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threo-methyl 2-((tert-butoxycarbonyl)amino)-3-hydroxy-3-phenylpropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

439612-08-5

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439612-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 439612-08-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,9,6,1 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 439612-08:
(8*4)+(7*3)+(6*9)+(5*6)+(4*1)+(3*2)+(2*0)+(1*8)=155
155 % 10 = 5
So 439612-08-5 is a valid CAS Registry Number.

439612-08-5Relevant academic research and scientific papers

GLP-1 RECEPTOR MODULATORS

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Paragraph 00791, (2016/06/28)

Compounds are provided that modulate the glucagon-like peptide 1 (GLP-1) receptor, as well as methods of their synthesis, and methods of their therapeutic and/or prophylactic use. Such compounds can act as modulators or potentiators of GLP-1 receptor on their own, or with incretin peptides such as GLP-1(7-36) and GLP-1(9-36), or with peptide-based therapies, such as exenatide and liraglutide, and have the following general structure (where "^^^^" represents either or both the R and S form of the compound) (I) where A, B, C, Y1, Y2, Z, R1, R2, R3, R4, R5, W1, n, p and q are as defined herein.

IMPROVED AMINOHYDROXYLATION OF ALKENES

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Page/Page column 59, (2012/01/06)

The invention relates to a process for the aminohydroxylation of alkenes using N-oxycarbamate reagents, e.g. N-acyloxycarbamate, N-alkyloxycarbonyloxycarbamate and N-aralkoxycarbonyloxycarbamate reagents. The invention particularly relates to an intermolecular aminohydroxylation reaction that can be carried out in the absence of added base. The invention also relates to novel N-oxycarbamate reagents that are stable crystalline materials. The process of the invention is useful in the synthesis of compounds having a vicinal amino alcohol moiety, such as biologically active compounds.

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