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100814-60-6

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100814-60-6 Usage

General Description

2(1H)-Pyrimidinone,4-amino-5-fluoro-5,6-dihydro-6-hydroxy-,trans-(9CI) is a chemical compound with the molecular formula C4H5FN2O2. It is a heterocyclic organic compound with a pyrimidine ring structure, containing an amino group at the 4-position and a fluorine atom at the 5-position. The trans configuration refers to the relative positioning of the substituents on the pyrimidine ring. 2(1H)-Pyrimidinone,4-amino-5-fluoro-5,6-dihydro-6-hydroxy-,trans-(9CI) may have potential biological activity or pharmaceutical applications, and further research on its properties and uses may be warranted.

Check Digit Verification of cas no

The CAS Registry Mumber 100814-60-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,8,1 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 100814-60:
(8*1)+(7*0)+(6*0)+(5*8)+(4*1)+(3*4)+(2*6)+(1*0)=76
76 % 10 = 6
So 100814-60-6 is a valid CAS Registry Number.

100814-60-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name (4S,5R)-5-Fluoro-4-hydroxy-6-imino-tetrahydro-pyrimidin-2-one

1.2 Other means of identification

Product number -
Other names -

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:100814-60-6 SDS

100814-60-6Downstream Products

100814-60-6Relevant articles and documents

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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