745784-01-4 Usage
Description
(R)-(+)-1-(4-BROMOPHENYL)ETHYL ISOTHIOCYANATE, with the molecular formula C10H9BrNS, is an isothiocyanate derivative known for its diverse biological activities. This chemical compound is characterized by its ability to bind with a variety of molecules, making it a versatile compound in the fields of organic synthesis and chemical reactions. Its potential pharmacological properties, particularly as an anticancer agent, have garnered significant interest, along with its possible use in the development of new drugs and pharmaceuticals.
Uses
Used in Organic Synthesis:
(R)-(+)-1-(4-BROMOPHENYL)ETHYL ISOTHIOCYANATE is used as a reagent in organic synthesis for its ability to bind with a variety of molecules, facilitating the creation of new compounds and contributing to the advancement of chemical research.
Used in Chemical Reactions:
In the field of chemical reactions, (R)-(+)-1-(4-BROMOPHENYL)ETHYL ISOTHIOCYANATE is used as a versatile compound that can participate in various reactions, enhancing the understanding of chemical processes and potentially leading to the discovery of novel chemical entities.
Used in Pharmaceutical Research:
(R)-(+)-1-(4-BROMOPHENYL)ETHYL ISOTHIOCYANATE is used as a compound of interest in pharmaceutical research for its potential pharmacological properties, including its potential as an anticancer agent. Its ability to bind with various molecules makes it a promising candidate for the development of new drugs and pharmaceuticals.
Used in Anticancer Applications:
In the medical field, (R)-(+)-1-(4-BROMOPHENYL)ETHYL ISOTHIOCYANATE is being studied for its potential as an anticancer agent, with the aim of developing new treatments for various types of cancer. Its diverse biological activities and molecular binding capabilities make it a valuable compound in the search for effective cancer therapies.
Used in Drug Development:
(R)-(+)-1-(4-BROMOPHENYL)ETHYL ISOTHIOCYANATE is also used in the development of new drugs and pharmaceuticals, leveraging its unique properties to create innovative and effective treatments for a range of medical conditions. Its potential applications in this area are still being explored, but its versatility and biological activities make it a promising compound for future drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 745784-01-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,5,7,8 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 745784-01:
(8*7)+(7*4)+(6*5)+(5*7)+(4*8)+(3*4)+(2*0)+(1*1)=194
194 % 10 = 4
So 745784-01-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H8BrNS/c1-7(11-6-12)8-2-4-9(10)5-3-8/h2-5,7H,1H3/t7-/m1/s1