183551-83-9 Usage
Uses
Used in Organic Synthesis:
Naphtho[2,1-b]furan-6(7H)-one, 8,9-dihydro-1,5,8-trimethyl-, (8S)is used as a key intermediate in organic synthesis for the preparation of various complex organic molecules. Its unique structure and functional groups make it a valuable building block for the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Research:
Due to its structural features and potential biological activities, Naphtho[2,1-b]furan-6(7H)-one, 8,9-dihydro-1,5,8-trimethyl-, (8S)is used as a starting material in the development of new pharmaceutical agents. Its furan ring and ketone group can be further modified to explore its potential as a therapeutic agent for various diseases.
Used in Material Science Research:
Naphtho[2,1-b]furan-6(7H)-one, 8,9-dihydro-1,5,8-trimethyl-, (8S)is also used in material science research to investigate its properties and potential applications in the development of new materials. Its unique structure and stereochemistry may contribute to the creation of novel materials with specific properties, such as optical, electronic, or mechanical characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 183551-83-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,5,5 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 183551-83:
(8*1)+(7*8)+(6*3)+(5*5)+(4*5)+(3*1)+(2*8)+(1*3)=149
149 % 10 = 9
So 183551-83-9 is a valid CAS Registry Number.
183551-83-9Relevant academic research and scientific papers
Santoro, Stefano,Superchi, Stefano,Messina, Federica,Santoro, Ernesto,Rosati, Ornelio,Santi, Claudio,Marcotullio, M. Carla
, p. 1254 - 1259 (2013)
Agarsenone (1), a new cadinane sesquiterpenoid, was isolated from the resin of Commiphora erythraea. The structures of 1 and its decomposition products agarsenolides (2a and 2b) and myrrhone (3) were established by extensive NMR spectroscopic analysis. The absolute configuration of 3 and the relative and absolute configurations of 1 were assigned by comparison of experimental and calculated optical rotatory dispersion and electronic circular dichroism spectra.
