701-68-8 Usage
Uses
Used in Pharmaceutical Research and Development:
3,5-DIBROMO-4-HYDROXYBENZYLAMINE is used as a building block in the synthesis of new drugs and pharmaceuticals, leveraging its structural properties and reactivity to create novel compounds with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 3,5-DIBROMO-4-HYDROXYBENZYLAMINE is utilized as a key intermediate for the creation of various organic compounds, contributing to the development of new chemical entities with diverse applications.
Used in Antimicrobial and Antifungal Agents Development:
3,5-DIBROMO-4-HYDROXYBENZYLAMINE is studied for its antimicrobial and antifungal properties, making it a candidate for the development of new antimicrobial agents to combat resistant strains and improve public health.
Used in Medicinal Chemistry Research:
Due to its potential biological activities and unique structure, 3,5-DIBROMO-4-HYDROXYBENZYLAMINE is employed in medicinal chemistry research to explore its therapeutic potential and to understand its mechanisms of action, which could lead to the discovery of new treatments and interventions in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 701-68-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 701-68:
(5*7)+(4*0)+(3*1)+(2*6)+(1*8)=58
58 % 10 = 8
So 701-68-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H7Br2NO/c8-5-1-4(3-10)2-6(9)7(5)11/h1-2,11H,3,10H2
701-68-8Relevant academic research and scientific papers
Improved Stabilities of Labeling Probes for the Selective Modification of Endogenous Proteins in Living Cells and In Vivo
Lin, Kuan-Yu,Hin Lam, Chak,Lin, Xin-Hui,Hsu, Jung-I,Fan, Syuan-Yun,Gupta, Nitesh K.,Lin, Yu-Chun,Khoon Tee, Boon,Li, Jui-Ping,Chen, Jen-Kun,Tan, Kui-Thong
, p. 937 - 948 (2021/03/16)
To date, various affinity-based protein labeling probes have been developed and applied in biological research to modify endogenous proteins in cell lysates and on the cell surface. However, the reactive groups on the labeling probes are also the cause of
