135439-46-2 Usage
Heterocyclic compound
Yes
It contains a phosphorus atom and a five-membered ring with two nitrogen atoms, making it a heterocyclic compound.
Chiral ligand
Yes
It is used in organic synthesis as a chiral ligand in asymmetric catalysis, which is important for the production of enantiomerically pure compounds.
Potential applications
Pharmaceutical industry
The compound has potential applications in the pharmaceutical industry for the production of various drugs and biologically active compounds due to its unique structural and chemical properties.
Anticancer and antiviral activities
Studied
It has been studied for its potential anticancer and antiviral activities, although further research is required to fully understand and harness these potential benefits.
Further research needed
Yes
More research and studies are necessary to fully understand the compound's properties, potential benefits, and applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 135439-46-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,4,3 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 135439-46:
(8*1)+(7*3)+(6*5)+(5*4)+(4*3)+(3*9)+(2*4)+(1*6)=132
132 % 10 = 2
So 135439-46-2 is a valid CAS Registry Number.
135439-46-2Relevant articles and documents
Phosphoric amides. Part 11. Intramolecular reactivity of phosphorotriamidates
Bauermeister, Siegelinde,Modro, Agnes M.,Modro, Tom A.,Zwierzak, Andrzej
, p. 811 - 816 (2007/10/02)
Five N-(2-chloroethyl)phosphorotriamidates, (RNH)2P(O)NHCH2CH2Cl, have been synthesized, and their behavior under strongly basic conditions was studied.For N-alkyl derivatives (R = Me, PhCH2), base-promoted intramolecular displacement of chloride yielded the N-phosphorylated aziridine, (RNH)2P(O)NC2H4, as the exclusive cyclization product.For N-aryl derivatives (R = Ar), both the aziridine and the 1,3,2-diazaphospholidine, RNHP(O)NHCH2CH2NR, products could be obtained in comparable yields.The N-aromatic cyclic products are mutually interconvertible; 1,3,2-diazaphospholidines rearrange to the corresponding aziridines upon treatment with base, while bromide ions catalyze the reverse isomerization. Key words: phosphoramidates acidity, N-phosphorylated aziridines - 1,3,2-diazaphospholidines isomerization, 1,3 vs. 1,5 cyclization.
