223389-51-3 Usage
Description
R-2,2'-bis(methoxymethoxy)-[1,1'-Binaphthalene]-3,3'-dicarboxaldehyde is a chiral chemical compound belonging to the binaphthalene family, characterized by its molecular formula C30H24O6. It is renowned for its high efficiency in asymmetric synthesis and serves as a crucial chiral ligand in numerous catalytic reactions.
Uses
Used in Pharmaceutical Industry:
R-2,2'-bis(methoxymethoxy)-[1,1'-Binaphthalene]-3,3'-dicarboxaldehyde is utilized as a chiral building block for the synthesis of chiral pharmaceuticals. Its unique properties enable the creation of complex molecular structures with high selectivity, which is essential for developing new drugs with improved efficacy and reduced side effects.
Used in Agrochemical Industry:
In the agrochemical sector, R-2,2'-bis(methoxymethoxy)-[1,1'-Binaphthalene]-3,3'-dicarboxaldehyde is employed as a key intermediate in the production of chiral agrochemicals and fine chemicals. Its ability to enhance the selectivity and efficiency of chemical reactions contributes to the development of more effective and environmentally friendly agrochemical products.
Used in Organic Synthesis:
R-2,2'-bis(methoxymethoxy)-[1,1'-Binaphthalene]-3,3'-dicarboxaldehyde is used as a chiral ligand in various catalytic reactions, facilitating the synthesis of enantiomerically pure compounds. This is particularly important in organic synthesis, where the ability to produce specific enantiomers can significantly impact the biological activity and safety of the resulting compounds.
Used in Research and Development:
Due to its high efficiency in asymmetric synthesis, R-2,2'-bis(methoxymethoxy)-[1,1'-Binaphthalene]-3,3'-dicarboxaldehyde is a valuable tool for researchers and chemists in the development of new drugs and chemicals. Its unique properties allow for the exploration of novel synthetic pathways and the creation of innovative molecular structures with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 223389-51-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,3,8 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 223389-51:
(8*2)+(7*2)+(6*3)+(5*3)+(4*8)+(3*9)+(2*5)+(1*1)=133
133 % 10 = 3
So 223389-51-3 is a valid CAS Registry Number.
223389-51-3Relevant articles and documents
ESIPT-based ratiometric probe for Zn2+ detection based on BINOL framework
Zhang, Kewei,Wu, Shengying,Qu, Dahui,Wang, Limin
, p. 1133 - 1137 (2016)
A ratiometric BINOL-based fluorescent probe for Zn2+ detection was rationally designed and synthesized. Based on the excited-state intramolecular proton transfer (ESIPT) mechanisms, the probe exhibited a significant variation on emission wavele
Compound boranil based on bi bisnaphthol of the framework and its preparation and use
-
, (2016/10/24)
The invention provides a series of Boranil compounds based on 1,1'-binaphthol parents, a preparation method of the compounds, and application of the compounds on detection of fluorine ions. The compounds meet one of the following general formulas, X is on
Chiral Ti(IV) complexes of hexadentate Schiff bases as precatalysts for aldehyde allylation: unusual additive effect of trimethylsilyl chloride
Belokon, Yuri N.,Chusov, Denis,Borkin, Dmitry A.,Yashkina, Lidia V.,Bolotov, Pavel,Skrupskaya, Tatiana,North, Michael
, p. 459 - 466 (2008/09/19)
Chiral dinuclear titanium(IV) complexes have been found to be more effective catalysts for the asymmetric allylation of p-nitrobenzaldehyde than their mononuclear analogues. The addition of trimethylsilyl chloride to the reaction mixture decreases the rate of the background reaction and increases the yield of the reaction catalysed by the dinuclear complex.
