84394-36-5 Usage
Uses
Used in Pharmaceutical Industry:
(3R,4R)-2,2-dimethyl-3-phenyl-4-[4-(2-pyrrolidin-1-ylethoxy)phenyl]-3,4-dihydro-2H-chromen-7-ol is used as a potential therapeutic agent for various medical conditions due to its unique structure and potential biological activities.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (3R,4R)-2,2-dimethyl-3-phenyl-4-[4-(2-pyrrolidin-1-ylethoxy)phenyl]-3,4-dihydro-2H-chromen-7-ol is used as a starting point for the development of new drugs. Its specific stereochemistry and functional groups make it an interesting candidate for further research and modification to enhance its pharmacological properties.
Used in Drug Delivery Systems:
Similar to gallotannin, (3R,4R)-2,2-dimethyl-3-phenyl-4-[4-(2-pyrrolidin-1-ylethoxy)phenyl]-3,4-dihydro-2H-chromen-7-ol may also be employed in the development of novel drug delivery systems to improve its bioavailability and therapeutic outcomes. Organic and metallic nanoparticles could be utilized as carriers for (3R,4R)-2,2-dimethyl-3-phenyl-4-[4-(2-pyrrolidin-1-ylethoxy)phenyl]-3,4-dihydro-2H-chromen-7-ol, aiming to enhance its delivery and efficacy in targeted applications.
Check Digit Verification of cas no
The CAS Registry Mumber 84394-36-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,3,9 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 84394-36:
(7*8)+(6*4)+(5*3)+(4*9)+(3*4)+(2*3)+(1*6)=155
155 % 10 = 5
So 84394-36-5 is a valid CAS Registry Number.
84394-36-5Relevant academic research and scientific papers
A facile synthesis of a 3,4-trans-7-hydroxy-2,2-dimethyl-3-phenyl-4-(p-pyrrolidinoethoxyphenyl)chroman
Srivastava, Apurva K.,Lal, J.,Gupta, R. C.,Grover, P. K.
, p. 773 - 774 (2007/10/02)
cis-Centchroman (6) on treatment with hydrazine hydrate, ethylene glycol and potassium hydroxide under oxygen-free nitrogen atmosphere at 230-240 deg C, undergoes both dealkylation and isomerization reactions giving rise to desmethylcentchroman (1) and 3,
