Cas 112105-22-3,1-<2'-O-Phenoxythiocarbonyl-3',5'-O-(tetraisopropyldisiloxan-1,3-diyl)-β-D-ribofuranosyl>-5-(tert.butylamino)-tetrazol

112105-22-3

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Basic information

Product Name: 1-<2'-O-Phenoxythiocarbonyl-3',5'-O-(tetraisopropyldisiloxan-1,3-diyl)-β-D-ribofuranosyl>-5-(tert.butylamino)-tetrazol
Synonyms:
CAS NO:112105-22-3
Molecular Formula:
Molecular Weight: 651.975
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: 1-<2'-O-Phenoxythiocarbonyl-3',5'-O-(tetraisopropyldisiloxan-1,3-diyl)-β-D-ribofuranosyl>-5-(tert.butylamino)-tetrazol(CAS DataBase Reference)
NIST Chemistry Reference: 1-<2'-O-Phenoxythiocarbonyl-3',5'-O-(tetraisopropyldisiloxan-1,3-diyl)-β-D-ribofuranosyl>-5-(tert.butylamino)-tetrazol(112105-22-3)
EPA Substance Registry System: 1-<2'-O-Phenoxythiocarbonyl-3',5'-O-(tetraisopropyldisiloxan-1,3-diyl)-β-D-ribofuranosyl>-5-(tert.butylamino)-tetrazol(112105-22-3)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 112105-22-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 112105-22-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,1,0 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 112105-22:
(8*1)+(7*1)+(6*2)+(5*1)+(4*0)+(3*5)+(2*2)+(1*2)=53
53 % 10 = 3
So 112105-22-3 is a valid CAS Registry Number.

112105-22-3Upstream product

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112105-22-3Relevant academic research and scientific papers

Glykosylazides as Starting Materials for the Preparation of Nucleoside Analogues, Part III: Syntheses of Alkylaminotetrazole- and Uretidino Nucleosides

Knotz, Herbert,Zbiral, Erich

, p. 1437 - 1460 (1986)

The β-ribofuranosylazide 1 is transformed after usual derivatization by suitable protecting groups into the P-N-ylid 2, which gives the corresponding N-Glykosyl-N-alkylcarbodiimides 4 and a small amount of the glykosylisocyanatderivative 3 by reaction wit

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