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(2R,3S)-methyl 2-acetoxy-3-bromo-3-phenylpropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

167357-61-1

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167357-61-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 167357-61-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,3,5 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 167357-61:
(8*1)+(7*6)+(6*7)+(5*3)+(4*5)+(3*7)+(2*6)+(1*1)=161
161 % 10 = 1
So 167357-61-1 is a valid CAS Registry Number.

167357-61-1Relevant academic research and scientific papers

Cystobactamids 920-1 and 920-2: Assignment of the Constitution and Relative Configuration by Total Synthesis

Planke, Therese,Moreno, María,Hüttel, Stephan,Fohrer, J?rg,Gille, Franziska,Norris, Matthew D.,Siebke, Maik,Wang, Liangliang,Müller, Rolf,Kirschning, Andreas

, p. 1359 - 1363 (2019)

Total synthesis of cystobactamid 920-1 and its epimer has allowed an unambiguous assignment of the relative and absolute configuration of the natural product. A careful structural analysis of each isomer using both NMR and computational techniques also pr

CYSTOBACTAMIDES

-

, (2016/06/13)

The present invention provides cystobactamides of formula (I) and the use thereof for the treatment or prophylaxis of bacterial infections:

PROCESS FOR PREPARING TAXOL SIDE CHAIN USING HETEROGENEOUS TRIFUNCTIONAL CATALYST

-

Page 6, (2008/06/13)

The present invention relates to an improved process for the preparation of taxol side chain by synthesizing (2R,3S)-2,3-dihydroxy-3-phenylpropionate with greater than 99% enantioselectivity and devoid of osmium even in crude form in a single pot using a recyclable multifunctional catalysts, conversion of diol obtained without further crystallization into bromoacetate, reaction of bromoacetate with NaN3 in organic solvent followed by deacetylation with to obtain azido alcohol, benzoylation followed by hydrogenation of azido alcohol to obtain the (2R,3S)-(N-)-benzoyl-3-phenylisoserine methyl ester in 67% yield.

An efficient synthesis of alterobactin A; a super siderophore of marine origin

Deng,Hamada,Shioiri

, p. 627 - 638 (2007/10/03)

Alterobactin A (1), a cyclic depsipeptide and a super siderophore isolated from an open-ocean bacterium, was efficiently synthesized for the first time by a convergent manner with the maximum protection of various functional groups.

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