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Cyclohexanone, 2-[(R)-(4-bromophenyl)hydroxymethyl]-, (2R)-rel- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119752-02-2

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119752-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119752-02-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,7,5 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 119752-02:
(8*1)+(7*1)+(6*9)+(5*7)+(4*5)+(3*2)+(2*0)+(1*2)=132
132 % 10 = 2
So 119752-02-2 is a valid CAS Registry Number.

119752-02-2Relevant academic research and scientific papers

Direct aldol reactions catalyzed by a heterogeneous guanidinium salt/proline system under solvent-free conditions

Martinez-Castaneda, Angel,Poladura, Belen,Rodriguez-Solla, Humberto,Concellon, Carmen,Del Amo, Vicente

, p. 3032 - 3035 (2011)

The combined activity of (S)-proline and an achiral cocatalyst (a TBD-derived guanidinium salt) allow direct aldol reactions to be carried out with high diastereoselectivity and enantioselectivity under solvent-free conditions with a rather simple reactio

Gelatin protein-mediated direct Aldol reaction

Kühbeck, Dennis,Bachl, Jürgen,Sch?n, Eva-Maria,Gotor-Fernández, Vicente,Díaz Díaz, David

, p. 574 - 580 (2014)

Gelatin protein was found to catalyze the aldol reaction between cyclohexanone and different aromatic aldehydes under mild reaction conditions. The aldol additions carried out in DMSO at 37 yielded the addition products with moderate diastereoselectivitie

Asymmetric organocatalytic direct aldol reactions of cyclohexanone with aldehydes in brine

Huang, Wen-Ping,Chen, Jia-Rong,Li, Xin-Yong,Cao, Yi-Ju,Xiao, Wen-Jing

, p. 208 - 213 (2007)

Organocatalytic asymmetric direct aldol reactions in brine with high diastereo- and enantioselectivities, using a readily available bifunctional amide catalyst, were developed.

Highly diastereoselective preparation of aldol products using new functionalized allylic aluminum reagents

Shen, Zhi-Liang,Peng, Zhihua,Yang, Chun-Ming,Helberg, Julian,Mayer, Peter,Marek, Ilan,Knochel, Paul

, p. 956 - 959 (2014)

Chloro-substituted triethylsilyl enol ethers derived from cyclohexanone and related ketones are converted with aluminum powder in the presence of indium trichloride to functionalized allylic aluminum reagents which represent a new type of synthetic equiva

Rationally designed organocatalyst for direct asymmetric aldol reaction in the presence of water

Wang, Chao,Jiang, Yi,Zhang, Xiao-xia,Huang, Yi,Li, Bo-gang,Zhang, Guo-lin

, p. 4281 - 4285 (2007)

A rationally designed organocatalyst for direct asymmetric aldol reaction in the presence of water has been developed. High yield (up to 99%), diastereoselectivity (up to 99:1) and enantioselectivity (up to 97%) were obtained under optimal conditions.

Highly efficient threonine-derived organocatalysts for direct asymmetrie aldol reactions in water

Wu, Xiaoyu,Jiang, Zhaoqin,Shen, Han-Ming,Lu, Yixin

, p. 812 - 816 (2007)

The introduction of siloxy groups at the hydroxy function of natural threonine resulted in efficient hydrophobic organocatalysts, which could efficiently catalyze the direct aldol reactions of both cyclic and acyclic ketones with aromatic aldehydes in wat

Self-assembled Polydiacetylene Nanoribbons for Semi-heterogeneous and Enantioselective Organocatalysis of Aldol Reactions in Water

Hoang, Minh-Duc,Kumar, Ramar Arun,Buisson, David A.,Ling, Wai Li,Gravel, Edmond,Doris, Eric

, p. 1156 - 1160 (2020)

We report the synthesis, characterization, and supra-molecular assembly of novel diacetylene amphiphilic units bearing a chiral proline-derived head group. In water, these amphiphiles self-assemble into twisted ribbons that are photo-polymerized to afford

Enantioselective aldol reaction of trimethoxysilyl enol ethers with aldehydes catalyzed by p-Tol-BINAP·AgF complex

Yanagisawa,Nakatsuka,Asakawa,Kageyama,Yamamoto

, p. 69 - 72 (2001)

New catalytic asymmetric Mukaiyama-type aldol reaction using trimethoxysilyl enol ethers was achieved using p-Tol-BINAP·AgF complex as a catalyst. High syn- and enantioselectivities were obtained both from the E- and Z-silyl enol ethers.

Polydopamine - An organocatalyst rather than an innocent polymer

Mrowczynski, Radoslaw,Bunge, Alexander,Liebscher, Juergen

, p. 8647 - 8653 (2014)

Polydopamine (PDA) is easily available by oxidation of dopamine and is widely used for persistent coatings of various materials. It is hitherto considered to be inert in many interesting biomedical and other applications. Results presented here, reveal an unexpected behavior of polydopamine as an organocatalyst in direct aldol reactions under mild conditions. Evidence was found for dual catalysis making use of amino and phenolic hydroxy groups found in PDA. Thus scientists must be aware that PDA is not an innocent polymer and can cause unwanted side effects in important applications, such as in biomedicine or as supports in catalysis.

An efficient ionic liquid additive for proline-catalyzed direct asymmetric aldol reactions between cyclic ketones and aromatic aldehydes

Qian, Yunbo,Zheng, Xin,Wang, Xu,Xiao, Shiyong,Wang, Yongmei

, p. 576 - 577 (2009)

An ionic liquid [EMIm][CF3COO] proved to be an efficient additive for proline-catalyzed direct asymmetric aldol reactions between cyclic ketones and aromatic aldehydes in [BMIm]BF4 at room temperature. Corresponding aldol products in

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