60536-98-3 Usage
Description
2,2'-Dimethyl-1,1'-binaphthalene (CAS# 60536-98-3) is an organic compound that serves as a valuable building block in the synthesis of various organic molecules. Its unique structure, featuring two methyl groups attached to a binaphthalene core, makes it a versatile intermediate for creating complex organic compounds.
Uses
Used in Organic Synthesis:
2,2'-Dimethyl-1,1'-binaphthalene is used as a key intermediate in the synthesis of complex organic molecules for various applications. Its presence in the molecule allows for the formation of new chemical bonds and the creation of diverse structures, which can be further modified to achieve desired properties.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,2'-Dimethyl-1,1'-binaphthalene is used as a starting material for the development of new drugs. Its unique structure can be modified to create potential drug candidates with specific therapeutic properties, contributing to the discovery of novel treatments for various diseases.
Used in Chemical Research:
2,2'-Dimethyl-1,1'-binaphthalene is also utilized in chemical research to study the properties and reactivity of organic compounds. Its structure provides a platform for investigating various chemical reactions and mechanisms, furthering our understanding of organic chemistry and its applications.
Used in Material Science:
In the field of material science, 2,2'-Dimethyl-1,1'-binaphthalene can be employed as a component in the development of new materials with specific properties. Its incorporation into polymers or other materials can lead to the creation of materials with tailored characteristics, such as improved stability, solubility, or conductivity.
Check Digit Verification of cas no
The CAS Registry Mumber 60536-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,5,3 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 60536-98:
(7*6)+(6*0)+(5*5)+(4*3)+(3*6)+(2*9)+(1*8)=123
123 % 10 = 3
So 60536-98-3 is a valid CAS Registry Number.
60536-98-3Relevant articles and documents
Application of a Ferrocene-Based Palladacycle Precatalyst to Enantioselective Aryl-Aryl Kumada Coupling
Arthurs, Ross A.,Hughes, David L.,Richards, Christopher J.
supporting information, (2022/02/21)
The palladium catalysed reaction of 1-iodo-2-methylnaphthalene and 2-methyl-1-naphthylmagnesium bromide gave quantitatively an (Sa)-configured cross-coupled product in 80 % e.e. using (R,Sp)-PPFA as a ligand. N,N-Dimethylaminomethylferrocene was cyclopalladated (Na2PdCl4, (S)?Ac?Phe?OH, 93 % e.e., as determined by 1H NMR as a result of self-induced non-equivalence), and the resulting (Sp)-configured dimeric palladacycle was employed as a precatalyst for this cross-coupling reaction (5 mol%). Addition to the palladacycle of diphenylphosphine and subsequent base-promoted bidentate ligand synthesis and palladium capture gave an in situ generated catalyst resulting in an (Sp)-configured product in up to 71 % e.e.
NOVEL CHIRAL DIHYDROBENZOAZAPHOSPHOLE LIGANDS AND SYNTHESIS THEREOF
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Paragraph 0145; 0146, (2018/06/15)
This invention relates to novel phosphorous ligands useful for organic transformations. Methods of making and using the ligands in organic synthesis are described. The invention also relates to processes for preparing the novel ligands.
A Binaphthyl-Based Scaffold for a Chiral Dirhodium(II) Biscarboxylate Ligand with α-Quaternary Carbon Centers
Chen, Po-An,Setthakarn, Krit,May, Jeremy A.
, p. 6155 - 6161 (2017/09/15)
A chiral dirhodium(II) paddlewheel complex has been synthesized from biscarboxylate ligands derived from BINOL, and the resulting complex has been used in enantioselective carbene/alkyne cascade reactions. The ligand design was guided by requirements of α
