Cas 1093660-16-2,N<sub>6</sub>-benzoyl-5'-O-(4,4'-dimethoxytrityl)-8-[3-(4-imidazolyl)propylamino]-2'-deoxyadenosine

1093660-16-2

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Basic information

Product Name: N₆-benzoyl-5'-O-(4,4'-dimethoxytrityl)-8-[3-(4-imidazolyl)propylamino]-2'-deoxyadenosine
Synonyms: N₆-benzoyl-5'-O-(4,4'-dimethoxytrityl)-8-[3-(4-imidazolyl)propylamino]-2'-deoxyadenosine
CAS NO:1093660-16-2
Molecular Formula:
Molecular Weight: 780.883
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: N₆-benzoyl-5'-O-(4,4'-dimethoxytrityl)-8-[3-(4-imidazolyl)propylamino]-2'-deoxyadenosine(CAS DataBase Reference)
NIST Chemistry Reference: N₆-benzoyl-5'-O-(4,4'-dimethoxytrityl)-8-[3-(4-imidazolyl)propylamino]-2'-deoxyadenosine(1093660-16-2)
EPA Substance Registry System: N₆-benzoyl-5'-O-(4,4'-dimethoxytrityl)-8-[3-(4-imidazolyl)propylamino]-2'-deoxyadenosine(1093660-16-2)

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: 1093660-16-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1093660-16-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,3,6,6 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1093660-16:
(9*1)+(8*0)+(7*9)+(6*3)+(5*6)+(4*6)+(3*0)+(2*1)+(1*6)=152
152 % 10 = 2
So 1093660-16-2 is a valid CAS Registry Number.

1093660-16-2Upstream product

129451-79-2 N-(9-{5-[bis(4-methoxyphenyl)phenylmethoxyphenyl]-4-hydroxytetrahydrofuran-2-yl}-8-bromo-9H-purin-6-yl)benzamide

1093660-16-2Downstream Products

1093660-16-2Relevant academic research and scientific papers

Synthesis and enzymatic incorporation of modified deoxyadenosine triphosphates

Lam, Curtis,Hipolito, Christopher,Perrin, David M.

experimental part, p. 4915 - 4923 (2009/05/27)

Several deoxyadenosine triphosphates containing modifications at the 8-position have been synthesized. Suitably protected 8-bromodeoxyadenosines were coupled with five imidazole-containing moieties by nucleophilic aromatic substitution or Sonagashira coup

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