70443-38-8 Usage
Description
(3S,4S)-1,2,3,4-tetrahydrobenzo[k]tetraphene-3,4-diol is a complex chiral chemical compound characterized by a four-ring benzene structure, also known as a tetraphene, connected to a diol functional group. This molecule is classified as chiral due to its two stereocenters at the 3S and 4S positions. The diol functional group suggests that it is an alcohol compound. Its intricate molecular structure and chiral nature may endow it with distinct chemical and physical properties, making it a valuable candidate for research and potential applications across various sectors, including pharmaceuticals, materials science, and organic chemistry.
Uses
Used in Pharmaceutical Applications:
(3S,4S)-1,2,3,4-tetrahydrobenzo[k]tetraphene-3,4-diol is used as a pharmaceutical compound for its potential therapeutic effects. Given its complex structure and chiral nature, it may interact with biological targets in unique ways, offering novel avenues for drug development and treatment of various diseases.
Used in Materials Science:
In the field of materials science, (3S,4S)-1,2,3,4-tetrahydrobenzo[k]tetraphene-3,4-diol is used as a component in the development of new materials. Its unique molecular structure and properties may contribute to the creation of advanced materials with specific characteristics, such as improved strength, flexibility, or chemical resistance.
Used in Organic Chemistry Research:
(3S,4S)-1,2,3,4-tetrahydrobenzo[k]tetraphene-3,4-diol serves as a valuable compound in organic chemistry research. Its complex structure and chirality make it an interesting subject for studying reaction mechanisms, stereochemistry, and the development of new synthetic methods or catalysts.
Used in Chemical Synthesis:
As a chiral molecule with a unique structure, (3S,4S)-1,2,3,4-tetrahydrobenzo[k]tetraphene-3,4-diol is used as a key intermediate or building block in the synthesis of other complex organic compounds. Its specific stereochemistry can be exploited to control the outcome of chemical reactions, leading to the production of enantiomerically pure compounds with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 70443-38-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,4,4 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 70443-38:
(7*7)+(6*0)+(5*4)+(4*4)+(3*3)+(2*3)+(1*8)=108
108 % 10 = 8
So 70443-38-8 is a valid CAS Registry Number.
70443-38-8Relevant articles and documents
Synthesis and isomerization of arene oxide metabolites of phenanthrene, triphenylene, dibenz[a,c]anthracene and dibenz[a,h]anthracene
Balani,Brannigan,Boyd,Sharma,Hempenstall,Smith
, p. 1091 - 1097 (2007/10/03)
Dibenz[a,h]anthracene 3,4-oxide 5ARS, synthesised from the enantiopure dibromoMTPA precursor 9ARRS*, was found to have totally racemized and to be accompanied by benz[5,6]anthra[1,2-b]oxepine 11A. Phenanthrene 3,4-oxide 5BRS/su
