43109-77-9 Usage
Description
o-AdaMantylanisole is an Adamantane anisole derivative, which is a versatile compound with unique structural and chemical properties. It is characterized by the presence of an adamantane moiety, a highly stable and rigid carbon cage structure, and an anisole group, which provides additional functionalization and reactivity. This combination of features makes o-AdaMantylanisole a valuable building block in organic synthesis and a promising candidate for various applications in different industries.
Uses
Used in Organic Synthesis:
o-AdaMantylanisole is used as a synthetic intermediate for the preparation of various adamantane derivatives. Its unique structure and reactivity make it a valuable component in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Amino Acid and Peptide Synthesis:
o-AdaMantylanisole is used as a protective group in amino acid and peptide synthesis. The 1-adamantyl, 1-adamantylthio, and 1-adamantylsulfinyl groups derived from o-AdaMantylanisole provide a stable and easily removable protection for amino acid functional groups, facilitating the synthesis of complex peptide sequences and improving the overall efficiency of the process.
Used in Pharmaceutical Industry:
o-AdaMantylanisole and its derivatives have potential applications in the pharmaceutical industry, where they can be used as building blocks for the development of new drugs or as components of drug delivery systems. Their unique structure and properties may contribute to improved pharmacokinetics, enhanced target selectivity, and reduced side effects.
Used in Agrochemical Industry:
In the agrochemical industry, o-AdaMantylanisole and its derivatives can be employed as active ingredients in the development of new pesticides, herbicides, or other crop protection agents. Their unique chemical properties may provide novel modes of action, improved efficacy, and reduced environmental impact compared to existing products.
Used in Materials Science:
o-AdaMantylanisole and its derivatives can also find applications in materials science, where they can be used to develop new materials with unique properties. For example, they can be incorporated into polymers to improve their mechanical strength, thermal stability, or other physical properties, or used as components in the development of advanced materials for energy storage, electronics, or other high-tech applications.
Check Digit Verification of cas no
The CAS Registry Mumber 43109-77-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,1,0 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 43109-77:
(7*4)+(6*3)+(5*1)+(4*0)+(3*9)+(2*7)+(1*7)=99
99 % 10 = 9
So 43109-77-9 is a valid CAS Registry Number.
43109-77-9Relevant articles and documents
Flow Friedel–Crafts alkylation of 1-adamantanol with arenes using HO-SAS as an immobilized acid catalyst
Kasakado, Takayoshi,Hyodo, Mamoru,Furuta, Akihiro,Kamardine, Aina,Ryu, Ilhyong,Fukuyama, Takahide
, p. 2253 - 2257 (2020/12/15)
In this communication flow Friedel–Crafts alkylation was studied using hydroxy-substituted sulfonic acid-functionalized silica as a catalyst and 1-adamantanol as a model substrate. The reaction of 1-adamantanol (1a) with toluene (2a) proceeded well with 5 min of residence time at 120°C to give good yield of 1-tolyladamantane (3a) as a 1:9 mixture of meta and para isomers. When the flow synthesis was carried out over 2.5 hr of running time, the collected five fractions contain the product 3a in 97–92% yields, suggesting the durability of the catalyst.
Synthesis of functionalized adamantanes from fluoroadamantanes
Aoyama, Motoshi,Hara, Shoji
experimental part, p. 3682 - 3687 (2009/09/05)
Selective introduction of functional groups on the tert-carbon of adamantane was performed by substitution with fluorides. A methyl, phenacyl, aryl, cyclohexyl, alkoxy, or azido group was introduced into the adamantane skeleton without influencing the oth
