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(2R,3R,4R,5R)-3,4-bis(benzoyloxy)-5-((benzoyloxy)methyl)tetrahydrofuran-2-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23316-68-9

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  • (2R,3R,4R,5R)-3,4-bis(benzoyloxy)-5-[(benzoyloxy)methyl]oxolane-2-carboxylic acid

    Cas No: 23316-68-9

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23316-68-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23316-68-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,3,1 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 23316-68:
(7*2)+(6*3)+(5*3)+(4*1)+(3*6)+(2*6)+(1*8)=89
89 % 10 = 9
So 23316-68-9 is a valid CAS Registry Number.

23316-68-9Relevant articles and documents

COMPOUNDS AS CD73 INHIBITORS

-

, (2021/05/15)

Provided herein are the compounds that are inhibitors of CD73 and are useful in treating CD73-associated diseases or conditions. Compositions containing the compounds are also provided.

Highly stereoselective synthesis of aryl/heteroaryl-: C -nucleosides via the merger of photoredox and nickel catalysis

Ma, Yingying,Liu, Shihui,Xi, Yifan,Li, Hongrui,Yang, Kai,Cheng, Zhihao,Wang, Wei,Zhang, Yongqiang

, p. 14657 - 14660 (2019/12/11)

A photoredox/nickel dual-catalyzed decarboxylative cross-coupling reaction of anomeric ribosyl/deoxyribosyl acids with aryl/heteroaryl bromides has been developed. The reaction proceeds smoothly under visible-light irradiation and features the using of cost-effective and easily handled catalysts and starting materials, which allows the highly stereoselective synthesis of diverse aryl/heteroaryl-C-nucleosides in moderate to high yields.

Synthesis of C-ribosyl 1,2,4-triazolo[3,4-f][1,2,4]triazines as inhibitors of adenosine and AMP deaminases

Dudfield, Philip J.,Le, Van-Duc,Lindell, Stephen D.,Rees, Charles W.

, p. 2937 - 2942 (2007/10/03)

Modified C-nucleosides and nucleotides with an enhanced tendency to undergo covalent hydration are of interest as potential inhibitors of adenosine deaminase (ADA) and AMP deaminase, respectively. In a search for such compounds we have synthesized 6-dimet

Synthesis of 1-chloroacetyl-1-dehydroxy-2,3,5-tri-O-benzoyl-β-D-ribofuranose. A potentially versatile intermediate for the synthesis of C-nucleosides

Han,Lee,Kang,Kim,Chi

, p. 2815 - 2822 (2007/10/02)

New key carbohydrate intermediate, 1-chloroacetyl-1-dehydroxy-2,3,5-tri-O-benzoyl-β-D-ribofuranose (1a) has been synthesized. The application of this key intermediate would be very wide. We have very conveniently synthesized several C-nucleosides includin

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