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Uridine,2'-deoxy-5-(3-phenyl-5-isoxazolyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

133070-83-4

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133070-83-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133070-83-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,0,7 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 133070-83:
(8*1)+(7*3)+(6*3)+(5*0)+(4*7)+(3*0)+(2*8)+(1*3)=94
94 % 10 = 4
So 133070-83-4 is a valid CAS Registry Number.

133070-83-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(3-phenylisoxazol-5-yl)-2'-deoxyuridine

1.2 Other means of identification

Product number -
Other names 1-((2R,4S,5R)-4-Hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-5-(3-phenyl-isoxazol-5-yl)-1H-pyrimidine-2,4-dione

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:133070-83-4 SDS

133070-83-4Downstream Products

133070-83-4Relevant academic research and scientific papers

C5-Modified nucleosides exhibiting anticancer activity

Lee, Yoon-Suk,Park, Sun Min,Kim, Hwan Mook,Park, Song-Kyu,Lee, Kiho,Lee, Chang Woo,Kim, Byeang Hyean

scheme or table, p. 4688 - 4691 (2010/04/28)

We describe (i) a simple method for the synthesis of C5-modified nucleosides from 5-iodo-2′-deoxyuridine and (ii) their activity against six types of human cancer cell lines (HCT15, MM231, NCI-H23, NUGC-3, PC-3, ACHN). We generated nitrile oxides in situ from oximes using a commercial bleaching agent; their cycloadditions with 5-ethynyl-2′-deoxyuridine yielded isoxazole derivatives possessing activity against the cancer cell lines. We synthesized several azides from benzylic bromides and their click reactions with 5-ethynyl-2′-deoxyuridine provided triazole derivatives.

Synthesis and Antiviral Activity of 5-Heteroaryl-Substituted 2'-Deoxyuridines

Wigerinck, P.,Snoeck, R.,Claes, P.,Clercq, E. De,Herdewijn, P.

, p. 1767 - 1772 (2007/10/02)

The synthesis of 5-heteroaryl-substituted 2'-deoxyuridines is described.The heteroaromatics were obtained from three different 5-substituted 2-deoxyuridines.Cycloaddition reaction of nitrile oxides on the 5-ethynyl derivative 1 gave the isoxazoles 4a-e.Th

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