87656-34-6 Usage
Uses
Used in Organic Chemistry:
(9,10-dihydro-9,10-[1,2]benzenoanthracen-9-yl)sulfanol is used as a synthetic intermediate for the creation of various organic compounds. Its specific structure allows for versatile chemical reactions, making it a valuable building block in the synthesis of a wide range of molecules.
Used in Materials Science:
In the field of materials science, (9,10-dihydro-9,10-[1,2]benzenoanthracen-9-yl)sulfanol is used as a component in the development of functional materials. Its unique chemical structure contributes to the properties of these materials, potentially enhancing their performance in various applications.
Used in Pharmaceutical Research:
Due to its distinctive chemical features, (9,10-dihydro-9,10-[1,2]benzenoanthracen-9-yl)sulfanol may be utilized in pharmaceutical research as a starting point for the design and development of new drugs. Its interaction with biological systems could lead to the discovery of novel therapeutic agents.
Used in Biological Research:
In biological research, (9,10-dihydro-9,10-[1,2]benzenoanthracen-9-yl)sulfanol may serve as a probe or tool to study the interactions between small molecules and biological targets. Its unique structure could provide insights into various biological processes and contribute to the understanding of complex biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 87656-34-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,5 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 87656-34:
(7*8)+(6*7)+(5*6)+(4*5)+(3*6)+(2*3)+(1*4)=176
176 % 10 = 6
So 87656-34-6 is a valid CAS Registry Number.
87656-34-6Relevant academic research and scientific papers
The redox chemistry of sulfenic acids
McGrath, Alaina J.,Garrett, Graham E.,Valgimigli, Luca,Pratt, Derek A.
supporting information; experimental part, p. 16759 - 16761 (2011/02/17)
A persistent triptycenyl sulfenic acid is used as a model for cysteine-derived and other biologically relevant sulfenic acids in experiments which define their redox chemistry. EPR spectroscopy reveals that sulfinyl radicals are persistent and unreactive toward O2, allowing the O-H bonding dissociation enthalpy (BDE) of the sulfenic acid to be readily determined by equilibration with TEMPO as 71.9 kcal/mol. The E° (RSO/RSO-) and pKa of this sulfenic acid are also reported.
THIO- AND OXO-ACIDS OF TRICOORDINATED SULFUR: SYNTHETIC AND STEREOCHEMICAL ASPECTS
Drabowicz, Jozef,Lyzwa, Piotr,Bujnicki, Bogdan,Mikolajczyk, Marian
, p. 293 - 312 (2007/10/02)
This account describes the first synthesis, characterization and reactivity of the relatively stable thiosulfinic acid salts.New approaches for the preparation of optically active sulfinic acid salts and sulfones, which are chiral due to 16O, 18O isotopic substitution, as well as measurement of their chirooptical properties are also presented.Key words: thiosulfinic acid salts, chiral 16O, 18O-sulfinic acids salts, sulfinyl chlorides, optically active sulfoxides, optically active 16O, 18O-sulfones, optical activity, circular dichroism.
