Cas 359785-71-0,2-(4-methoxyphenyl)-O<sup>6</sup>-benzyl-3',5'-bis-O-(tert-butyldimethylsilyl)-2'-deoxyinosine

359785-71-0

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Basic information

Product Name: 2-(4-methoxyphenyl)-O⁶-benzyl-3',5'-bis-O-(tert-butyldimethylsilyl)-2'-deoxyinosine
Synonyms: 2-(4-methoxyphenyl)-O⁶-benzyl-3',5'-bis-O-(tert-butyldimethylsilyl)-2'-deoxyinosine
CAS NO:359785-71-0
Molecular Formula:
Molecular Weight: 677.004
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: 2-(4-methoxyphenyl)-O⁶-benzyl-3',5'-bis-O-(tert-butyldimethylsilyl)-2'-deoxyinosine(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4-methoxyphenyl)-O⁶-benzyl-3',5'-bis-O-(tert-butyldimethylsilyl)-2'-deoxyinosine(359785-71-0)
EPA Substance Registry System: 2-(4-methoxyphenyl)-O⁶-benzyl-3',5'-bis-O-(tert-butyldimethylsilyl)-2'-deoxyinosine(359785-71-0)

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: 359785-71-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 359785-71-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,9,7,8 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 359785-71:
(8*3)+(7*5)+(6*9)+(5*7)+(4*8)+(3*5)+(2*7)+(1*1)=210
210 % 10 = 0
So 359785-71-0 is a valid CAS Registry Number.

359785-71-0Upstream product

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359785-71-0Relevant academic research and scientific papers

Palladium catalysis for the synthesis of hydrophobic C-6 and C-2 aryl 2′-deoxynucleosides. Comparison of C-C versus C-N bond formation as well as C-6 versus C-2 reactivity

Lakshman,Hilmer,Martin,Keeler,Dinh,Ngassa,Russon

, p. 7779 - 7787 (2001)

Suzuki-Miyaura cross-coupling of haloaromatic compounds with arylboronic acids provides a simple entry to biaryl systems. Despite its ease, to date, there are no detailed investigations of this procedure for deoxynucleoside modification. As shown in this

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