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2-Propanone, 1-(3,4-diethoxyphenyl)-, oxime, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104886-63-7

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104886-63-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104886-63-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,8,8 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104886-63:
(8*1)+(7*0)+(6*4)+(5*8)+(4*8)+(3*6)+(2*6)+(1*3)=137
137 % 10 = 7
So 104886-63-7 is a valid CAS Registry Number.

104886-63-7SDS

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 (E)-1-(3,4-diethoxyphenyl)-2-propanone oxime

1.2 Other means of identification

Product number -
Other names (3,4-diethoxy-phenyl)-acetone oxime

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:104886-63-7 SDS

104886-63-7Downstream Products

104886-63-7Relevant academic research and scientific papers

The Palladium Assisted Transfer Reduction of α,β-Unsaturated Nitroalkenes to Oximes Using Ammonium Formate

Kabalka, George W.,Pace, R. David,Wadgaonkar, P.P.

, p. 2453 - 2458 (2007/10/02)

α,β-Unsaturated nitroalkenes are readily reduced to the corresponding oximes in good yields using ammonium formate in the presence of palladium.The reactions occur rapidly at room temperature in a solvent system of methanol and tetrahydrofuran.

THE PALLADIUM ASSISTED TRANSFER REDUCTION OF α,β-UNSATURATED NITROALKENES USING SODIUM HYPOPHOSPHITE: A SYNTHESIS OF OXIMES

Varma, Rajender S.,Varma, Manju,Kabalka, George W.

, p. 91 - 96 (2007/10/02)

α,β-Unsaturated nitroalkenes are readily reduced by sodium hypophosphite to the corresponding oximes in the presence of palladium.

STANNOUS CHLORIDE REDUCTION OF α,β-UNSATURATED NITROALKENES : A DIRECT SYNTHESIS OF 2-ARYL-2H-1-BENZOPYRAN-3(4H)-ONE OXIMES

Varma, Rajender S.,Varma, Manju,Gai, Yuan-Zhu,Kabalka, George W.

, p. 2581 - 2586 (2007/10/02)

Stannous chloride, in acetone, readily reduced the α,β-unsaturated nitroalkenes to the cprresponding oximes at the room temperature.A series of 2-aryl-3-chromanone oximes were obtained via the reduction of 3-nitrochromenes.

A FACILE KETOXIME PREPARATION VIA THE REDUCTION OF Αa,β-UNSATURATED NITROALKENES USING SODIUM STANNITE

Varma, Rajender S.,Varma, Manju,Kabalka, George W.

, p. 6013 - 6014 (2007/10/02)

α,β-Unsaturated nitroalkenes are readily reduced by sodium stannite to ketoximes at room temperature.

CHROMIUM(II) CHLORIDE REDUCTION OF β-ARYL, α,β-UNSATUTARED NITROALKENES. A FACILE ROUTE TO OXIMES

Varma, Rajender S.,Varma, Manju,Kabalka, George W.

, p. 1325 - 1332 (2007/10/02)

α,β-Unsaturated nitroalkenes are rapidly reduced by chromium(II) chloride to oximes.

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