Cas 194412-10-7,Uridine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-5-[[[2-(4-nitrophenyl) ethoxy]carbonyl]amino]-

194412-10-7

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Basic information

Product Name: Uridine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-5-[[[2-(4-nitrophenyl) ethoxy]carbonyl]amino]-
Synonyms:
CAS NO:194412-10-7
Molecular Formula: C39H38N4O11
Molecular Weight: 738.751
EINECS: N/A
Product Categories: N/A
Mol File: 194412-10-7.mol
Article Data: 1

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: Uridine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-5-[[[2-(4-nitrophenyl) ethoxy]carbonyl]amino]-(CAS DataBase Reference)
NIST Chemistry Reference: Uridine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-5-[[[2-(4-nitrophenyl) ethoxy]carbonyl]amino]-(194412-10-7)
EPA Substance Registry System: Uridine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-5-[[[2-(4-nitrophenyl) ethoxy]carbonyl]amino]-(194412-10-7)

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: 194412-10-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 194412-10-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,4,1 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 194412-10:
(8*1)+(7*9)+(6*4)+(5*4)+(4*1)+(3*2)+(2*1)+(1*0)=127
127 % 10 = 7
So 194412-10-7 is a valid CAS Registry Number.

194412-10-7Upstream product

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194412-10-7Relevant articles and documents

Synthesis of oligodeoxynucleotides containing 5-aminouracil and its N-acetyl derivative

Ferrer, Elisenda,Neubauer, Gitte,Mann, Matthias,Eritja, Ramon

, p. 2051 - 2057 (2007/10/03)

The preparation of oligonucleotides containing 5-amino-2′-deoxyuridine is described. Three different protective groups for the amino function of 5-aminouracil including trifluoroacetyl, dimethylformamidine and 2-(4-nitrophenyl)ethoxycarbonyl are analysed

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