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(S)-tert-butyl (1-oxo-3-phenyl-1-(prop-2-yn-1-ylamino)propan-2-yl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

461638-99-3

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461638-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 461638-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,1,6,3 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 461638-99:
(8*4)+(7*6)+(6*1)+(5*6)+(4*3)+(3*8)+(2*9)+(1*9)=173
173 % 10 = 3
So 461638-99-3 is a valid CAS Registry Number.

461638-99-3Relevant academic research and scientific papers

Transformation of helical sense of poly(N-propargylamides) controlled by competition between structurally different enantiomeric amino acids

Zhao, Haichao,Sanda, Fumio,Masuda, Toshio

, p. 8888 - 8892 (2004)

Copolymerizations of structurally different chiral amino acid-based N-propargylamides, N-(tert-butoxycarbonyl)-D-alanine-N-propargylamide (DA) with either N-(tert-butoxycarbonyl)-L-valine-N-propargylamide (LV) or N-(tert-butoxycarbonyl)-L-phenylalanine-N-

Optically active amino acid-based polyacetylenes: Effect of tunable helical conformation on infrared emissivity property

Bu, Xiaohai,Zhou, Yuming,Chen, Zhenjie,He, Man,Zhang, Tao

, p. 17 - 24 (2014)

Chiral amino acid-based monosubstituted acetylene monomers [N-tert-butoxy-carbonyl-l-phenylalanine-N′-propargylamide (LP), and N-tert-butoxycarbonyl-l-serine-N′-propargylamide (LS)] were (co)polymerized with rhodium zwitterion catalyst in THF to afford he

Expressed Protein Ligation without Intein

Kratch, Kaci C.,Leeuwon, Sunshine Z.,Liu, Wenshe Ray,Morse, Jared S.,Qiao, Yuchen,Wang, Wesley Wei,Wang, Xiaoyan Aria,Xu, Shiqing,Yu, Ge

supporting information, p. 7047 - 7054 (2020/05/14)

Proteins with a functionalized C-terminus such as a C-terminal thioester are key to the synthesis of larger proteins via expressed protein ligation. They are usually made by recombinant fusion to intein. Although powerful, the intein fusion approach suffe

Synthesis and Reversible Hydration of a Pseudoprotein, a Fully Organic Polymeric Desiccant by Multiple Single-Crystal-to-Single-Crystal Transformations

Mohanrao, Raja,Sureshan, Kana M.

supporting information, p. 12435 - 12439 (2018/09/10)

A diphenylalanine derivative, N3-Phe-Phe-NHCH2CCH, was designed for topochemical azide–alkyne cycloaddition (TAAC) polymerization. This dipeptide adopted β-sheet arrangement as designed, in its crystals, but the azide and alkyne were not fitly aligned for

Chemical probes for competitive profiling of the quorum sensing signal synthase PqsD of Pseudomonas aeruginosa

Prothiwa, Michaela,Szamosvári, Dávid,Glasmacher, Sandra,B?ttcher, Thomas

supporting information, p. 2784 - 2792 (2017/01/09)

The human pathogen Pseudomonas aeruginosa uses the pqs quorum sensing system to coordinate the production of its broad spectrum of virulence factors to facilitate colonization and infection of its host. Hereby, the enzyme PqsD is a virulence related quoru

A magnetoclick imidazolidinone nanocatalyst for asymmetric 1,3-dipolar cycloadditions

Pagoti, Sreenivasarao,Dutta, Debasish,Dash, Jyotirmayee

supporting information, p. 3532 - 3538 (2014/01/06)

A 1,3-dipolar azide-alkyne cycloaddition has been used to prepare a magnetic nanoparticle immobilized MacMillan catalyst that catalyzes the enantioselective 1,3-dipolar cycloaddition between nitrones and α,β-unsaturated aldehydes. The catalyst can be recovered and recycled for five consecutive runs without any significant loss in yields and diastereo- and enantioselectivities of the isoxazolidines. Copyright

IAP ANTAGONISTS

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Paragraph 00286, (2014/01/09)

There are disclosed compounds that modulate the activity of inhibitors of apoptosis (IAPs), pharmaceutical compositions containing said compounds and methods of treating proliferative disorders and disorders of dysregulated apoptosis, such as cancer, utilizing the compounds of the invention.

Using click chemistry to access mono- and ditopic β-cyclodextrin hosts substituted by chiral amino acids

Tran, Diem Ngan,Blaszkiewicz, Claire,Menuel, Stéphane,Roucoux, Alain,Philippot, Karine,Hapiot, Frédéric,Monflier, Eric

experimental part, p. 210 - 218 (2011/03/18)

A wide range of chiral mono- and ditopic cyclodextrin-based receptors have been synthesized by CuI-catalyzed azide-alkyne cycloaddition starting from mono-6-azido-β-cyclodextrin and chiral amino acids. Of interest, microwaves proved very efficient to acce

Gold-catalysed synthesis of amino acid-derived 2,5-disubstituted oxazoles

Paradise, Christopher L.,Sarkar, Pooja R.,Razzak, Mina,De Brabander, Jef K.

supporting information; experimental part, p. 4017 - 4020 (2011/07/29)

Amino acid-derived propargylic amides are cyclised in a one-pot, Au(iii)-catalysed operation to yield 5-bromomethyl oxazoles. These compounds are further elaborated to bis-heterocycles, dipeptide mimics and more.

CuAAC macrocyclization: High intramolecular selectivity through the use of copper-tris(triazole) ligand complexes

Chouhan, Gagan,James, Keith

supporting information; experimental part, p. 2754 - 2757 (2011/06/26)

A range of multivalent heteroaryl ligands, copper sources, and solvent systems have been investigated for use in CuAAC-mediated macrocyclization reactions. These studies have revealed the key factors governing selectivity for macrocyclization versus dimerization and identified a simple but specific set of reaction conditions capable of efficiently generating a diverse series of drug-like macrocycles at modest dilution in up to 95% yield.

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