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Cyclohexanecarboxylic acid, 3-(3-butenyl)-2-oxo-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

127230-66-4

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127230-66-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127230-66-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,2,3 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 127230-66:
(8*1)+(7*2)+(6*7)+(5*2)+(4*3)+(3*0)+(2*6)+(1*6)=104
104 % 10 = 4
So 127230-66-4 is a valid CAS Registry Number.

127230-66-4SDS

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 ethyl 3-but-3-enyl-2-oxocyclohexane-1-carboxylate

1.2 Other means of identification

Product number -
Other names 3-But-3-enyl-2-oxo-cyclohexancarbonsaeure-aethylester

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:127230-66-4 SDS

127230-66-4Downstream Products

127230-66-4Relevant academic research and scientific papers

Synthesis of ABE tricyclic analogues of methyllycaconitine using a Wacker oxidation-aldol strategy to append the B ring to the AE fragment

Barker, David,Brimble, Margaret A.,McLeod, Malcolm,Savage, G. Paul,Wong, David J.

, p. 924 - 931 (2002)

The synthesis of ABE tricyclic analogues 18 of the alkaloid methyllycaconitine 1 is described. The analogues contain the key pharmacophore reputed to be responsible for the biological activity of methyllycaconitine 1, namely, a homocholine motif formed fr

Selective inhibitors of the serine protease plasmin: Probing the S3 and S3′ subsites using a combinatorial library

Xue, Fengtian,Seto, Christopher T.

, p. 6908 - 6917 (2007/10/03)

A combinatorial library of 400 serine protease inhibitors with the general structure Cbz-Xaa-Trp-cyclohexanone-Trp-Yaa-OH has been constructed. The library was synthesized on the solid phase using mix-and-split synthesis, where 20 di

Manganese(III)-Based Oxidative Free-Radical Cyclization of Unsaturated β-Keto Esters, 1,3-Diketones, and Malonate Diesters

Kates, Steven A.,Dombroski, Mark A.,Snider, Barry B.

, p. 2427 - 2436 (2007/10/02)

Oxidative free-radical cyclizations of unsaturated β-keto esters, 1,3-diketones, and malonate diesters with 2 equiv of Mn(OAc)3*2H2O and 1 equiv of Cu(OAc)2*H2O are described.Oxidation of β-keto ester 1 with Mn(III) to enol radical 2 followed by 6-exo cyc

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