Cas 109923-84-4,Hexadecanoic acid {9-((2S,3S,3aR,9aS)-3-hydroxy-5,5,7,7-tetraisopropyl-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-2-yl)-6-[2-(4-nitro-phenyl)-ethoxy]-9H-purin-2-yl}-amide

109923-84-4

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Basic information

Product Name: Hexadecanoic acid {9-((2S,3S,3aR,9aS)-3-hydroxy-5,5,7,7-tetraisopropyl-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-2-yl)-6-[2-(4-nitro-phenyl)-ethoxy]-9H-purin-2-yl}-amide
Synonyms:
CAS NO:109923-84-4
Molecular Formula:
Molecular Weight: 913.315
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: Hexadecanoic acid {9-((2S,3S,3aR,9aS)-3-hydroxy-5,5,7,7-tetraisopropyl-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-2-yl)-6-[2-(4-nitro-phenyl)-ethoxy]-9H-purin-2-yl}-amide(CAS DataBase Reference)
NIST Chemistry Reference: Hexadecanoic acid {9-((2S,3S,3aR,9aS)-3-hydroxy-5,5,7,7-tetraisopropyl-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-2-yl)-6-[2-(4-nitro-phenyl)-ethoxy]-9H-purin-2-yl}-amide(109923-84-4)
EPA Substance Registry System: Hexadecanoic acid {9-((2S,3S,3aR,9aS)-3-hydroxy-5,5,7,7-tetraisopropyl-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-2-yl)-6-[2-(4-nitro-phenyl)-ethoxy]-9H-purin-2-yl}-amide(109923-84-4)

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: 109923-84-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 109923-84-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,9,2 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 109923-84:
(8*1)+(7*0)+(6*9)+(5*9)+(4*2)+(3*3)+(2*8)+(1*4)=144
144 % 10 = 4
So 109923-84-4 is a valid CAS Registry Number.

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109923-84-4Relevant academic research and scientific papers

Synthesis of the mirror image of the RNA fragment D-CAAGG: A model compound to study interactions between oligonucleotides of opposite handedness

Visser, G. M.,van Westrenen, J.,van Boeckel, C. A. A.,van Boom, J. H.

, p. 528 - 537 (2007/10/02)

The pentamer L-CAAGG was prepared starting from properly protected β-L-ribonucleosides via a phosphotriester approach.The identity and chiral purity of the pentamer were established by 1H NMR and CD spectroscopy, respectively.

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