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100814-57-1

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100814-57-1 Usage

Chemical Class

Pyrimidinone

Heterocyclic compound

Yes

Contains

Different sources of media describe the Contains of 100814-57-1 differently. You can refer to the following data:
1. Pyrimidine ring
2. Fluorine atom
3. Amino group

Configuration

cis

Functional groups location

Same side of the molecule

Potential applications

Pharmaceuticals

Biological activity

Possible

Further research needed

Yes

Check Digit Verification of cas no

The CAS Registry Mumber 100814-57-1 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, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 100814-57:
(8*1)+(7*0)+(6*0)+(5*8)+(4*1)+(3*4)+(2*5)+(1*7)=81
81 % 10 = 1
So 100814-57-1 is a valid CAS Registry Number.

100814-57-1SDS

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 (4R,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:100814-57-1 SDS

100814-57-1Downstream Products

100814-57-1Relevant 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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