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5-FLUORODIHYDRO-6-HYDROXY-2,4-(1H,3H)-PYRIMIDINEDIONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37103-91-6

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37103-91-6 Usage

Chemical Properties

Pale Pink Solid

Uses

An impurity of 5-Fluorouracil (F596000).

Check Digit Verification of cas no

The CAS Registry Mumber 37103-91-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,1,0 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 37103-91:
(7*3)+(6*7)+(5*1)+(4*0)+(3*3)+(2*9)+(1*1)=96
96 % 10 = 6
So 37103-91-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H5FN2O3/c5-1-2(8)6-4(10)7-3(1)9/h1-2,8H,(H2,6,7,9,10)

37103-91-6SDS

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-fluoro-6-hydroxy-1,3-diazinane-2,4-dione

1.2 Other means of identification

Product number -
Other names 5-Fluor-6-hydroxydihydrouracil

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:37103-91-6 SDS

37103-91-6Downstream Products

37103-91-6Relevant academic research and scientific papers

Photochemical reactions of 5-fluoropyrimidine bases with selected alkylamines

Kanciurzewska, Anna,Raczkowski, Mateusz,Ciszewski, Krzysztof,Celewicz, Lech

, p. 761 - 763 (2003)

Novel photochemical reactions between 5-fluoropyrimidine bases and primary alkylamines are described. Photoreaction of 5-fluorouracil with alkylamines in aqueous solution (pH>8) leads to 5-alkylaminouracils as the main photoproducts. Similarly, photoreact

Glorination of Pyrimidines. Part 2. Mechanistic Aspects of the Reaction of Acetyl Hypofluorite with Uracil and Cytosine Derivatives

Visser, W. M. Gerard,Herder, E. Renella,Kanter, Frans J. J. de,Herscheid D. M. Jacobus

, p. 1203 - 1208 (2007/10/02)

The reaction of acetyl hypofluorite (AcOF) with uracil, cytosine, and some N-1-substituted derivatives dissolved in either acetic acid or water has been investigated.Analysis by radio-h.p.l.c., using (18)f as a tracer, and by (1)H n.m.r. revealed that a substituent at N-1 of uracil has a remarkable effect on the stability of the intermediate 6-acetoxy-5-fluoro-5,6-dihydrouracils.In addition, it was found that these cytosine adducts rapidly deaminate in water yielding their corresponding uracil analogues.

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