70628-26-1 Usage
Structure
Cyclic urea derivative with a furan ring
Common uses
Pharmaceutical intermediate, corrosion inhibitor
Potential antitumor activity
Being studied for medicinal properties
Application in corrosion prevention
Investigated for use in the oil and gas industry for metallic materials
Versatility
Various potential applications in pharmaceuticals and industrial processes
Check Digit Verification of cas no
The CAS Registry Mumber 70628-26-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,2 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 70628-26:
(7*7)+(6*0)+(5*6)+(4*2)+(3*8)+(2*2)+(1*6)=121
121 % 10 = 1
So 70628-26-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2O2/c1-10(2)8(11)9-6-7-4-3-5-12-7/h3-5H,6H2,1-2H3,(H,9,11)
70628-26-1Relevant articles and documents
Synthesis of N -Acyl-5-aminopenta-2,4-dienals via base-induced ring-opening of N -acylated furfurylamines: Scope and limitations
Ouairy, Cecile,Michel, Patrick,Delpech, Bernard,Crich, David,Marazano, Christian
supporting information; experimental part, p. 4311 - 4314 (2010/09/04)
N-Acylation of furfurylamines provided 1, which on double deprotonation with LDA led to the formation of N-acyl-5-aminopenta-2,4-dienals 2 via an isomerization involving opening of the furan ring. The scope and limitations of the procedure were examined by considering the influence of substituents on the carbonyl group and also on the heterocycle moiety. The efficacy of the reaction was shown to be very dependent on the nature of these groups.
