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(4S,4'S)-2,2'-(1,3-bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(4-benzyl-4,5-dihydrooxazole) is a complex organic molecule with a molecular formula of C63H71N3O4. It is a chiral compound, characterized by its 4S,4'S configuration, and is known for its unique structure that includes multiple benzyl and tert-butyl groups, as well as a bis(4,5-dihydrooxazole) moiety. (4S,4'S)-2,2'-(1,3-bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(4-benzyl-4,5-dihydrooxazole) is often utilized as a ligand in coordination chemistry and serves as a building block in the synthesis of other organic compounds. Its distinctive structural features and functional groups render it valuable for a range of chemical and pharmaceutical applications.

2172801-78-2

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2172801-78-2 Usage

Uses

Used in Coordination Chemistry:
(4S,4'S)-2,2'-(1,3-bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(4-benzyl-4,5-dihydrooxazole) is used as a ligand in coordination chemistry for its ability to form stable complexes with metal ions. (4S,4'S)-2,2'-(1,3-bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(4-benzyl-4,5-dihydrooxazole)'s chiral nature and diverse functional groups allow for the creation of complexes with unique properties and potential applications in various fields.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, (4S,4'S)-2,2'-(1,3-bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(4-benzyl-4,5-dihydrooxazole) is used as a building block for the synthesis of new drugs. Its structural complexity and functional group diversity make it a valuable component in the development of innovative pharmaceutical compounds with potential therapeutic effects.
Used in Organic Synthesis:
(4S,4'S)-2,2'-(1,3-bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(4-benzyl-4,5-dihydrooxazole) is also utilized as a key component in organic synthesis, where it can be used to construct a variety of complex organic molecules. Its unique structure and functional groups facilitate the creation of novel compounds with potential applications in various industries, including materials science, agrochemicals, and specialty chemicals.
Used in Research and Development:
(4S,4'S)-2,2'-(1,3-bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(4-benzyl-4,5-dihydrooxazole) is employed in research and development settings to study its properties and potential applications. The chiral nature and complex structure of (4S,4'S)-2,2'-(1,3-bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(4-benzyl-4,5-dihydrooxazole) make it an interesting subject for scientific investigation, which could lead to new discoveries and advancements in related fields.

Check Digit Verification of cas no

The CAS Registry Mumber 2172801-78-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,1,7,2,8,0 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2172801-78:
(9*2)+(8*1)+(7*7)+(6*2)+(5*8)+(4*0)+(3*1)+(2*7)+(1*8)=152
152 % 10 = 2
So 2172801-78-2 is a valid CAS Registry Number.

2172801-78-2Downstream Products

2172801-78-2Relevant academic research and scientific papers

Cobalt-Catalyzed Enantioselective Negishi Cross-Coupling of Racemic α-Bromo Esters with Arylzincs

Liu, Feipeng,Zhong, Jiangchun,Zhou, Yun,Gao, Zidong,Walsh, Patrick J.,Wang, Xueyang,Ma, Sijie,Hou, Shicong,Liu, Shangzhong,Wang, Minan,Wang, Min,Bian, Qinghua

, p. 2059 - 2064 (2018)

The first cobalt-catalyzed enantioselective Negishi cross-coupling reaction, and the first arylation of α-halo esters with arylzinc halides, are disclosed. Employing a cobalt-bisoxazoline catalyst, various α-arylalkanoic esters were synthesized in excellent enantioselectivities and yields (up to 97 % ee and 98 % yield). A diverse range of functional groups, including ether, halide, thioether, silyl, amine, ester, acetal, amide, olefin and heteroaromatics is tolerated by this method. This method was suitable for gram-scale reactions, enabling the synthesis of (R)-xanthorrhizol with high enantiopurity. Radical clock experiments support the intermediacy of radicals.

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