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(S)-2-Benzyloxycarbonylamino-6-hydroxyamino-hexanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

171287-56-2

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171287-56-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 171287-56-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,2,8 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 171287-56:
(8*1)+(7*7)+(6*1)+(5*2)+(4*8)+(3*7)+(2*5)+(1*6)=142
142 % 10 = 2
So 171287-56-2 is a valid CAS Registry Number.

171287-56-2Relevant academic research and scientific papers

Total Synthesis of the Proposed Structure of Mycobactin J

Ghosh, Chiranjit,Pal, Sujit,Patel, Akanksha,Kapur, Manmohan

supporting information, p. 6511 - 6515 (2018/10/20)

The total synthesis of the proposed structure of mycobactin J (MJ), a metabolite of Mycobacterium tuberculosis, is presented. The highlights of the synthesis include a careful control of the Z-stereochemistry of the unsaturated long chain fatty acid, a biomimetic construction of the oxazoline building block and the carriage of an unprotected phenol throughout the synthesis.

Synthesis and studies of catechol-containing mycobactin S and T analogs

Walz, Andrew J.,Moellmann, Ute,Miller, Marvin J.

, p. 1621 - 1628 (2008/02/07)

The syntheses of catechol-containing mycobactin S and T analogs are described. These analogs incorporate a catechol-glycine moiety in place of the phenol-oxazoline of the naturally occurring mycobactins S and T. Studies indicated that the new siderophore

Synthesis and Biological Activity of Hydroxamic Acid-Derived Vasopeptidase Inhibitor Analogues

Walz, Andrew J.,Miller, Marvin J.

, p. 2047 - 2050 (2007/10/03)

(Equation Presented) Syntheses of novel hydroxamic acid-derived azepinones containing pendant mercaptoacyl groups or formyl hydroxamates are described. These new analogues of therapeutically important ACE and NEP inhibitors include unprecedented changes a

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