[1,1'-Binaphthalene]-2,2'-diol, 3,3'-bis(triphenylsilyl)is a complex chemical compound that belongs to the binaphthol derivatives family. It features two naphthalene rings connected by a central oxygen atom, with triphenylsilyl groups attached to the 3 and 3' positions of the naphthalene rings. [1,1'-Binaphthalene]-2,2'-diol, 3,3'-bis(triphenylsilyl)is known for its unique stereochemistry and ability to form stable complexes with various metal ions, making it a valuable asset in multiple scientific fields.
126911-86-2
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Basic information
- Product Name: [1,1'-Binaphthalene]-2,2'-diol, 3,3'-bis(triphenylsilyl)-
- Synonyms: [1,1'-Binaphthalene]-2,2'-diol, 3,3'-bis(triphenylsilyl)-
- CAS NO:126911-86-2
- Molecular Formula: C56H42O2Si2
- Molecular Weight: 803.10248
- EINECS: N/A
- Product Categories: N/A
- Mol File: 126911-86-2.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: /
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: [1,1'-Binaphthalene]-2,2'-diol, 3,3'-bis(triphenylsilyl)-(CAS DataBase Reference)
- NIST Chemistry Reference: [1,1'-Binaphthalene]-2,2'-diol, 3,3'-bis(triphenylsilyl)-(126911-86-2)
- EPA Substance Registry System: [1,1'-Binaphthalene]-2,2'-diol, 3,3'-bis(triphenylsilyl)-(126911-86-2)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 126911-86-2(Hazardous Substances Data)
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126911-86-2 Usage
Uses
Used in Asymmetric Synthesis:[1,1'-Binaphthalene]-2,2'-diol, 3,3'-bis(triphenylsilyl)is used as a chiral ligand for asymmetric synthesis, facilitating the creation of enantiomerically pure compounds. Its unique stereochemistry and complex formation capabilities with metal ions contribute to the high selectivity and efficiency of these reactions.
Used in Catalysis Reactions:
In the field of catalysis, [1,1'-Binaphthalene]-2,2'-diol, 3,3'-bis(triphenylsilyl)is employed as a chiral catalyst to enhance the selectivity and yield of various chemical reactions. Its ability to form stable complexes with metal ions plays a crucial role in the success of these catalytic processes.
Used in Organic Synthesis:
[1,1'-Binaphthalene]-2,2'-diol, 3,3'-bis(triphenylsilyl)is utilized in organic synthesis as a key building block for the development of novel organic compounds. Its unique structure and reactivity make it a valuable component in the synthesis of complex organic molecules.
Used in Materials Chemistry:
In materials chemistry, [1,1'-Binaphthalene]-2,2'-diol, 3,3'-bis(triphenylsilyl)is used to create advanced materials with specific properties. Its unique structure and ability to interact with other molecules contribute to the development of materials with tailored characteristics for various applications.
Used in Pharmaceutical Research:
[1,1'-Binaphthalene]-2,2'-diol, 3,3'-bis(triphenylsilyl)is also used in pharmaceutical research as a potential candidate for the development of new drugs. Its unique stereochemistry and complex formation capabilities make it a promising starting point for the design of novel therapeutic agents.
Used in Chemical Industry:
[1,1'-Binaphthalene]-2,2'-diol, 3,3'-bis(triphenylsilyl)is used as a chiral ligand and catalyst in the chemical industry for the production of enantiomerically pure compounds. Its high selectivity and efficiency in asymmetric synthesis make it a valuable tool for the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 126911-86-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,9,1 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.Calculate Digit Verification of CAS Registry Number 126911-86:
(8*1)+(7*2)+(6*6)+(5*9)+(4*1)+(3*1)+(2*8)+(1*6)=132
132 % 10 = 2
So 126911-86-2 is a valid CAS Registry Number.
126911-86-2Upstream product
126911-86-2Downstream Products
- 577700-85-7 (S)-[Ta(O2C20H10(SiPh3)2-3,3')(NHMe2)(NMe2)Cl2]
- 862593-77-9 ((C6H5)3SiC10H5O)2Ti(OC2H5)2
- 1263316-72-8 [((C10H5(Si(C6H5)3)O)2)Nb(N(CH3)2)3(HN(CH3)2)]
- 577700-90-4 (R,S)-[Ta(O2C20H10(SiPh3)2-3,3')(NHMe2)(NMe2)3]*(benzene)
- 371161-47-6 (C10H5OSi(C6H5)3)2AlCH2CH(CH3)2
- 883107-10-6 (R)-(C10H5(SiPh3))2O2Sc(o-C6H4CH2NMe2)(N,N-dimethylbenzylamine)
- 883107-11-7 (R)-(3,3'-bis(triphenylsilyl)-2,2'-oxido-1,1'-binaphthyl)(2-(dimethylaminomethyl)phenyl)(dimethylaminomethylphenyl)lutetium(III)
- 697807-13-9 (R)-(3,3'-bis(triphenylsilyl)-2,2'-oxido-1,1'-binaphthyl)(2-(dimethylaminomethyl)phenyl)(dimethylaminomethylphenyl)yttrium(III)
- 118724-91-7 (R)-{C10H5Si(C6H5)3}2O2AlCH3
- 548476-05-7 Al(CH2CH3)(py)((S)-3,3'-bis(triphenylsilyl)-1,1'-bi-2,2'-naphthoxide))
- 6125-66-2 AlMe3(pyridine)
- 548476-04-6 Al(CH3)(py)((S)-3,3'-bis(triphenylsilyl)-1,1'-bi-2,2'-naphthoxide))*C6H5CH3
- 577700-81-3 (R,S)-Ta(NMe2)3(C10H5(SiPh3)O)2NHMe2
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[1,1'-Binaphthalene]-2,2'-diol, 3,3'-bis(triphenylsilyl)-
