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1-(1-Cyclohexenyl)-3-ethoxy-2-propanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51149-72-5

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51149-72-5 Usage

Type of compound

Ketone

Structural features

a. Cyclohexenyl ring
b. Ethoxy group attached to the carbon chain

Common uses

a. Synthesis of various organic compounds
b. Building block for more complex molecules
c. Fragrance and flavor industry
d. Production of pharmaceuticals
e. Agricultural chemicals

Odor

Sweet, fruity

Stability

Relatively stable under normal storage conditions

Safety precautions

a. Potential skin and eye irritant
b. Handle with care

Check Digit Verification of cas no

The CAS Registry Mumber 51149-72-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,4 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51149-72:
(7*5)+(6*1)+(5*1)+(4*4)+(3*9)+(2*7)+(1*2)=105
105 % 10 = 5
So 51149-72-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H18O2/c1-2-13-9-11(12)8-10-6-4-3-5-7-10/h6H,2-5,7-9H2,1H3

51149-72-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(cyclohexen-1-yl)-3-ethoxypropan-2-one

1.2 Other means of identification

Product number -
Other names 2-Propanone,1-(1-cyclohexen-1-yl)-3-ethoxy

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:51149-72-5 SDS

51149-72-5Downstream Products

51149-72-5Relevant academic research and scientific papers

Catalytic Role of Copper Triflate in Lewis Acid Promoted Reactions of Diazo Compounds

Doyle, Michael P.,Trudell, Mark L.

, p. 1196 - 1199 (2007/10/02)

Copper(II)trifluoromethanesulfonate is often a superior catalyst for transformations of diazo compounds that are normally promoted by boron trifluoride etherate.Formal carbon-oxygen insertion occurs when ortho esters are reacted with diazocarbonyl compounds in the presence of Cu(OTf)2, although the use of BF3*Et2O provides higher yields of insertion products.In contrast, the β,γ-unsaturated diazo ketone 6 undergoes intramolecular cyclization to produce the corresponding cyclopentenone in higher yield with Cu(OTf)2 catalysis than with the use of BF3*Et2O.Intamolecular cyclopropanation of the γ,δ-unsaturated diazo ketone 8 occurs in exceptionally high yield in the presence of Cu(OTf)2, whereas with BF3*Et2O intramolecular cyclization occurs with extensive rearrangement anf fluoride transfer.Copper(II)triflate is unique among transition-metal catalysts that are normally employed for reactions with diazo compounds in its effectiveness for these transformations.

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