Cas 936739-67-2,3-N-(9-fluorenylmethoxycarbonyl)amino-4-[(5'-O-4,4'-dimethoxytriphenyl)methyl-2'-deoxy-β-D-ribofuranosyl]biphenyl

936739-67-2

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Basic information

Product Name: 3-N-(9-fluorenylmethoxycarbonyl)amino-4-[(5'-O-4,4'-dimethoxytriphenyl)methyl-2'-deoxy-β-D-ribofuranosyl]biphenyl
Synonyms: 3-N-(9-fluorenylmethoxycarbonyl)amino-4-[(5'-O-4,4'-dimethoxytriphenyl)methyl-2'-deoxy-β-D-ribofuranosyl]biphenyl
CAS NO:936739-67-2
Molecular Formula:
Molecular Weight: 809.959
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: 3-N-(9-fluorenylmethoxycarbonyl)amino-4-[(5'-O-4,4'-dimethoxytriphenyl)methyl-2'-deoxy-β-D-ribofuranosyl]biphenyl(CAS DataBase Reference)
NIST Chemistry Reference: 3-N-(9-fluorenylmethoxycarbonyl)amino-4-[(5'-O-4,4'-dimethoxytriphenyl)methyl-2'-deoxy-β-D-ribofuranosyl]biphenyl(936739-67-2)
EPA Substance Registry System: 3-N-(9-fluorenylmethoxycarbonyl)amino-4-[(5'-O-4,4'-dimethoxytriphenyl)methyl-2'-deoxy-β-D-ribofuranosyl]biphenyl(936739-67-2)

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: 936739-67-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 936739-67-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,6,7,3 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 936739-67:
(8*9)+(7*3)+(6*6)+(5*7)+(4*3)+(3*9)+(2*6)+(1*7)=222
222 % 10 = 2
So 936739-67-2 is a valid CAS Registry Number.

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936739-67-2Relevant academic research and scientific papers

A fluorescence-quencher pair for DNA hybridization studies based on hydrophobic base surrogates

Stoop, Matthias,Zahn, Alain,Leumann, Christian J.

, p. 3440 - 3449 (2007/10/03)

The synthesis of the novel, fluorescent 3-aminobiphenyl-C-nucleoside M as well as the corresponding building block for oligodeoxynucleotide synthesis is described. M was incorporated into oligodeoxynucleotides via standard phosphoramidite chemistry and th

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