38228-20-5 Usage
Description
[[4-amino-6-[(hydroxymethyl)amino]-1,3,5-triazin-2-yl]imino]bismethanol, also known as bismethanol, is a chemical compound derived from 1,3,5-triazine with a unique molecular structure. It features an amino group, a hydroxymethyl group, and two methanol groups, which provide a variety of functional groups for potential chemical reactions. This versatile compound serves as a valuable building block in the development of new materials and pharmaceutical products.
Uses
Used in Organic Synthesis:
[[4-amino-6-[(hydroxymethyl)amino]-1,3,5-triazin-2-yl]imino]bismethanol is used as a reagent in organic synthesis for the preparation of novel compounds. Its diverse functional groups allow for a wide range of chemical reactions, making it a valuable asset in the creation of new molecules with specific properties and applications.
Used in Pharmaceutical Development:
In the pharmaceutical industry, [[4-amino-6-[(hydroxymethyl)amino]-1,3,5-triazin-2-yl]imino]bismethanol is used as a building block for the development of new drugs. Its unique molecular structure and functional groups can be utilized to create innovative pharmaceutical products with potential therapeutic benefits.
Used in Material Science:
[[4-amino-6-[(hydroxymethyl)amino]-1,3,5-triazin-2-yl]imino]bismethanol is also employed in material science as a versatile building block for the development of new materials. Its structure and properties can be harnessed to create materials with specific characteristics, such as improved strength, durability, or chemical resistance, depending on the desired application.
Check Digit Verification of cas no
The CAS Registry Mumber 38228-20-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,2 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 38228-20:
(7*3)+(6*8)+(5*2)+(4*2)+(3*8)+(2*2)+(1*0)=115
115 % 10 = 5
So 38228-20-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H12N6O3/c7-4-9-5(8-1-13)11-6(10-4)12(2-14)3-15/h13-15H,1-3H2,(H3,7,8,9,10,11)
38228-20-5Relevant articles and documents
Canonical Chemical Theories Exemplified by the Mehtylolation of Urea and Melamine
Gebregiorgis, Taddesse,Gordon, Manfred
, p. 359 - 382 (2007/10/02)
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.
