56865-97-5 Usage
Uses
Used in Organic Synthesis:
2,5-Dihydroxybenzylamine is used as a building block in organic synthesis for the production of other compounds. Its unique structure with two hydroxyl groups allows for various chemical reactions, making it a valuable component in creating a wide array of chemical products.
Used in Chemical Research:
In the realm of chemical research, 2,5-dihydroxybenzylamine serves as an important compound for studying the properties and reactions of hydroxyl-substituted benzene derivatives. Its presence in research contributes to the advancement of knowledge in organic chemistry and related fields.
Used in Pharmaceutical and Drug Development:
2,5-Dihydroxybenzylamine is used as a potential therapeutic agent in the pharmaceutical industry. Its unique chemical structure may offer novel avenues for drug development, particularly in the creation of new medications with specific therapeutic targets.
Used in Various Industries:
Given its versatility, 2,5-dihydroxybenzylamine has potential applications across different industries. Its use may extend to areas such as material science, where it could be employed in the development of new materials with specific properties, or in the agrochemical sector for the synthesis of active ingredients in pesticides or fertilizers.
Check Digit Verification of cas no
The CAS Registry Mumber 56865-97-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,6 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56865-97:
(7*5)+(6*6)+(5*8)+(4*6)+(3*5)+(2*9)+(1*7)=175
175 % 10 = 5
So 56865-97-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO2/c8-4-5-3-6(9)1-2-7(5)10/h1-3,9-10H,4,8H2
56865-97-5Relevant academic research and scientific papers
Synthesis of novel 1,4-benzoquinone-containing 1,2,3-triazoles: An entry into a new library
Algi, Fatih,Balci, Metin
experimental part, p. 1341 - 1347 (2009/12/07)
A heretofore unexplored library of 1,4-benzoquinone-containing 1,2,3-triazoles was prepared by the application of a highly regioselective copper(I)-catalyzed process. Furthermore, the utilization of this novel triazole-1,4-benzoquinone system as an intere
