17337-96-1 Usage
Uses
Used in Pharmaceutical Industry:
[2,2'-Binaphthalene]-8,8'-dicarboxaldehyde,1,1',6,6',7,7'-hexahydroxy-3,3'-dimethyl-5,5'-bis(1-methylethyl)-, 8,8'-dioxime is used as a chiral building block for the synthesis of various pharmaceutical compounds. Its unique binaphthalene core and multiple functional groups allow for the creation of novel drugs with improved efficacy and selectivity.
Used in Chemical Synthesis:
In the field of chemical synthesis, [2,2'-Binaphthalene]-8,8'-dicarboxaldehyde,1,1',6,6',7,7'-hexahydroxy-3,3'-dimethyl-5,5'-bis(1-methylethyl)-, 8,8'-dioxime serves as a versatile intermediate for the production of a variety of complex molecules. Its multiple reactive sites facilitate the formation of new chemical bonds and the synthesis of target compounds.
Used in Material Science:
[2,2'-Binaphthalene]-8,8'-dicarboxaldehyde,1,1',6,6',7,7'-hexahydroxy-3,3'-dimethyl-5,5'-bis(1-methylethyl)-, 8,8'-dioxime is used as a key component in the development of advanced materials, such as chiral polymers and optically active materials. Its unique structure and functional groups contribute to the creation of materials with specific properties and applications.
Used in Chiral Catalysis:
In the field of asymmetric synthesis and chiral catalysis, [2,2'-Binaphthalene]-8,8'-dicarboxaldehyde,1,1',6,6',7,7'-hexahydroxy-3,3'-dimethyl-5,5'-bis(1-methylethyl)-, 8,8'-dioxime is used as a chiral ligand or catalyst to promote enantioselective reactions. Its binaphthalene core and multiple functional groups enhance the selectivity and efficiency of these processes, leading to the production of enantiomerically pure compounds.
Used in Analytical Chemistry:
[2,2'-Binaphthalene]-8,8'-dicarboxaldehyde,1,1',6,6',7,7'-hexahydroxy-3,3'-dimethyl-5,5'-bis(1-methylethyl)-, 8,8'-dioxime is employed as a chiral selector in various analytical techniques, such as chromatography and capillary electrophoresis. Its unique structure allows for the separation and analysis of enantiomers, providing valuable information on the stereochemistry of chiral compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 17337-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,3 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17337-96:
(7*1)+(6*7)+(5*3)+(4*3)+(3*7)+(2*9)+(1*6)=121
121 % 10 = 1
So 17337-96-1 is a valid CAS Registry Number.
