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59240-49-2

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59240-49-2 Usage

General Description

1-Pentofuranosyl-5-(prop-2-en-1-yl)pyrimidine-2,4(1H,3H)-dione is a chemical compound with a complex and lengthy name. It is a pyrimidine derivative with a sugar moiety attached, and it possesses a dihydropyrimidinone structure. 1-pentofuranosyl-5-(prop-2-en-1-yl)pyrimidine-2,4(1H,3H)-dione is of interest in the field of medicinal chemistry due to its potential biological activities and pharmacological properties. Its structure suggests that it may have antiviral, antifungal, or antibacterial properties, and it could potentially be developed into a therapeutic agent for various diseases. Further research is needed to fully understand the properties and potential applications of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 59240-49-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,2,4 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 59240-49:
(7*5)+(6*9)+(5*2)+(4*4)+(3*0)+(2*4)+(1*9)=132
132 % 10 = 2
So 59240-49-2 is a valid CAS Registry Number.

59240-49-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-prop-2-enylpyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 5-allyl-uridine

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:59240-49-2 SDS

59240-49-2Downstream Products

59240-49-2Relevant articles and documents

Photochemistry of 5- and 6-Iodouracils in the Presence of Allylsilanes and Alkenes. A Convenient Route to C5- and C6-Substituted Uracils

Saito, Isao,Ikehira, Hideyuki,Matsuura, Teruo

, p. 5148 - 5153 (2007/10/02)

The photocoupling reaction of 5- and 6-iodouracil derivatives with allylsilanes and alkenes is presented.Irradiation of 5-iodouridine (5) and 5-iodo-2'-deoxyuridine (6) in the presence of allyltrimethylsilane in aqueous acetonitrile gave 5-allyluridine (7) and 5-allyl-2'-deoxyuridine, respectively.Irradiation of 6-iodo-1,3-dimethyluracil (11) in the presence of allylsilanes and alkyl-substituted olefins produced the corresponding C6-substituted uracil derivatives in good yields. 5-Fluoro-6-iodo-1,3-dimethyluracil (12) underwent a similar photocoupling reaction with allylsilanes and alkenes.The photocoupling reaction provides a convenient method for carbon-carbon bond formation at the C5 or C6 position of uracil derivatives.A radical addition mechanism has been proposed for this novel photocoupling reaction.

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