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5,6-dihydro-6-hydroxyuracil is a chemical compound with the molecular formula C4H6N2O3. It is a derivative of uracil, an important pyrimidine base found in RNA. 5,6-dihydro-6-hydroxyuracil is characterized by a dihydro (reduced) and hydroxy (hydroxyl group) modification at the 5,6 positions of the uracil structure. It plays a role in various chemical and biological processes, such as DNA repair and replication, and can be found in certain modified nucleosides and nucleotides. Due to its unique structure, 5,6-dihydro-6-hydroxyuracil has potential applications in the development of new drugs and therapeutics targeting DNA-related diseases.

1194-23-6

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1194-23-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1194-23-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1194-23:
(6*1)+(5*1)+(4*9)+(3*4)+(2*2)+(1*3)=66
66 % 10 = 6
So 1194-23-6 is a valid CAS Registry Number.

1194-23-6SDS

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 5,6-dihydro-6-hydroxyuracil

1.2 Other means of identification

Product number -
Other names 5-hydro-6-hydroxy uracil

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:1194-23-6 SDS

1194-23-6Downstream Products

1194-23-6Relevant academic research and scientific papers

RADIOLYSIS OF DIHYDROURACIL AND DIHYDROTHYMINE IN AQUEOUS SOLUTIONS CONTAINING OXYGEN; FIRST- AND SECOND-ORDER REACTIONS OF THE ORGANIC PEROXYL RADICALS; THE ROLE OF ISOPYRIMIDINES AS INTERMEDIATES

Al-Sheikhly, Mohamed I.,Hissung, Alfred,Schuchmann, Heinz-Peter,Schuchmann, Man Nien,Sonntag, Clemens von,et al.

, p. 601 - 608 (2007/10/02)

The nature and yields of the products of radiolysis of aqueous solutions of dihydrouracil containing both N2O and O2 strongly depend on pH and dose rate.At a dose rate of 0.3 Gy s-1 and at pH 3, the major products are barbituric acid (G 2.4), labile material (G 2.8), and uracil (G 0.1).The labile material is converted into uracil upon treatment with acid and is largely composed of 5,6-dihydro-6-hydroxyuracil.At pH 7 barbituric acid is absent and uracil becomes the major product (G 4.5); some labile material is also formed (G 0.7).At pH 5 the pattern of the product distribution changes as a function of dose rate.With increasing dose r ate G(uracil) decreases whereas G(barbituric acid) increases.The predominant radical formed in the dihydrouracil system is the 6-peroxyl radical, and it has been found, using pulse radiolysis with both optical and conductometric detection, that this peroxyl radical can eliminate O2-. to give uracil via an unstable isomeric form of the pyrimidine (isouracil).The elimination is base-catalysed so that, under alkaline conditions, uracil is the major radiolysis product.At lower pH, and also at higher dose rates, bimolecular decay of the peroxyl radical competes with the O2-. elimination process, barbituric acid being a specific product of the bimolecular decay route.The mechanism of these processes are discussed.Irradiation of dihydrothymine-N2O-O2 solutions gave similar results.

EFFECT OF COPPER(II) IONS ON THE γ-RADIOLYSIS OF URACIL

Bhattacharyya, Sudhindra N.,Mandal, Parikshit C.

, p. 2613 - 2630 (2007/10/02)

Radiation sensitization of uracil (Ura) by CuII ions has been investigated using cobalt-60 γ-rays.In N2O-saturated solution, when no additive is present, the base degradation yield, G(-Ura), is only ca. 3.3, but when CuII ions are added in either a free or complexed state to the solution before irradiation, G(-Ura) is found to increase to ca. 5.1.The enhanced degradation of the base is derived from the oxidized transient, e.g.UraOH+, although reduction of CuII to CuI has been ascribed to all the primary adducts, e.g.UraH, UraOH and Ura-.Glycol and isobarbituric acid constitute the major products of radiolysis, which are derived from the oxidized UraOH+ species.Hydroxydihydrouracil and its dimer have also been detected in significant yields when the radiolysis is carried out at comparitively high absorbed doses.The formation of these products has been ascribed to a secondary reaction between UraOH and CuI which proceeds through the intermediate formation of a Cu-C bond.

Analysis of Radiolysis Products of Aqueous Uracil + N2O Solutions

Ali, Khondoker M. Idris,Scholes, George

, p. 449 - 456 (2007/10/02)

Various products from the irradiation of solutions of uracil+N2O with 60Co gamma rays were separated by paper chromatographic technique using 14C labelled materials.Identity of the isolated products was investigated by spectrophotometric and kinetic decomposition studies.Thus at least eight radiolytic products of uracil such as cis- and trans-uracil glycols, 5-hydroxy-6-hydro and 6-hydroxy-5-hydro compounds, isobarbituric acid and three dimeric products were identified.Yields of these products were determined at different pH values; a good material mass balance was achieved; the mechanism involved is discussed.

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