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N,N'-(1R,2R)-(-)-1,2-cyclohexylenebis(2-hydroxy-3-methoxy-benzyldeneimine) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

181787-60-0

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181787-60-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 181787-60-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,7,8 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 181787-60:
(8*1)+(7*8)+(6*1)+(5*7)+(4*8)+(3*7)+(2*6)+(1*0)=170
170 % 10 = 0
So 181787-60-0 is a valid CAS Registry Number.

181787-60-0Downstream Products

181787-60-0Relevant academic research and scientific papers

Asymmetric Oxidation of Sulfides to Sulfoxides by Organic Hydroperoxides with Optically Active Schiff Base-Oxovanadium(IV) Catalysts

Nakajima, Kiyohiko,Kojima, Masaaki,Fujita, Junnosuke

, p. 1483 - 1486 (1986)

The asymmetric oxidation of sulfides into the corresponding sulfoxides was achieved with organic hydroperoxides in the presence of a catalytic amount of optically active Schiff base-oxovanadium(IV) complexes; in most cases the optical yields (e.e.) ranged

A pair of chiral Cu(II)-Tb(III)-Fe(III) heterotrimetallic enantiomers: Structural, luminescent, and magnetic studies

Wang, Zi-Xuan,Yuan, Ya-Nan,Wang, Qing-Lun,Wang, Qi,Meng, Xiang-Jian,Yang, Chun

, p. 2177 - 2184 (2021/09/20)

One chiral heterotrimetallic compound, [Cu(H2O){(R,R)-valcy}Tb(CH3OH)2(H2O)(μ-CN)Fe(CN)5]·[Cu(H2O){(R,R)-valcy}Tb(CH3OH)1.5(H2O)1.5(μ-CN)Fe(CN)s

Synthesis, Characterization, and in Vitro Cytotoxicity of Platinum(II) Complexes Bearing Chiral Tetradentate Salicylaldimine Ligands

Nguyen, Quang Trung,Nguyen, Van Tuyen,Pham Thi, Phuong Nam

, (2020/07/21)

A series of platinum(II) complexes with chiral Schiff base ligands derived from various salicylaldehydes with (R,R′)- and (S,S′)-cyclohexanediamine were synthesized and characterized by ESI-MS, IR, and NMR. Obtained spectra with typical signals were in agreement with suggested molecular formulae of the complexes. Their photophysical properties were studied by UV-visible and emission spectroscopies. The UV-Vis showed the typical band with low energy at visible range 400-500 nm for MLCT, and this band can emit the luminescent band with emission maximum wavelengths at 529-595 nm. The in vitro cytotoxicity of obtained platinum(II) complexes was screened for KB and MCF-7 human cancer cell lines. The results showed that (S)-enantiomers were more active than (R)-enantiomers and the different positions of methoxy group in salicyl ring gave different cytotoxicities.

Temperature-controlled polymorphism of chiral CuII-LnIII dinuclear complexes exhibiting slow magnetic relaxation

Wen, He-Rui,Bao, Jun,Liu, Sui-Jun,Liu, Cai-Ming,Zhang, Cai-Wei,Tang, Yun-Zhi

, p. 11191 - 11201 (2015/06/25)

A new family of 3d-4f dinuclear complexes derived from a chiral Schiff-base ligand, (R,R)-N,N′-bis(3-methoxysalicylidene)cyclohexane-1,2-diamine (H2L), has been synthesized and structurally characterized, namely, [Cu(L)Ln(NO3)3

A family of nickel-lanthanide heterometallic dinuclear complexes derived from a chiral Schiff-base ligand exhibiting single-molecule magnet behaviors

Wen, He-Rui,Liu, Sui-Jun,Xie, Xin-Rong,Bao, Jun,Liu, Cai-Ming,Chen, Jing-Lin

, p. 274 - 282 (2015/08/06)

Abstract A new family of nickel-lanthanide heterometallic dinuclear complexes derived from a chiral Schiff-base ligand, (R,R)-N,N'-bis(3-methoxysalicylidene)cyclohexane-1,2-diamine (H2L), namely [Ni(L)Ln(NO3)3(H2/sub

A novel type of catalysts for the asymmetric C-C bond formation based on chiral stereochemically inert cationic Co iii complexes

Belokon,Larionov,Mkrtchyan,Khrustalev,Nijland,Saghyan,Godovikov,Peregudov,Babievsky,Ikonnikov,Maleev

, p. 2252 - 2260 (2013/10/01)

Schiff bases derived from (1R,2R)-1,2-diaminocyclohexane and 1 eq. of salycylic (or substituted salycylic) aldehyde form stereochemically inert positively charged chiral octahedral Co iii complexes of Δ-configuration with the stereoselectivity approaching 100%. To evaluate the calatylic activity and stereoinduction of the resulting complexes with various counteranions in the outer sphere, a model reaction of trimethylsilyl cyanide addition to benzaldehyde was used. O-trimethylsilylmandelonitrile formed in the process had an enantiomeric purity up to 27%. Complexes with F - counterion showed high catalytic activity.

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