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Uridine, 2-deoxy-5-fluoro, 3,5-di-9-octadecenoate, (Z,Z)- is a complex organic compound that combines elements of nucleosides and fatty acids. It is a derivative of uridine, a nucleoside that is a component of RNA, with a 2-deoxy-5-fluoro modification, which replaces a hydroxyl group with a fluorine atom at the 5-position and removes an oxygen atom at the 2-position. The compound is further characterized by the presence of two (Z,Z)-9-octadecenoate moieties, which are fatty acid chains with two double bonds in the Z configuration, attached at the 3 and 5 positions. This unique structure may have implications for its biological activity and potential applications in医药领域, such as in the development of antiviral or anticancer drugs, due to its ability to interfere with nucleic acid synthesis or function.

7207-70-7

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7207-70-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7207-70-7 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, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7207-70:
(6*7)+(5*2)+(4*0)+(3*7)+(2*7)+(1*0)=87
87 % 10 = 7
So 7207-70-7 is a valid CAS Registry Number.

7207-70-7SDS

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 3',5'-di-O-oleoyl-FUdR

1.2 Other means of identification

Product number -
Other names -

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:7207-70-7 SDS

7207-70-7Downstream Products

7207-70-7Relevant 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

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