Cas 1135615-89-2,1-phenylsulfonyl-3-[2'-deoxy-5'-O-(4,4'-dimethoxytrityl)-β-D-ribofuranosyl]indole

1135615-89-2

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Basic information

Product Name: 1-phenylsulfonyl-3-[2'-deoxy-5'-O-(4,4'-dimethoxytrityl)-β-D-ribofuranosyl]indole
Synonyms: 1-phenylsulfonyl-3-[2'-deoxy-5'-O-(4,4'-dimethoxytrityl)-β-D-ribofuranosyl]indole
CAS NO:1135615-89-2
Molecular Formula:
Molecular Weight: 675.802
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-phenylsulfonyl-3-[2'-deoxy-5'-O-(4,4'-dimethoxytrityl)-β-D-ribofuranosyl]indole(CAS DataBase Reference)
NIST Chemistry Reference: 1-phenylsulfonyl-3-[2'-deoxy-5'-O-(4,4'-dimethoxytrityl)-β-D-ribofuranosyl]indole(1135615-89-2)
EPA Substance Registry System: 1-phenylsulfonyl-3-[2'-deoxy-5'-O-(4,4'-dimethoxytrityl)-β-D-ribofuranosyl]indole(1135615-89-2)

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: 1135615-89-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1135615-89-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,5,6,1 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1135615-89:
(9*1)+(8*1)+(7*3)+(6*5)+(5*6)+(4*1)+(3*5)+(2*8)+(1*9)=142
142 % 10 = 2
So 1135615-89-2 is a valid CAS Registry Number.

1135615-89-2Upstream product

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1135615-90-5 3-[2'-deoxy-5'-O-(4,4'-dimethoxytrityl)-β-D-ribofuranosyl]indole

1135615-89-2Relevant academic research and scientific papers

Indole in DNA: Comparison of a nucleosidic with a non-nucleosidic DNA base substitution

Barbaric, Janez,Wanninger-Weiss, Claudia,Wagenknecht, Hans-Achim

, p. 364 - 370 (2009)

The synthetic incorporation of indole as an artificial DNA base into oligonucleotides by two different structural approaches is described. For both types of modification, the indole moiety is attached through the C-3 position to the oligonucleotides. As a

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