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1-((4-tert-butylcyclohexylidene)methyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

150736-86-0

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150736-86-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 150736-86-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,7,3 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 150736-86:
(8*1)+(7*5)+(6*0)+(5*7)+(4*3)+(3*6)+(2*8)+(1*6)=130
130 % 10 = 0
So 150736-86-0 is a valid CAS Registry Number.

150736-86-0Relevant academic research and scientific papers

Reduction of titanocene dichloride with dysprosium: Access to a stable titanocene(II) equivalent for phosphite-free Takeda carbonyl olefination

Bousrez,Déchamps,Vasse,Jaroschik

, p. 9359 - 9362 (2015/06/16)

The reduction of titanocene dichloride with dysprosium yields a new titanocene(ii) equivalent without the need for further stabilising ligands. This reagent can be employed in combination with dithioacetals for the olefination of different carbonyl groups and allows for a simplified all-in-one procedure.

Conformational and structural analysis of exocyclic olefins and ketimines by multinuclear magnetic resonance

Montalvo-Gonzalez, Ruben,Montalvo-Gonzalez, J. Ascencion,Ariza-Castolo, Armando

experimental part, p. 907 - 912 (2009/05/09)

The 1H, 13C, and 15N NMR spectra of 5 exocyclic alkenes and 15 different ketimines obtained from cyclohexanone and derivatives using benzyl bromide and primary amines - are analyzed. Relative stereochemical and preferentia

3,5-Bis(trifluoromethyl)phenyl sulfones in the Julia-Kocienski olefination - Application to the synthesis of tri- and tetrasubstituted olefins

Alonso, Diego A.,Fuensanta, Monica,Najera, Carmen

, p. 4747 - 4754 (2007/10/03)

3,5-Bis(trifluoromethyl)phenyl (BTFP) sulfones 8a-d are successfully employed in the modified Julia olefination reaction with carbonyl compounds employing phosphazene base P4-tBu at room temp. in THF, affording tri- and tetrasubstituted olefins in good yi

EFFICIENT OLEFINATION WITH α-ALKYL CYCLIC PHOSPHONAMIDES

Hanessian, Stephen,Bennani, Youssef L.,Leblanc, Yves

, p. 1411 - 1424 (2007/10/02)

A variety of acyclic and cyclic aldehydes and ketones can be converted into the corresponding alkylidene, benzylidene and methoxycarbonyl alkylidene derivatives by treatment with 1,3,2-diazaphospholidine-2-alkyl-1,3-dimethyl 2-oxides (α-alkyl cyclic phosphonamides) under mild conditions.This olefination method is particularly useful in the case of enolizable carbonyl compounds.

Preparation, Alkylation Reactions, and Conformational Analysis of Esters of Phospholanic Acid. Preparation and Reactivity of (2S*,5S*)-1,2,5-Tribenzyl-1-oxophospholane

Polniaszek, Richard P.,Foster, Alvie L.

, p. 3137 - 3146 (2007/10/02)

Optimum conditions for the reaction of 1,4-butanediylmagnesium dibromide and alkyl phosphorodichloridates are described.The general geometric requirements of the cyclization reaction transition state are discussed.Alkylation reactions of phospholanate est

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