6588-68-7 Usage
Description
3,5-DiMethyl-1-nitroadaMantane, also known as 1,3-Dimethyl-5-nitroadamantane, is an organic compound with a unique molecular structure characterized by two methyl groups and a nitro group attached to an adamantane core. It is known for its potential neuroprotective properties and is being explored for its therapeutic applications in various medical fields.
Uses
Used in Pharmaceutical Industry:
3,5-DiMethyl-1-nitroadaMantane is used as a neuroprotective agent for the treatment of neurodegenerative disorders such as Parkinson's disease. Its neuroprotective properties make it a promising candidate for mitigating the progression of these disorders and improving the quality of life for patients.
Used in Neurodegenerative Disorder Treatment:
3,5-DiMethyl-1-nitroadaMantane is used as a therapeutic agent for the treatment of neurodegenerative disorders, particularly Parkinson's disease. It is believed to aid in the protection and preservation of neurons, potentially slowing down the progression of the disease and providing relief from its symptoms.
Check Digit Verification of cas no
The CAS Registry Mumber 6588-68-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,8 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6588-68:
(6*6)+(5*5)+(4*8)+(3*8)+(2*6)+(1*8)=137
137 % 10 = 7
So 6588-68-7 is a valid CAS Registry Number.
6588-68-7Relevant articles and documents
Selective Nitroxylation of Adamantane Derivatives in the System Nitric Acid–Acetic Anhydride
Ivleva, E. A.,Klimochkin, Yu. N.,Moiseev, I. K.
, p. 1532 - 1539 (2020/10/22)
Abstract: A number of new nitroxyadamantanes have been synthesized by nitroxylation of the corresponding substrates with nitric acid in acetic anhydride. High electrophilicity and reduced acidity of the system HNO3–Ac2O increases the stability of nitrates and significantly decreases the probability of formation of alcohols. In some cases, nitrolysis and oxidation of functional groups in the substrate are observed.
[VO(H2O)5]H[PMo12O40]- catalyzed nitration of alkanes with nitric acid
Yamaguchi, Kazuya,Shinachi, Satoshi,Mizuno, Noritaka
, p. 424 - 425 (2007/10/03)
[VO(H2O)5]H[PMo12O40], which contains vanadyl counter cations and PMo12O40 3-, can act as a catalyst for the nitration of various alkanes including alkylbenzenes using nitric acid as a nitrating agent in acetic acid at 356 K.
Efficient Catalytic Alkane Nitration with NO2 under Air Assisted by N-Hydroxyphthalimide
Sakaguchi, Satoshi,Nishiwaki, Yoshiki,Kitamura, Takaaki,Ishii, Yasutaka
, p. 222 - 224 (2007/10/03)
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