101990-65-2 Usage
Uses
Used in Pharmaceutical Synthesis:
(6-(methylthio)pyridin-3-yl)methanol is used as a key intermediate in the synthesis of various pharmaceuticals and organic compounds. Its unique chemical structure allows for the creation of a wide range of molecules with diverse therapeutic applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (6-(methylthio)pyridin-3-yl)methanol is used as a building block for designing and developing new drugs. Its antioxidant and anti-cancer properties make it a promising candidate for the treatment of various diseases, including cancer.
Used in Drug Development:
(6-(methylthio)pyridin-3-yl)methanol is utilized in drug development to explore its potential as a therapeutic agent. Its biological activities, such as antioxidant and anti-cancer properties, are being investigated to determine its efficacy and safety in treating specific health conditions.
Used in Chemical Research:
(6-(methylthio)pyridin-3-yl)methanol serves as a valuable research tool in the field of chemistry. Its unique structure and properties make it an interesting subject for studying various chemical reactions and mechanisms, contributing to the advancement of chemical knowledge and technology.
Used in Antioxidant Applications:
(6-(methylthio)pyridin-3-yl)methanol is used as an antioxidant in various industries, including the food and cosmetics industries. Its ability to neutralize free radicals and protect cells from oxidative damage makes it a valuable additive for preserving the quality and shelf life of products.
Used in Cancer Research:
In cancer research, (6-(methylthio)pyridin-3-yl)methanol is used as a potential anti-cancer agent. Its biological activities are being studied to understand its mechanisms of action and to develop new therapeutic strategies for the treatment of various types of cancer.
Used in Drug Delivery Systems:
To enhance the delivery and efficacy of (6-(methylthio)pyridin-3-yl)methanol, novel drug delivery systems are being developed. These systems aim to improve the bioavailability and therapeutic outcomes of the compound by employing various carriers, such as organic and metallic nanoparticles, for targeted and controlled release.
Check Digit Verification of cas no
The CAS Registry Mumber 101990-65-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,9,9 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 101990-65:
(8*1)+(7*0)+(6*1)+(5*9)+(4*9)+(3*0)+(2*6)+(1*5)=112
112 % 10 = 2
So 101990-65-2 is a valid CAS Registry Number.
101990-65-2Relevant articles and documents
MUSCARINIC M1 RECEPTOR POSITIVE ALLOSTERIC MODULATORS
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, (2018/03/25)
The present invention relates to compounds of formula (I), or their isotopic forms, stereoisomers, tautomers or pharmaceutically acceptable salt (s) thereof as muscarinic M1 receptor positive allosteric modulators (M1 PAMs). The present invention describes the preparation, pharmaceutical composition and the use of compound formula (I).
HETEROCYCLIC FUSED PHENANTHROLINONE M1 RECEPTOR POSITIVE ALLOSTERIC MODULATORS
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, (2012/01/06)
The present invention is directed to heterocyclic fused phenanthrolinone compounds of formula (I) which are M1 receptor positive allosteric modulators and that are useful in the treatment of diseases in which the M1 receptor is involved, such as Alzheimer's disease, schizophrenia, pain or sleep disorders. The invention is also directed to pharmaceutical compositions comprising the compounds, and to the use of the compounds and compositions in the treatment of diseases mediated by the M1 receptor.
1-pyridylmethyl-2-nitromethylene-1,3-diazacycloalkane insecticides
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, (2008/06/13)
Novel insecticides of the formula STR1 in which R is a hydrogen atom or a lower alkyl group, X is a halogen atom, a lower alkyl group, a lower alkoxy group, a lower alkylthio-group, a lower alkylsulfinyl group, a lower alkylsulfonyl group, a lower alkenyl group, a lower alkynyl group, an aryl group, an aryloxy group which may be optionally substituted by a halogen atom, an arylthio group which may be optionally substituted by a halogen atom, or an aralkyl group, l is 1, 2, 3 or 4, m is 2, 3, or 4, and n is 0, 1, 2 or 3, or salts thereof. Intermediates therefor of the formula STR2 are also new.
