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3',5'-Dioctanoyl-5-fluoro-2'-deoxyuridine is a chemical compound that belongs to the class of nucleoside analogs. It is a derivative of the naturally occurring nucleoside, 2'-deoxyuridine, with modifications that include the addition of two octanoyl groups at the 3' and 5' positions and the presence of a fluorine atom at the 5-position. 3',5'-dioctanoyl-5-fluoro-2'-deoxyuridine is of interest in medicinal chemistry due to its potential antiviral properties, as it can interfere with viral replication by incorporating into viral DNA, leading to chain termination. The octanoyl groups enhance the lipophilicity of the molecule, which may improve its cellular uptake and bioavailability. Research on such compounds is crucial for the development of new antiviral drugs, particularly in the context of emerging viral diseases and drug resistance.

3415-70-1

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3415-70-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3415-70-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,1 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3415-70:
(6*3)+(5*4)+(4*1)+(3*5)+(2*7)+(1*0)=71
71 % 10 = 1
So 3415-70-1 is a valid CAS Registry Number.

3415-70-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3',5'-dioctanoyl-5-fluoro-2'-deoxyuridine

1.2 Other means of identification

Product number -
Other names 3',5'-di-O-octanoyl-FUdR

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:3415-70-1 SDS

3415-70-1Relevant academic research and scientific papers

Regioselective acylation of nucleosides catalyzed by candida antarctica lipase B: Enzyme substrate recognition

Li, Ning,Zong, Min-Hua,Ma, Ding

supporting information; scheme or table, p. 5375 - 5378 (2009/05/07)

The substrate recognition of Candida antarctica lipase B (CAL-B) in the acylation of nucleosides was revealed through rational substrate engineering for the first time. CAL-B displayed lower activities and excellent 5′-regioselectivities (94 to >99%) in t

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