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(1R)-5,5',6,6',7,7',8,8'-octahydro-3,3'-bis[2,4,6-tris(1-Methylethyl)phenyl]-[1,1'-Binaphthalene]-2,2'-diol is a complex organic compound belonging to the binaphthalene class. It features a molecular formula of C90H102O2 and a molecular weight of 1256.73 g/mol. As a chiral molecule, it exists in the (1R) configuration and possesses a non-superimposable mirror image. Its structure is characterized by multiple phenyl groups attached to the binaphthalene core.

1522367-79-8

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1522367-79-8 Usage

Uses

Used in Asymmetric Catalysis:
(1R)-5,5',6,6',7,7',8,8'-octahydro-3,3'-bis[2,4,6-tris(1-Methylethyl)phenyl]-[1,1'-Binaphthalene]-2,2'-diol is utilized as a chiral ligand in asymmetric catalysis, enabling the selective synthesis of enantiomerically pure compounds. This is crucial for the production of pharmaceuticals and other chiral molecules, where the stereochemistry can significantly impact biological activity.
Used in Chromatography:
In chromatography, (1R)-5,5',6,6',7,7',8,8'-octahydro-3,3'-bis[2,4,6-tris(1-Methylethyl)phenyl]-[1,1'-Binaphthalene]-2,2'-diol serves as a chiral resolving agent. It aids in the separation of enantiomers, which is essential for determining the purity and composition of chiral compounds in various industries, including pharmaceuticals and agrochemicals.
Used in Organic Synthesis:
(1R)-5,5',6,6',7,7',8,8'-octahydro-3,3'-bis[2,4,6-tris(1-Methylethyl)phenyl]-[1,1'-Binaphthalene]-2,2'-diol is also employed in organic synthesis for the preparation of various chiral compounds. Its unique structure and chiral properties make it a valuable building block for the development of new molecules with potential applications in various fields.
Used in Pharmaceutical Production:
(1R)-5,5',6,6',7,7',8,8'-octahydro-3,3'-bis[2,4,6-tris(1-Methylethyl)phenyl]-[1,1'-Binaphthalene]-2,2'-diol (1R)-5,5',6,6',7,7',8,8'-octahydro-3,3'-bis[2,4,6-tris(1-Methylethyl)phenyl]-[1,1'-Binaphthalene]-2,2'-diol plays a significant role in the production of pharmaceuticals. Its applications in asymmetric catalysis and chromatography contribute to the synthesis and purification of enantiomerically pure drugs, which is vital for ensuring the safety and efficacy of medications.

Check Digit Verification of cas no

The CAS Registry Mumber 1522367-79-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,2,2,3,6 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1522367-79:
(9*1)+(8*5)+(7*2)+(6*2)+(5*3)+(4*6)+(3*7)+(2*7)+(1*9)=158
158 % 10 = 8
So 1522367-79-8 is a valid CAS Registry Number.

1522367-79-8Upstream product

1522367-79-8Downstream Products

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