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2-Cyclopenten-1-one, 2-(hydroxyphenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

122617-89-4

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122617-89-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122617-89-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,6,1 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 122617-89:
(8*1)+(7*2)+(6*2)+(5*6)+(4*1)+(3*7)+(2*8)+(1*9)=114
114 % 10 = 4
So 122617-89-4 is a valid CAS Registry Number.

122617-89-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(hydroxy-phenyl-methyl)-cyclopent-2-en-1-one

1.2 Other means of identification

Product number -
Other names 2-(hydroxyphenylmethyl)-2-cyclopenten-1-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:122617-89-4 SDS

122617-89-4Relevant academic research and scientific papers

Asymmetric Morita-Baylis-Hillman reaction catalyzed by isophoronediamine- derived bis(thio)urea organocatalysts

Berkessel, Albrecht,Roland, Katrin,Neudoerfl, Joerg M.

, p. 4195 - 4198 (2006)

(Chemical Equation Presented) New and improved bis(thio)urea catalysts were synthesized from isophoronediamine (IPDA) and tested in the Morita-Baylis-Hillman reaction. The best results were achieved in the reaction of 2-cyclohexen-1-one with cyclohexaneca

The azoles: Effective catalysts for Baylis-Hillman reaction in basic water solution

Luo, Sanzhong,Mi, Xueling,Wang, Peng George,Cheng, Jin-Pei

, p. 5171 - 5174 (2004)

The azoles, which were inactive in neutral aqueous media, could be activated in alkaline solution and effectively catalyze the Baylis-Hillman reaction involving cyclic enones.

Enantioselective Morita-Baylis-Hillman (MBH) reaction promoted by a heterobimetallic complex with a Lewis base

Matsui, Katsuya,Takizawa, Shinobu,Sasai, Hiroaki

, p. 1943 - 1946 (2005)

A new double-activation catalysis is presented for the Morita-Baylis- Hillman (MBH) reaction of an α,β-unsaturated ketone and an aldehyde by the combined use of a heterobimetallic asymmetric complex and tributylphosphine ((n-Bu)3P) to afford th

Merging metal-organic framework catalysis with organocatalysis: A thiourea functionalized heterogeneous catalyst at the nanoscale

Luan, Yi,Zheng, Nannan,Qi, Yue,Tang, Jia,Wang, Ge

, p. 925 - 929 (2014)

A new thiourea-containing metal-organic framework (MOF) catalyst was synthesized. It overcomes recycling, self-aggregation and solvation issues that exist in homogeneous thiourea catalysts. Nanomorphology was introduced to increase the dispersion of the solid catalyst in solvent. Acetalization and Morita-Baylis-Hillman reactions were catalyzed using the new thiourea MOF catalyst. This journal is the Partner Organisations 2014.

Aqueous Baylis-Hillman reactions of cyclopent-2-enone using imidazole as catalyst

Luo, Sanzhong,Zhang, Baolian,He, Jiaqi,Janczuk, Adam,Wang, Peng G.,Cheng, Jin-Pei

, p. 7369 - 7371 (2002)

In aqueous media, imidazole was found to catalyse Baylis-Hillman reactions of cyclopent-2-enone with various aldehydes to afford the desired adducts with high yields.

Efficient Baylis-Hillman reactions promoted by mild cooperative catalysts and their application to catalytic asymmetric synthesis

Yamada, Yoichi M. A.,Ikegami, Shiro

, p. 2165 - 2169 (2000)

Baylis-Hillman reactions were promoted by mild cooperative catalysts of tributylphosphine with phenols such as (±)-1,1'-bi-2-naphthol (BINOL) in THF to give α-methylene-β-hydroxyalkanones in high yield. The reactions proceeded much faster in the presence

Vinyl Anion Equivalents. Part IV. Efficient Synthesis of 2-(1-Hydroxyalkyl)-2-cyclopenten-1-ones

Kusuda, Shinya,Ueno, Yoshio,Toru, Takeshi

, p. 2720 - 2724 (1993)

Aldol reactions of lithium enolates resulted from conjugate additions of tributylstannyllithium to 2-(phenylseleno)-2-cyclopenten-1-one provides 2-(1-hydroxyalkyl)-2-cyclopenten-1-ones in high yields.Significantly good 1, 4-asymmetric induction took place

Catalysis through Dynamic Spacer Installation of Multivariate Functionalities in Metal-Organic Frameworks

Cao, Chen-Chen,Chen, Cheng-Xia,Wei, Zhang-Wen,Qiu, Qian-Feng,Zhu, Neng-Xiu,Xiong, Yang-Yang,Jiang, Ji-Jun,Wang, Dawei,Su, Cheng-Yong

supporting information, p. 2589 - 2593 (2019/03/04)

We demonstrate herein a facile strategy to engineer versatile catalytically active coordination interspace in the same primitive metal-organic framework (MOF) for variable heterogeneous catalysis. Different functional ligands can be reversibly inserted into and removed from proto-LIFM-28 individually or successively to bring in single or binary catalytic sites for specific reactions and switch the parent MOF to multipurpose catalysts. Alcohol-oxidation, Knoevenagel-condensation, click, acetal, and Baylis-Hillman reactions are achievable through simple exchange of a single catalytic spacer, while sequential or stepwise reactions are designable via selective combination of two catalytic spacers with different functionalities, thus making proto-LIFM-28 a multivariate MOF for multiuse and economic catalysis.

METHOD FOR SYNTHESIZING NOVEL COMPOUNDS DERIVED FROM 3-HYDROXY-CYCLOPENTYL ACETIC ACID

-

Paragraph 0249; 0253; 0254; 0255, (2018/03/25)

The present invention relates to compounds of formula (I): in which R1 is a hydrogen atom, a phenyl radical, or a straight or branched, saturated or unsaturated hydrocarbon radical having 1 to 8 carbon atoms.

Dual Iminium- and Lewis Base Catalyzed Morita-Baylis-Hillman Reaction on Cyclopent-2-enone

Innocenti, Riccardo,Menchi, Gloria,Trabocchi, Andrea

supporting information, p. 820 - 824 (2017/12/26)

The application of iminium catalysis to the challenging Morita-Baylis-Hillman reaction on cyclopenten-2-one leads to the corresponding allylic alcohols in excellent yields. Experimental evidence shows that secondary amines act as co-catalysts activating t

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