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3-Cyclohexen-1-ol, 2,2,4-trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81452-72-4

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81452-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81452-72-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,4,5 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 81452-72:
(7*8)+(6*1)+(5*4)+(4*5)+(3*2)+(2*7)+(1*2)=124
124 % 10 = 4
So 81452-72-4 is a valid CAS Registry Number.

81452-72-4Downstream Products

81452-72-4Relevant academic research and scientific papers

A study of epoxyolefin cyclizations catalyzed by bismuth trifluoromethanesulfonate and other metal triflates

Lacey, Joshua R.,Anzalone, Peter W.,Duncan, Christopher M.,Hackert, Matthew J.,Mohan, Ram S.

, p. 8507 - 8511 (2007/10/03)

Epoxyolefin cyclizations have attracted considerable interest due to their importance in biosynthetic pathways. Bismuth trifluoromethanesulfonate as well as several other metal triflates are shown to be highly effective (0.1 mol %) catalysts for the cycli

Glycinoeclepins, Natural Hatching Stimuli for the Soybean Cyst Nematode, Heterodera Glycines. II. Structural Elucidation

Masamune, Tadashi,Fukuzawa, Akio,Furusaki, Akio,Ikura, Mitsuhiko,Matsue, Hideki,et al.

, p. 1001 - 1014 (2007/10/02)

The structures of three new compounds, glycinoeclepsins A, B, and C, isolated from the hatch-stimulating extracts of kidney beans for the soybean cyst nematode, have been determined.The structures were resolved by using spectroscopic methods, especially b

Preparation of 2-exo-Hydroxy-7-oxabicyclo[2.2.1]heptanes

-

, (2008/06/13)

2-exo-Hydroxy-7-oxabicyclo[2.2.1]heptanes are prepared by treating the corresponding cis-epoxycyclohexanol with acid in an inert solvent or by treating a 3-cyclohexen-1-ol which will produce the corresponding cis-epoxy alcohol successively or concurrently with an oxidizing agent and an acid in an inert solvent.

CYCLOHEXENOL ANNULATION VIA THE ALKOXY-ACCELERATED REARRANGEMENT OF VINYLCYCLOBUTANES

Danheiser, Rick L.,Martinez-Davila, Carlos,Sard, Howard

, p. 3943 - 3950 (2007/10/02)

The lithium and potassium salts of 2-vinylcyclobutanols undergo vinylcyclobutane rearrangement at 25-70 gradC, providing an efficient method for the synthesis of 3-cyclohexenol derivatives. 2-Vinylcyclobutanones are prepared from α,β-unsaturated carbonyl

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