Cas 1174403-00-9,N-(dimethylacetamidine)-5'-O-(4,4'-dimethoxytriphenylmethyl)-2'-deoxy-2'-triphenylmethylthioadenosine

1174403-00-9

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Basic information

Product Name: N-(dimethylacetamidine)-5'-O-(4,4'-dimethoxytriphenylmethyl)-2'-deoxy-2'-triphenylmethylthioadenosine
Synonyms: N-(dimethylacetamidine)-5'-O-(4,4'-dimethoxytriphenylmethyl)-2'-deoxy-2'-triphenylmethylthioadenosine
CAS NO:1174403-00-9
Molecular Formula:
Molecular Weight: 897.11
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: N-(dimethylacetamidine)-5'-O-(4,4'-dimethoxytriphenylmethyl)-2'-deoxy-2'-triphenylmethylthioadenosine(CAS DataBase Reference)
NIST Chemistry Reference: N-(dimethylacetamidine)-5'-O-(4,4'-dimethoxytriphenylmethyl)-2'-deoxy-2'-triphenylmethylthioadenosine(1174403-00-9)
EPA Substance Registry System: N-(dimethylacetamidine)-5'-O-(4,4'-dimethoxytriphenylmethyl)-2'-deoxy-2'-triphenylmethylthioadenosine(1174403-00-9)

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: 1174403-00-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1174403-00-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,4,4,0 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1174403-00:
(9*1)+(8*1)+(7*7)+(6*4)+(5*4)+(4*0)+(3*3)+(2*0)+(1*0)=119
119 % 10 = 9
So 1174403-00-9 is a valid CAS Registry Number.

1174403-00-9Upstream product

1174403-00-9Downstream Products

1174403-02-1 C₆₃H₆₉N₈O₆PS

1174403-00-9Relevant academic research and scientific papers

Synthesis and evaluation of an RNA editing substrate bearing 2′-deoxy-2′-mercaptoadenosine

Jayalath, Prasanna,Pokharel, Subhash,Veliz, Eduardo,Beal, Peter A.

experimental part, p. 78 - 88 (2009/05/30)

The RNA-editing adenosine deaminases (ADARs) catalyze deamination of adenosine to inosine in double stranded structure found in various RNA substrates, including mRNAs. Here we describe the synthesis of a phosphoramidite of 2′-deoxy-2′-mercaptoadenosine a

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