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Adenosine, 2-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

266360-65-0

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266360-65-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 266360-65-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,6,3,6 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 266360-65:
(8*2)+(7*6)+(6*6)+(5*3)+(4*6)+(3*0)+(2*6)+(1*5)=150
150 % 10 = 0
So 266360-65-0 is a valid CAS Registry Number.

266360-65-0SDS

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 (2R,3R,4S,5R)-2-(6-amino-2-nitropurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol

1.2 Other means of identification

Product number -
Other names Adenosine,2-nitro

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:266360-65-0 SDS

266360-65-0Downstream Products

266360-65-0Relevant academic research and scientific papers

Formation of 2'-deoxy-2-nitroadenosines by reaction of 2'-deoxyadenosines with copper(II) nitrate/acetic anhydride.

Kaiya, Toyo,Tanaka, Haruko,Kohda, Kohfuku

, p. 427 - 433 (2002)

Nitration of 9-substituted [ethyl, (Ac)2-2'-deoxyribosyl, (Ac)3-ribosyl] N6-acetyladenine derivatives with Cu(NO3)2.3H2O/Ac2O was examined. Nitration proceeded at the 2-position, although the yield was low. Removal of the acetyl groups gave 2'-deoxy-2-nitroadenosine derivatives.

Regioselective nitration of purine nucleosides: Synthesis of 2- nitroadenosine and 2-nitroinosine

Deghati, Paymaneh Y. F.,Wanner, Martin J.,Koomen, Gerrit-Jan

, p. 1291 - 1295 (2007/10/03)

Nitration reactions of 6-substituted purine nucleosides with tetrabutylammonium nitrate/trifluoroacetic anhydride (TBAN/TFAA) have been studied. This nitrating mixture selectively nitrates C-6 substituted purines at the 2-position, but the method is limited to substrates without NH or OH substituents. Acetylated 6-chloropurine riboside was cleanly nitrated (DCM, 0°C, 71%) and converted to nitro substituted adenosine and inosine in a few simple steps. (C) 2000 Elsevier Science Ltd.

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