Cas 872428-36-9,Cytidine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-(2-cyanoethyl)-, 3'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite]

872428-36-9

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Basic information

Product Name: Cytidine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-(2-cyanoethyl)-, 3'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite]
Synonyms:
CAS NO:872428-36-9
Molecular Formula: C42H51N6O8P
Molecular Weight: 798.876
EINECS: N/A
Product Categories: N/A
Mol File: 872428-36-9.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: Cytidine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-(2-cyanoethyl)-, 3'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite](CAS DataBase Reference)
NIST Chemistry Reference: Cytidine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-(2-cyanoethyl)-, 3'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite](872428-36-9)
EPA Substance Registry System: Cytidine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-O-(2-cyanoethyl)-, 3'-[2-cyanoethyl bis(1-methylethyl)phosphoramidite](872428-36-9)

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: 872428-36-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 872428-36-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,4,2 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 872428-36:
(8*8)+(7*7)+(6*2)+(5*4)+(4*2)+(3*8)+(2*3)+(1*6)=189
189 % 10 = 9
So 872428-36-9 is a valid CAS Registry Number.

872428-36-9Upstream product

872428-36-9Downstream Products

864837-22-9 4-N-acetyl-2'-O-(2-cyanoethyl)-5'-O-(4,4'-dimethoxytrityl)cytidine 3'-(N,N-diisopropyl)phosphoramidite

872428-36-9Relevant articles and documents

Facile synthesis of 2′-O-cyanoethyluridine by ring-opening reaction of 2,2′-anhydrouridine with cyanoethyl trimethylsilyl ether in the presence of BF3·Et2O

Saneyoshi, Hisao,Okamoto, Itaru,Masaki, Yoshiaki,Ohkubo, Akihiro,Seio, Kohji,Sekine, Mitsuo

, p. 8554 - 8557 (2007)

In this Letter, a facile method for the synthesis of 2′-O-cyanoethyluridine, which is a key intermediate in the synthesis of fully and partially 2′-O-cyanoethylated oligoribonucleotides as well as unmodified oligoribonucleotides, was developed by the ring

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