885965-71-9 Usage
Derivative of acetamidine
The compound is derived from acetamidine, which is a chemical compound with the formula NH2-CH2-CONH2.
Used in synthesis of pharmaceuticals and agrochemicals
The compound is commonly used as a building block in the synthesis of other chemicals, including pharmaceuticals and agrochemicals.
Two fluorine atoms attached to a phenyl ring
The presence of two fluorine atoms attached to a phenyl ring gives the compound unique chemical properties and makes it a valuable building block in organic chemistry.
Heterocyclic compound
The compound is classified as a heterocyclic compound, meaning it contains a ring of atoms with at least one nitrogen atom.
Potential applications in drug discovery and development
The compound has potential applications in drug discovery and development due to its ability to form versatile chemical bonds and its pharmacological properties.
Presence of acetamidine functional group
The presence of the acetamidine functional group makes the compound a potential candidate for the development of new antiviral and antibacterial agents.
Check Digit Verification of cas no
The CAS Registry Mumber 885965-71-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,9,6 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 885965-71:
(8*8)+(7*8)+(6*5)+(5*9)+(4*6)+(3*5)+(2*7)+(1*1)=249
249 % 10 = 9
So 885965-71-9 is a valid CAS Registry Number.
885965-71-9Relevant articles and documents
Evolution of anti-HIV drug candidates. Part 1: From α-Anilinophenylacetamide (α-APA) to imidoyl thiourea (ITU)
Ludovici, Donald W.,Kukla, Michael J.,Grous, Philip G.,Krishnan, Suma,Andries, Koen,De Bethune, Marie-Pierre,Azijn, Hilde,Pauwels, Rudi,De Clercq, Erik,Arnold, Edward,Janssen, Paul A.J.
, p. 2225 - 2228 (2007/10/03)
Stemming from work on a previous clinical candidate, loviride, and other α-APA derivatives, a new series of potent non-nucleoside reverse transcriptase inhibitors (NNRTIs) has been synthesized. The ITU analogues, which contain a unique diarylated imidoyl thiourea, are very active in inhibiting both wild-type and clinically important mutant strains of HIV-1.
