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3',5'-O-dipalmitoyl-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 uridine, with modifications that include the addition of a fluorine atom at the 5-position, the removal of the 2'-hydroxyl group, and the attachment of two palmitoyl groups at the 3' and 5' positions of the sugar moiety. These modifications are designed to enhance the compound's stability, cellular uptake, and potential therapeutic effects. The compound is of interest in medicinal chemistry and drug development, particularly for its potential applications in antiviral and anticancer therapies, due to its ability to interfere with nucleic acid synthesis and function.

7207-68-3

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7207-68-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7207-68-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,0 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7207-68:
(6*7)+(5*2)+(4*0)+(3*7)+(2*6)+(1*8)=93
93 % 10 = 3
So 7207-68-3 is a valid CAS Registry Number.

7207-68-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2R,3S,5R)-5-(5-fluoro-2,4-dioxopyrimidin-1-yl)-3-hexadecanoyl-3-hydroxyoxolan-2-yl]methyl hexadecanoate

1.2 Other means of identification

Product number -
Other names Palmitic acid,diester with2'-deoxy-5-fluorouridine (8CI)

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:7207-68-3 SDS

7207-68-3Downstream Products

7207-68-3Relevant academic research and scientific papers

Regioselective acylation of nucleosides and their analogs catalyzed by Pseudomonas cepacia lipase: enzyme substrate recognition

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

supporting information; experimental part, p. 1063 - 1068 (2009/04/11)

The substrate recognition of Pseudomonas cepacia lipase in the acylation of nucleosides was investigated by means of rational substrate engineering for the first time. P. cepacia lipase displayed excellent 3′-regioselectivities (96 to >99%) in the lauroyl

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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