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Uridine, 5-(phenylethynyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

649558-84-9

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649558-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 649558-84-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,9,5,5 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 649558-84:
(8*6)+(7*4)+(6*9)+(5*5)+(4*5)+(3*8)+(2*8)+(1*4)=219
219 % 10 = 9
So 649558-84-9 is a valid CAS Registry Number.

649558-84-9SDS

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 1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-(2-phenylethynyl)pyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 5-phenylethynyluridine

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:649558-84-9 SDS

649558-84-9Downstream Products

649558-84-9Relevant academic research and scientific papers

The synthesis and antituberculosis activity of 5-alkynyl uracil derivatives

Platonova, Yana B.,Tomilova, Larisa G.,Volov, Alexander N.

supporting information, (2020/06/26)

A series of new 5-alkynyl-substituted uracil and uridine derivatives were synthesised via palladium-catalysed Sonogashira cross-coupling reaction of 5-bromo-pyrimidine base with terminal acetylenes with good yields in DMF at room temperature. All obtained compounds were tested for antimycobacterial activity against Mycobacetrium bovis and Mycobacterium tuberculosis (H37Ra) at concentrations of 1–100 μg/ml using MABA test. Obtained results revealed that most of tested uracil derivatives exhibited high antimycobacterial activity (MIC50 = 1.1–19.2 μg/ml) in comparison with therapeutic agents such as rifampicin, isoniazid and D-cycloserine, excluding compounds having alkyl substituent at triple alkyne bond.

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