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2-Cyclohexene-1-carboxaldehyde, 1-methyl-4-oxo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54125-08-5

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54125-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54125-08-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,2 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 54125-08:
(7*5)+(6*4)+(5*1)+(4*2)+(3*5)+(2*0)+(1*8)=95
95 % 10 = 5
So 54125-08-5 is a valid CAS Registry Number.

54125-08-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-4-oxocyclohex-2-ene-1-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2-Cyclohexene-1-carboxaldehyde,1-methyl-4-oxo

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:54125-08-5 SDS

54125-08-5Relevant academic research and scientific papers

Evaluation of alkene isomerization as a trigger for enediyne activation

Semmelhack,Sarpong, Richmond,Bergman, Jeffrey,Ho, Douglas M.

, p. 541 - 544 (2007/10/03)

The concept of non-conjugated-to-conjugated double bond isomerization as a triggering mechanism for a calicheamicin model was tested. A bicyclo[7.3.1] enediyne framework was prepared with a bridgehead double bond and an acetonyl side chain. Base-promoted exchange failed to produce the conjugated isomer. Computational analysis suggested that additional conjugating groups would favor the isomerization, but experiment proved that not to be correct.

Lewis acid catalyzed procedure for selective conversion of the carbocyclic Diels-Alder adducts of Danishefsky's diene to 2-cyclohexenones and its extension to their one-pot syntheses

Inokuchi,Okano,Miyamoto,Bte Madon,Takagi

, p. 1549 - 1552 (2007/10/03)

Conversion of the carbocyclic Diels-Alder adducts of 4-methoxy-2-trimethylsiloxy-1,3-butadiene (Danishefsky's diene), prepared by heating, to the corresponding 2-cyclohexenones was performed cleanly by use of Lewis acids such as Yb(OTf)3 and Bu

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