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2-[(E)-Benzylidene]cyclohexanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1467-15-8

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1467-15-8 Usage

Organic compound

Yes

Common uses

Pharmaceutical and fragrance industry

Physical state

Yellow liquid

Odor

Strong

Solubility

Insoluble in water, soluble in organic solvents

Raw material

Used in the synthesis of various pharmaceuticals and fragrances

Biological and pharmacological activities

Potential activities

Organic reactions

Used as a reactant, reagent, catalyst, and solvent

Versatility

Various applications in the chemical and pharmaceutical industries

Check Digit Verification of cas no

The CAS Registry Mumber 1467-15-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,6 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1467-15:
(6*1)+(5*4)+(4*6)+(3*7)+(2*1)+(1*5)=78
78 % 10 = 8
So 1467-15-8 is a valid CAS Registry Number.

1467-15-8Relevant academic research and scientific papers

Synthesis of hexahydrophenanthridines via the tandem reaction of benzynes

Li, Wen-Juan,Pian, Ji-Xin,Gu, Cheng-Zhi,Dai, Bin,He, Lin

, (2020)

A tandem insertion-cyclization reaction between carbocyclic β–amino ketones and benzynes has been described, producing hexahydrophenanthridines in moderate to high yields.

The reaction of enaminones with grignard reagents: Synthesis of α,β- unsaturated ketones

Fontenas,Ait-Haddou,Bejan,Balavoine

, p. 1743 - 1753 (1998)

Enaminones in toluene react with Grignard reagents in tetrahydrofuran at 0-25 °C, to give selectively and with high yields the corresponding α,β- unsaturated ketones.

Novel chalcones derivatives with potential antineoplastic activity investigated by docking and molecular dynamics simulations

Neto, Raimundo de A. M.,Santos, Cleydson B. R.,Henriques, Shayanne V. C.,Machado, Letícia de O.,Cruz, Jorddy N.,da Silva, Carlos H. T. de P.,Federico, Leonardo B.,Oliveira, Edivaldo H. C. de,de Souza, Michel P. C.,da Silva, Patrícia N. B.,Taft, Carlton A.,Ferreira, Irlon M.,Gomes, Madson R. F.

, (2020)

Glioblastoma is an aggressive primary tumor of the central nervous system (CNS). Is the most aggressive among infiltrative gliomas arising from the CNS. This tumor has low patient survival rate and several studies aiming at developing new drugs have increased. Patients with this cancer type face significant morbidity and mortality. This study evaluated the antineoplastic activity of synthetic chalcones (3a-3f) using in vitro glioblastoma models and molecular modeling. Cytotoxicity assay showed that Astrocitoma Hospital Ofir Loyola No 1 (AHOL1) and Uppsala 87 neoplastic glioblastoma lines (U87) cellular viability were significantly reduced compared to Healthy human fibroblasts cell lines (AN27) when exposed to chalcones. Interaction with the serine amino acid was present in the most promising and the reference binder docking, suggesting its importance inhibiting cell growth. Comparative analysis between the reference ligands and the molecules showed that the amino acid LYS352 present in all fittings, suggesting that this is the main amino acid for interaction with tubulin and are consistent with those in cytotoxicity assay, suggesting antineoplastic potential in glioblastoma. Long trajectory molecular dynamics studies were also carried out in order to investigate stability and conformations amongst the chalcones bound tubulin as well, in comparison to doxorubicin (here used as control), however future studies are needed to further assess the mechanism of inhibition of chalcones used in this investigation. Communicated by Ramaswamy H. Sarma.

Remarkably chemoselective reduction of unmodified Baylis-Hillman adducts by InCl3/NaBH4: Application to the stereoselective synthesis of trisubstituted alkenones including two alarm pheromones

Das, Biswanath,Banerjee, Joydeep,Chowdhury, Nikhil,Majhi, Anjoy,Holla, Harish

, p. 1879 - 1882 (2006)

A novel, convenient and solely stereoselective synthesis of trisubstituted E-alkenones has been achieved by InCl3/NaBH4 mediated chemoselective reduction of unmodified Baylis-Hillman adducts derived from vinyl ketones and cycloalkenones for the first time. The efficiency of this methodology in the practical synthesis of (S)-(+)-manicone and (S)-(+)-normanicone, two alarm pheromones of Manica ants, has been demonstrated. Georg Thieme Verlag Stuttgart.

Activated charcoal-mediated synthesis of chalcones catalyzed by NaOH in water

Tanemura, Kiyoshi,Rohand, Taoufik

, (2021/02/27)

A variety of chalcones were synthesized in good yields by the activated charcoal-mediated aldol reactions between benzaldehydes and acetophenones catalyzed by NaOH in water. 2,6-Bis((E)-benzylidene)cyclohexan-1-ones were prepared by the aldol reactions between benzaldehydes and cyclohexanone. Activated charcoal could be recycled five times without the significant decrease of yields.

Highly Enantioselective Iridium-Catalyzed Hydrogenation of Conjugated Trisubstituted Enones

Peters, Bram B. C.,Jongcharoenkamol, Jira,Krajangsri, Suppachai,Andersson, Pher G.

supporting information, p. 242 - 246 (2021/01/13)

Asymmetric hydrogenation of conjugated enones is one of the most efficient and straightforward methods to prepare optically active ketones. In this study, chiral bidentate Ir-N,P complexes were utilized to access these scaffolds for ketones bearing the stereogenic center at both the α- and β-positions. Excellent enantiomeric excesses, of up to 99%, were obtained, accompanied with good to high isolated yields. Challenging dialkyl substituted substrates, which are difficult to hydrogenate with satisfactory chiral induction, were hydrogenated in a highly enantioselective fashion.

Redox-Neutral Cobalt(III)-Catalyzed C-H Activation/Annulation of α,β-Unsaturated Oxime Ether with Alkyne: One-Step Access to Multisubstituted Pyridine

Mohanty, Smruti Ranjan,Pati, Bedadyuti Vedvyas,Banjare, Shyam Kumar,Das Adhikari, Gopal Krushna,Ravikumar, Ponneri Chandrababu

, p. 1074 - 1083 (2021/01/14)

A redox neutral Co(III)-catalyzed annulation of α,β-unsaturated oxime ether with alkyne has been reported. Multisubstituted pyridines were synthesized in good yields without the use of any heavy metal oxidants. The developed methodology tolerates a variety of functional groups. Notably, this transformation has been applied to the late-stage modification of the bioactive molecule dehydropregnenolone.

Ruthenium-catalysed synthesis of chiral exocyclic allylic alcoholsviachemoselective transfer hydrogenation of 2-arylidene cycloalkanones

Zhang, Kaili,Liu, Qixing,He, Renke,Chen, Danyi,Deng, Zhangshuang,Huang, Nianyu,Zhou, Haifeng

supporting information, p. 1628 - 1632 (2021/03/09)

An exclusive asymmetric reduction of C=O bonds of 2-arylidene four-, five-, six-, and seven-membered cycloalkanones has been studied systematically. The asymmetric transfer hydrogenation was performed using a robust and commercially available chiral diamine-derived ruthenium complex as a catalyst and HCOOH/Et3N as a hydrogen source under mild conditions, giving 51 examples of chiral exocyclic allylic alcohols in up to 96% yield and 99% ee. This method was also applicable to the gram-scale synthesis of the active intermediates of the anti-inflammatory loxoprofen and natural product (?)-goniomitine.

Rhodium-catalyzed asymmetric hydrogenation of exocyclic α,β-unsaturated carbonyl compounds

Yang, Jiaxin,Li, Xiuxiu,You, Cai,Li, Shuailong,Guan, Yu-Qing,Lv, Hui,Zhang, Xumu

supporting information, p. 856 - 859 (2020/02/15)

A highly enantioselective hydrogenation of exocyclic α,β-unsaturated carbonyl compounds catalyzed by Rh/bisphosphine-thiourea (ZhaoPhos) has been developed, giving the corresponding α-chiral cyclic lactones, lactams and ketones with high yields and excellent enantioselectivities (up to 99% yield and 99% ee). Remarkably, the hydrogen bond between the substrate and the catalyst plays a critical role in this transformation. The synthetic utility of this protocol has been demonstrated by efficient synthesis of chiral 3-(4-fluorobenzyl)piperidine, a key chiral fragment of bioactive molecules.

Novel racemic chiral organic boron nitrogen fluorescent compound and preparation method thereof (by machine translation)

-

Paragraph 0118-0125, (2020/05/05)

The novel chiral organic boron nitride fluorescent compound, is characterized in that, takes a cheap,readily available monoiodobenzene derivative, carboxylic acid derivative as a raw material, to react at a certain temperature with a common organic solvent as a reaction solvent, for a certain time, high yield, to selectively obtain a novel chiral organic boron nitrogen fluorescent compound . The catalyst, can be recovered, at a certain temperature for a certain period of time for a certain period of time to produce a novel chiral organic boron-nitrogen fluorescent compound with low cost,and a high yield, and selectivity, can be, obtained at a certain temperature for a certain period, of time with a certain period of time and high yield. (by machine translation)

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