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Uridine 2'-deoxy-5-fluoro-3'-hexadecanoate is a complex chemical compound that combines elements of nucleosides and fatty acids. It is derived from uridine, a nucleoside consisting of a ribose sugar and the base uracil, which plays a crucial role in RNA synthesis. The compound features a 2'-deoxy modification, which means the hydroxyl group at the 2' position of the ribose sugar is replaced by a hydrogen atom, and a 5-fluoro substitution, where a fluorine atom replaces a hydrogen atom at the 5-position of the uracil base. Additionally, it has a 3'-hexadecanoate group attached, which is a long-chain fatty acid with 16 carbon atoms. This unique structure may have potential applications in medicinal chemistry, particularly in the development of antiviral agents, due to its ability to mimic natural nucleosides and interfere with viral replication processes.

96733-84-5

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96733-84-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96733-84-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,7,3 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 96733-84:
(7*9)+(6*6)+(5*7)+(4*3)+(3*3)+(2*8)+(1*4)=175
175 % 10 = 5
So 96733-84-5 is a valid CAS Registry Number.

96733-84-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3'-O-palmitoyl-floxuridine

1.2 Other means of identification

Product number -
Other names 3'-O-palmitoyl-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:96733-84-5 SDS

96733-84-5Downstream Products

96733-84-5Relevant 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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