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4-amino-1-[4-hydroxy-5-(hydroxymethyl)-3-[(4-methoxyphenyl)methoxy]oxolan-2-yl]pyrimidin-2-one
Cas No: 80015-55-0
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Dayang Chem (Hangzhou) Co.,Ltd.
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4-amino-1-[4-hydroxy-5-(hydroxymethyl)-3-[(4-methoxyphenyl)methoxy]oxolan-2-yl]pyrimidin-2-one cas 80015-55-0
Cas No: 80015-55-0
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Hangzhou Fandachem Co.,Ltd
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80015-55-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80015-55-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,0,1 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 80015-55:
(7*8)+(6*0)+(5*0)+(4*1)+(3*5)+(2*5)+(1*5)=90
90 % 10 = 0
So 80015-55-0 is a valid CAS Registry Number.

80015-55-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name	4-amino-1-[4-hydroxy-5-(hydroxymethyl)-3-[(4-methoxyphenyl)methoxy]tetrahydrofuran-2-yl]pyrimidin-2-one

1.2 Other means of identification

Product number	-
Other names	2'-O-p-Methoxybenzyladenosine

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:80015-55-0 SDS

80015-55-0Upstream product

80015-55-0Downstream Products

80015-55-0Relevant articles and documents

An Improved Method for the Application of the 4-Methoxybenzyl Group to Protect the 2'-Hydroxyl Group in the Ribonucleotide Synthesis by TFA-acidolysis

Losse, G.,Pechstein, Birgit

, p. 46 - 54 (2007/10/02)

The cleavage of the 4-methoxybenzyl group from the 2'-OH-position of ribonucleosides by the hydrogenation with different Pd-catalysts as well as trifluoroacetic acid has been studied in detail.During hydrogenation, side reactions at the base residue of cytidine occurred which, however, could be extensively suppressed by PdCl2 catalysis.More practicable results were obtained with trifluoroacetic acid in the presence of cation scavengers, allowing smoothly to convert a series of 2'-methoxybenzyl ribonucleotides to the homogeneous deprotection products.

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CAS

80015-55-0