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ethyl 4-(4-methoxybenzyloxy)-3-oxobutanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

727382-81-2

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727382-81-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 727382-81-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,7,3,8 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 727382-81:
(8*7)+(7*2)+(6*7)+(5*3)+(4*8)+(3*2)+(2*8)+(1*1)=182
182 % 10 = 2
So 727382-81-2 is a valid CAS Registry Number.

727382-81-2SDS

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 ethyl 4-(4-methoxybenzyloxy)-3-oxobutanoate

1.2 Other means of identification

Product number -
Other names ethyl 4-(4-methoxybenzyloxy)-3-oxobutyrate

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:727382-81-2 SDS

727382-81-2Relevant academic research and scientific papers

A Stereoselective Synthesis of the Carbon Backbone of Phoslactomycin B

Raghavan, Sadagopan,Patel, Javed Sardar

, p. 2981 - 2997 (2017/06/06)

A convergent synthesis of the entire carbon framework of phoslactomycin B is disclosed. An initial route aimed to create the C-8 tetrasubstituted stereocentre through regioselective intermolecular coupling between an internal alkyne and an allyl silyl ether, adopting Trost's protocol, followed by [2,3] sigmatropic rearrangement. But this was not successful. In a second approach, a propargylic sulfide was rearranged to give an unsaturated ketone. This was then treated with lithio acetonitrile to create the C-8 stereocentre selectively. The C-4 and C-5 stereocentres were introduced by a non-Evans syn-aldol reaction using Crimmins's protocol. The C-9 and C-11 carbinol centres were created by asymmetric transfer hydrogenation. The (Z,Z)-diene moiety was introduced by partial reduction of a diyne following Hansen's modification of the Boland reduction reaction.

Synthesis of indolequinones from bromoquinones and enamines mediated by Cu(OAc)2H2O

Inman, Martyn,Moody, Christopher J.

supporting information; experimental part, p. 6023 - 6026 (2010/11/20)

A Cu(II)-mediated synthesis of indolequinones from the corresponding bromoquinones and enamines is reported. The key oxidative cyclization proceeds in good yield for a broad range of substrates and can be performed on a multigram scale, allowing access to biologically interesting structures.

Pyrid-2-one derivatives and methods of use

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Page 44, (2010/02/07)

Selected compounds are effective for treatment of diseases, such as cell proliferation or apoptosis mediated diseases. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable derivatives thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving stroke, cancer and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.

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