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5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolane-2-carboxylic acid is a complex organic compound with the molecular formula C8H7N2O7. It is characterized by a pyrimidine ring (2,4-dioxopyrimidin-1-yl) attached to a 3,4-dihydroxy-oxolane-2-carboxylic acid moiety. 5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxy-oxolane-2-carboxylic acid is known for its potential applications in pharmaceutical research, particularly in the development of antiviral and anticancer drugs, due to its ability to interact with nucleic acids. Its structure allows it to form hydrogen bonds and potentially disrupt the replication processes of viruses and癌细胞. The compound's specific activity and mechanism of action would be subject to further investigation in laboratory settings.

3415-07-4

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3415-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3415-07-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,1 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3415-07:
(6*3)+(5*4)+(4*1)+(3*5)+(2*0)+(1*7)=64
64 % 10 = 4
So 3415-07-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H10N2O7/c12-3-1-2-11(9(17)10-3)7-5(14)4(13)6(18-7)8(15)16/h1-2,4-7,13-14H,(H,15,16)(H,10,12,17)

3415-07-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolane-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names uridine-5'-carboxylic acid

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

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More Details:3415-07-4 SDS

3415-07-4Relevant academic research and scientific papers

SYNTHESIS AND TRANSFORMATION OF DERIVATIVES OF THE N- AND O-GLYCOSIDES OF D-RIBOFURANOIC ACID

Timoshchuk, V. A.

, p. 1198 - 1204 (2007/10/02)

A method was developed for the nonselective oxidation of pyrimidine nucleosides and methyl β-D-ribofuranoside to the uronic acids by successive treatment first with triphenylchloromethane and then with acetic anydride in pyridine, followed by oxidation with chromic anhydride in acetone in the presence of sulfuric acid.The transformations of the obtained uronic acids into anhydronucleosides by the action of phthalimide and into 3',4'-unsaturated nucleosides by the action of 1,5-diazabicycloundec-5-ene are described.

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