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Ethanone, 1-phenyl-2-(tetrahydro-2H-pyran-2-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22528-77-4

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22528-77-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22528-77-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,5,2 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22528-77:
(7*2)+(6*2)+(5*5)+(4*2)+(3*8)+(2*7)+(1*7)=104
104 % 10 = 4
So 22528-77-4 is a valid CAS Registry Number.

22528-77-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-2-(tetrahydro-2H-pyran-2-yl)-1-ethanone

1.2 Other means of identification

Product number -
Other names 1-phenyl-2-(tetrahydropyran-2-yl)ethanone

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:22528-77-4 SDS

22528-77-4Relevant academic research and scientific papers

Visible-light-promoted oxidative coupling of styrene with cyclic ethers

Kibriya, Golam,Ghosh, Debashis,Hajra, Alakananda

, p. 42 - 46 (2019/11/11)

A new visible-light-promoted oxidative coupling of vinylarenes with cyclic ethers has been developed using rose bengal as photocatalyst and tert-butyl hydrogenperoxide (TBHP) as oxidant under ambient air at room temperature. A library of α-oxyalkylated ketones with broad functionalities has been synthesized in moderate to good yields. A radical mechanism is suggested for the present protocol.

Organocatalytic Enantioselective Cycloetherifications Using a Cooperative Cation-Binding Catalyst

Jadhav, Amol P.,Oh, Jeong-A,Hwang, In-Soo,Yan, Hailong,Song, Choong Eui

supporting information, p. 5319 - 5322 (2018/09/13)

A highly enantioselective cycloetherification strategy for the straightforward synthesis of enantioenriched tetrahydrofurans, tetrahydropyrans, and oxepanes using Song's cation-binding oligoEG catalyst and KF as the base is demonstrated. A wide range of ?

Transition-Metal-Free Oxidative Decarboxylative Cross Coupling of α,β-Unsaturated Carboxylic Acids with Cyclic Ethers under Air Conditions: Mild Synthesis of α-Oxyalkyl Ketones

Ji, Peng-Yi,Liu, Yu-Feng,Xu, Jing-Wen,Luo, Wei-Ping,Liu, Qiang,Guo, Can-Cheng

, p. 2965 - 2971 (2017/03/23)

A novel K2S2O8-promoted decarboxylative cross coupling of α,β-unsaturated carboxylic acids with cyclic ethers was developed under aerobic conditions. The present protocol, which includes C-C and C=O bond formation in one s

Method of decarboxylation oxidative coupling for [alpha], [beta]-unsaturated carboxylic acid and cyclic ether compound

-

Paragraph 0184; 0203; 0204; 0205; 0206, (2017/08/27)

The invention discloses a method of decarboxylation oxidative coupling for [alpha], [beta]-unsaturated carboxylic acid and a cyclic ether compound. In the method, under an oxygen-containing atmosphere, the [alpha], [beta]-unsaturated carboxylic acid and t

Method for performing decarboxylated oxidative coupling on cinnamic acid derivatives and cyclic ethers

-

Paragraph 0153, (2017/08/27)

The invention discloses a method for performing decarboxylated oxidative coupling on cinnamic acid derivatives and cyclic ethers. The method comprises the step of carrying out a one-pot reaction between the cinnamic acid derivatives and cyclic ethers in a

MnO2-Catalyzed Oxidative Alkylation of Enamides with Ethers via C(sp3)-H/C(sp2)-H Cross-Dehydrogenative Coupling and Hydrolysis Sequence

Hu, Zhiyan,Tang, Yucai,Zhang, Shan,Li, Xiaoqing,Du, Xiaohua,Xu, Xiangsheng

, p. 2557 - 2560 (2015/11/11)

A new MnO2-catalyzed oxidative alkylation of enamides with a C(sp3)-H bond adjacent to an oxygen atom is described. This method achieves a C(sp3)-H/C(sp2)-H cross-dehydrogenative coupling and hydrolysis, thus pr

Gold(I)/(III)-catalyzed synthesis of cyclic ethers; Valency-controlled cyclization modes

Morita, Nobuyoshi,Yasuda, Arisa,Shibata, Motohiro,Ban, Shintaro,Hashimoto, Yoshimitsu,Okamoto, Iwao,Tamura, Osamu

supporting information, p. 2668 - 2671 (2015/06/16)

Strategic use of oxophilic (hard) gold(III) and π-philic (soft) gold(I) catalysts provides access to two types of cyclic ethers from propargylic alcohols. Thus, heating propargylic alcohols with an oxophilic gold(III) catalyst (AuBr3) results i

Oxa-Michael addition promoted by the aqueous sodium carbonate

Guo, Shi-Huan,Xing, Sheng-Zhu,Mao, Shuai,Gao, Ya-Ru,Chen, Wen-Liang,Wang, Yong-Qiang

supporting information, p. 6718 - 6720 (2014/12/11)

An efficient Michael addition of alcohols to activated alkenes promoted by sodium carbonate with water as reaction medium has been developed. The reaction provides a general, economical and environmentally friendly approach for the synthesis of β-alkoxycarbonyl compounds.

Tandem nucleophilic addition/oxa-michael reaction for the synthesis of cis-2,6-disubstituted tetrahydropyrans

Gharpure, Santosh J.,Prasad,Bera, Kalisankar

, p. 3570 - 3574 (2014/06/23)

A Lewis acid catalyzed tandem nucleophilic addition/oxa-Michael reaction was developed for the synthesis of cis-2,6-disubstituted tetrahydropyran (THP) derivatives in good yields with excellent diastereoselectivities. The strategy was successfully used in the construction of THP derivatives with three stereocenters in a highly stereoselective fashion. Copyright

Copper-catalyzed dehydrogenative cross-coupling reaction between unactivated ethers and simple ketones mediated by pyrrolidine

Huang, Xing-Fen,Zhu, Zhi-Qiang,Huang, Zhi-Zhen

, p. 8579 - 8582 (2013/09/12)

A copper-catalyzed dehydrogenative cross-coupling reaction between unactivated ethers and simple ketones mediated by pyrrolidine has been developed. Under the catalysis of CuBr2 and in the presence of pyrrolidine, either tetrahydrofuran 2a or tetrahydropyran 2b can react smoothly with a series of methyl aryl ketones 1a-m to give desired coupling products 3aa-mb using TBHP as an oxidant. The advantages of the dehydrogenative cross-coupling reaction are adoption of unmodified ethers as substrates, good tolerance of many functional groups and use of cheap copper salt as a catalyst. A plausible radical mechanism through enamine attack is proposed.

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