Kurasaki, Haruaki,Masuya, Keiichi,Matsuda, Ayumu,Matsumoto, Masatoshi,Morimoto, Koki,Nagaya, Akihiro,Nishizawa, Naoki,Taguri, Tomonori,Takeuchi, Hisayuki

supporting information, p. 8039 - 8043 (2020/11/02)

Sustainable and efficient manufacturing methods for N-methylated peptides remain underexplored despite growing interest in therapeutic N-methylated peptides within the pharmaceutical industry. A methodology for the coupling of C-terminally unprotected N-methylamino acids mediated by an isostearic acid halide (ISTAX) and silylating reagent has been developed. This approach allows for the coupling of a wide variety of amino acids and peptides in high yields under mild conditions without the need for a C-terminal deprotection step in the process of C-terminal elongation. These advantages make this a useful synthetic method for the production of peptide therapeutics and diagnostics containing N-methylamino acids.

PROCESSES FOR PREPARING FUNCTIONALIZED CYCLOOCTENES

-

Page/Page column 52-53, (2020/05/19)

The present disclosure relates to processes for preparing functionalized cyclooctenes and the synthetic intermediates prepared thereby.

Synthesis and biological activity of a series of tetrasubstituted- imidazoles as P2X7 antagonists

Gleave, Robert J.,Walter, Daryl S.,Beswick, Paul J.,Fonfria, Elena,Michel, Anton D.,Roman, Shilina A.,Tang, Sac-Pham

scheme or table, p. 4951 - 4954 (2010/10/04)

A series of analogues of the pyrazole lead 1 were synthesized in which the heterocyclic core was replaced with an imidazole. A number of potent antagonists were identified and structure-activity relationships (SAR) were investigated both with respect to activity at the P2X7 receptor and in vitro metabolic stability. Compound 10 was identified as a potent P2X7 antagonist with reduced in vitro metabolism and high solubility.

Dipeptidamides as sweeteners

Unterhalt,Kerckhoff

, p. 165 - 172 (2007/10/03)

Several L-Aspartyl-D-alanin-2-methylcycloalkylamides (9a-h) were synthesized and tested for their sweet quality.

Efficient "One-Pot" Synthesis of N-Trityl Amino Acids

Barlos, Kleomenis,Papaioannou, Dionysios,Theodoropoulos, Dimitrios

, p. 1324 - 1326 (2007/10/02)

A sequential procedure has been developed whereby neutral amino acids 1 were tritylated via their corresponding trimethylsilyl esters 2 to afford, after mild hydrolysis, N-trityl amino acids 3 in high yields and purity.Hydroxy amino acids 4 were preferent

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