Cas 26922-45-2,2,5-Methano-5H,9H-pyrimido[2,1-b][1,5,3]dioxazepin-9-one, 2,3-dihydro-8-methyl-3-[[[(4-methylphenyl)sulfonyl]oxy]methyl]-, (2R,3R,5R)-

26922-45-2

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Basic information

Product Name: 2,5-Methano-5H,9H-pyrimido[2,1-b][1,5,3]dioxazepin-9-one, 2,3-dihydro-8-methyl-3-[[[(4-methylphenyl)sulfonyl]oxy]methyl]-, (2R,3R,5R)-
Synonyms:
CAS NO:26922-45-2
Molecular Formula: C17H18N2O6S
Molecular Weight: 378.406
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2,5-Methano-5H,9H-pyrimido[2,1-b][1,5,3]dioxazepin-9-one, 2,3-dihydro-8-methyl-3-[[[(4-methylphenyl)sulfonyl]oxy]methyl]-, (2R,3R,5R)-(CAS DataBase Reference)
NIST Chemistry Reference: 2,5-Methano-5H,9H-pyrimido[2,1-b][1,5,3]dioxazepin-9-one, 2,3-dihydro-8-methyl-3-[[[(4-methylphenyl)sulfonyl]oxy]methyl]-, (2R,3R,5R)-(26922-45-2)
EPA Substance Registry System: 2,5-Methano-5H,9H-pyrimido[2,1-b][1,5,3]dioxazepin-9-one, 2,3-dihydro-8-methyl-3-[[[(4-methylphenyl)sulfonyl]oxy]methyl]-, (2R,3R,5R)-(26922-45-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 26922-45-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 26922-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,9,2 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 26922-45:
(7*2)+(6*6)+(5*9)+(4*2)+(3*2)+(2*4)+(1*5)=122
122 % 10 = 2
So 26922-45-2 is a valid CAS Registry Number.

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26922-45-2Relevant academic research and scientific papers

Study on disulfur-backboned nucleic acid: Part 2. Efficient synthesis of 3′,5′-dithiothymidine

Wang, Hua,Cheng, Changmei,Zheng, Hongchao,Liu, Xiaohong,Fang, Chang,Xu, Shanshan,Zhao, Yufen

, p. 432 - 433 (2007/10/03)

A novel and convenient procedure for synthesizing 3′,5′- dithiothymidine was described. In this procedure, DBU was used to form the intramolecular ring of 2,3′-anhydrothymidine and then the thioacetic acid was used as solvent as well as the nucleophilic r

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