31962-32-0 Usage
Uses
Used in Organic Synthesis:
[(4,6-diamino-1,3,5-triazin-2-yl)imino]bismethanol is used as a building block for the synthesis of various organic compounds due to its reactive amino and hydroxyl groups, which can participate in a range of chemical reactions, such as condensation, substitution, and addition reactions.
Used in Materials Science:
In the field of materials science, [(4,6-diamino-1,3,5-triazin-2-yl)imino]bismethanol is used as a precursor for the development of novel materials with specific properties. Its unique structure allows for the creation of materials with tailored characteristics, such as improved stability, reactivity, or selectivity.
Used in Pharmaceutical Research:
[(4,6-diamino-1,3,5-triazin-2-yl)imino]bismethanol is being studied for its potential biological activities and pharmacological properties. Its chemical structure makes it an interesting candidate for the development of new drugs, particularly in areas where its amino and hydroxyl groups can be exploited for interactions with biological targets.
Used in Chemical Research:
As a compound with a distinct structure, [(4,6-diamino-1,3,5-triazin-2-yl)imino]bismethanol is used in chemical research to understand its reactivity, stability, and the potential for new reactions or mechanisms. This knowledge can lead to the discovery of new chemical processes or the improvement of existing ones.
Check Digit Verification of cas no
The CAS Registry Mumber 31962-32-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,9,6 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 31962-32:
(7*3)+(6*1)+(5*9)+(4*6)+(3*2)+(2*3)+(1*2)=110
110 % 10 = 0
So 31962-32-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H10N6O2/c6-3-8-4(7)10-5(9-3)11(1-12)2-13/h12-13H,1-2H2,(H4,6,7,8,9,10)
31962-32-0Relevant academic research and scientific papers
Gebregiorgis, Taddesse,Gordon, Manfred
, p. 359 - 382 (1984)
Old and recent data on equilibria and kinetics of methylolation of urea and melamine are analysed.The theoretical framework affords a sequence, claimed to be canonical of successive phenomenological approximations.The theory, expounded earlier, begin with two successive schemes whose essentials go back to early work by Pauling and by Flory.The two stages here suffice to show that all the data from eight laboratories, covering the six-membered family of methylol ureas and rhe ten-membered family of methylol melamines, are in quantitative agreement, a circumstance unsespected by other workers in the field.The statisticalthermodynamic and kinetic principles involved are therefore expounded in more detail than before.Using them, very small substituent effects (e.g O.35 kJ kol-1 are deduced with high significance and accuracy.Owing largly to the recent measurement by Tomita, the methylol melamines are claimed currently to be the thermdinamically best characterised family in the chemical literature.A challenge arises for theoretical chemists to test quantum-theoreticaltechniques against the measured energetics of substituent effects in this family, and to exploit for other families the graph-theoretical analysis of molecular additivity which underlies the approximation schemes, which already well tested.
