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Phosphoric acid mono-[(2R,3S,4R,5S)-5-(3-carbamoyl-phenyl)-3,4-dihydroxy-tetrahydro-furan-2-ylmethyl] ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138385-30-5

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138385-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138385-30-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,3,8 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 138385-30:
(8*1)+(7*3)+(6*8)+(5*3)+(4*8)+(3*5)+(2*3)+(1*0)=145
145 % 10 = 5
So 138385-30-5 is a valid CAS Registry Number.

138385-30-5Downstream Products

138385-30-5Relevant academic research and scientific papers

Chemoselective and Diastereoselective Synthesis of C-Aryl Nucleoside Analogues by Nickel-Catalyzed Cross-Coupling of Furanosyl Acetates with Aryl Iodides

Li, Chao,Li, Luyang,Li, Yuxi,Shao, Feng,Tian, Xiaoying,Wang, Zheng

supporting information, (2021/11/30)

Canonical nucleosides are vulnerable to enzymatic and chemical degradation, yet their stable mimics—C-aryl nucleosides—have demonstrated potential utility in medicinal chemistry, chemical biology, and synthetic biology, although current synthetic methods remain limited in terms of scope and selectivity. Herein, we report a cross-electrophile coupling to prepare C-aryl nucleoside analogues from readily available furanosyl acetates and aryl iodides. This nickel-catalyzed modular approach is characterized by mild reaction conditions, broad substrate scope, excellent β-selectivity, and high functional-group compatibility. The exclusive chemoselectivity with respect to the aryl iodide enables efficient preparation of a variety of C-aryl halide furanosides suitable for various downstream transformations. The practicality of this transformation is demonstrated through the synthesis of a potent analogue of a naturally occurring NF-κB activator.

Synthesis and cytotoxic activity of C-glycosidic nicotinamide riboside analogues

Krohn,Heins,Wielckens

, p. 511 - 517 (2007/10/02)

The C-glycosidic nicotinamide riboside analogue (2) was prepared by reaction of ribonolactone 24 with the lithiated oxazoline 19 followed by triethylsilane reduction to 26 and deprotection. Selective phosphorylation to the pseudonucleotide 34 was effected

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