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Uridine, 5-(4-aminophenyl)-2'-deoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

108664-87-5

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108664-87-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108664-87-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,6,6 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 108664-87:
(8*1)+(7*0)+(6*8)+(5*6)+(4*6)+(3*4)+(2*8)+(1*7)=145
145 % 10 = 5
So 108664-87-5 is a valid CAS Registry Number.

108664-87-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(p-aminophenyl)-2'-deoxyuridine

1.2 Other means of identification

Product number -
Other names 5-(4-Amino-phenyl)-1-((2R,4S,5R)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-1H-pyrimidine-2,4-dione

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:108664-87-5 SDS

108664-87-5Downstream Products

108664-87-5Relevant academic research and scientific papers

Linear Free Energy Relationship Studies of 5-Substituted 2,4-Dioxopyrimidine Nucleosides

Chang, George,Mertes, Mathias P.

, p. 3625 - 3631 (2007/10/02)

The development of a direct and efficient palladium(0)-catalyzed biaryl coupling reaction permitted the synthesis of a series of N1-substituted 5-aryl-2,4-dioxopyrimidines.The physical and spectral properties of these compounds were determined and correlated by various linear free energy relationships.The relationships between the physical and spectral data with Hammett ? constants proved useful in analyzing the electron distribution of the heterocycle.Although a significant degree of orbital overlap and interaction between the substituents and the pyrimidine ring was observed, it is doubtful that the interactions are comparable to those of a benzene ring system.

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