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2-Cyclohexen-1-one, 5,5-dimethyl-3-(2-propynyloxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

877823-42-2

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877823-42-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 877823-42-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,7,8,2 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 877823-42:
(8*8)+(7*7)+(6*7)+(5*8)+(4*2)+(3*3)+(2*4)+(1*2)=222
222 % 10 = 2
So 877823-42-2 is a valid CAS Registry Number.

877823-42-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,5-dimethyl-3-(prop-2-ynyloxy)cyclohex-2-enone

1.2 Other means of identification

Product number -
Other names 3-(prop-2-ynyloxy)cyclohex-2-enone

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:877823-42-2 SDS

877823-42-2Relevant academic research and scientific papers

Zinc-mediated alkylation and acylation of 1,3-dicarbonyl compounds

Yadav,Reddy, B. V. Subba,Mishra, Anand Kumar

experimental part, p. 280 - 281 (2010/09/05)

1,3-Dicarbonyl compounds undergo smooth allylation, benzylation, propargylation, and acylation with halides using metallic zinc in DMF at 60 °C to afford the corresponding allyl, benzyl, 2-propynyl, and acylated 1,3-diesters in good yields. In the case of cyclic 1,3-diketones, the corresponding enol ethers are obtained as sole products instead of C-alkylation.

Iron(III) tosylate in the preparation of dimethyl and diethyl acetals from ketones and β-keto enol ethers from cyclic β-diketones

Mansilla, Horacio,Afonso, Maria M.

, p. 2607 - 2618 (2008/12/22)

An efficient method for conversion of ketones to their corresponding dimethyl and diethyl acetals and of cyclic β-diketones into β-keto enol ethers using Fe(OTs)3 as a catalyst is described. Copyright Taylor & Francis Group, LLC.

Formation of bicyclic pyrroles and furans through an enone allene photocycloaddition and fragmentation sequence

Lutteke, Ginger,Alhussainy, Rana,Wrigstedt, Pauli J.,Hue, B. T. Buu,De Gelder, Rene,Van Maarseveen, Jan H.,Hiemstra, Henk

experimental part, p. 925 - 933 (2009/04/04)

The [2+2] photocycloaddition of allenes 15-18, 23 and 26 was studied. Irradiation of a solution of these substrates in acetonitrile at 300 nm resulted in the clean conversion of the starting materials into a mixture of photoproducts. The major product in

Cerium(IV) ammonium nitrate-catalyzed synthesis of β-keto enol ethers from cyclic β-diketones and their deprotection

Banerjee, Biplab,Mandal, Samir Kumar,Roy, Subhas Chandra

, p. 16 - 17 (2007/10/03)

A mild and efficient method for etherification of cyclic β-diketones with alcohols has been developed using a catalytic amount of cerium(IV) ammonium nitrate at room temperature to afford the corresponding β-keto enol ethers in good to excellent yields. The deprotections of enol ethers in water-acetonitrile (1:1) using a catalytic amount (10 mol %) of cerium(IV) ammonium nitrate have also been achieved. Copyright

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