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DL-α-Allyl-Phenylglycin-methylester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

120924-52-9

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120924-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120924-52-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,9,2 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 120924-52:
(8*1)+(7*2)+(6*0)+(5*9)+(4*2)+(3*4)+(2*5)+(1*2)=99
99 % 10 = 9
So 120924-52-9 is a valid CAS Registry Number.

120924-52-9Relevant academic research and scientific papers

Catalytic α-allylation of unprotected amino acid esters

Fang, Ping,Raj Chaulagain, Mani,Aron, Zachary D.

supporting information; experimental part, p. 2130 - 2133 (2012/07/03)

Catalytic α-allylation of unprotected amino acid esters to produce α-quaternary α-allyl amino acid esters is reported. Catalytic loadings of picolinaldehyde and Ni(II) salts induce preferential reactivity at the enolizable α-carbon of amino acid esters ov

The 'unexpected' epimerization on bicyclic thiazolidine γ-lactam scaffolds

Liu, Ruzhang,Wu, Yang,Li, Qiang,Liao, Wensheng,Chen, Shu-Hui,Li, Ge,Betancort, Juan M.,Winn, David T.,Campbell, David A.

, p. 4363 - 4369 (2008/09/21)

Preliminary findings related to the base induced cyclization and spontaneous epimerization leading to stereochemically defined bicyclic thiazolidine γ-lactam systems are reported.

The synthesis of β-strand mimetic templates via regioselective 1,3-dipolar cycloaddition with vinylsulfone

Fuchi, Nobuhiro,Doi, Takayuki,Harada, Takeo,Urban, Jan,Cao, Bolong,Kahn, Michael,Takahashi, Takashi

, p. 1305 - 1308 (2007/10/03)

We have developed a practical synthetic route to constrained β-strand mimetic templates by regioselective 1,3-dipolar cycloaddition of azomethine imines with vinyl sulfone. A small library of β-strand mimetic templates was generated which include potent and selective inhibitors of serine proteases.

Secondary structure peptide mimetics: Design, synthesis, and evaluation of β-strand mimetic thrombin inhibitors

Boatman, P. Douglas,Ogbu, Cyprian O.,Eguchi, Masakatsu,Kim, Hwa-Ok,Nakanishi, Hiroshi,Cao, Bolong,Shea, J. Paul,Kahn, Michael

, p. 1367 - 1375 (2007/10/03)

Constrained dipeptide mimetic templates were designed to mimic the secondary structure of peptides in a β-strand conformation. Two templates corresponding to the D-Phe-Pro portion of the thrombin inhibitor D-Phe-Pro- ArgCH2Cl were synthesized a

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