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1-(4-bromophenyl)hex-5-en-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71434-58-7

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71434-58-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71434-58-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,4,3 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 71434-58:
(7*7)+(6*1)+(5*4)+(4*3)+(3*4)+(2*5)+(1*8)=117
117 % 10 = 7
So 71434-58-7 is a valid CAS Registry Number.

71434-58-7Relevant academic research and scientific papers

Cyclopentane Formation from Flexible Precursors Using Samarium(II) Reagents

Aretz, Christopher D.,Escobedo, Humberto,Cowen, Bryan J.

supporting information, p. 1880 - 1884 (2018/05/09)

Three efficient methods for five-membered ring carbocycle synthesis have been developed from simple starting materials using samarium(II) reagents. A Reformatsky aldol reaction proceeded efficiently with samarium(II) iodide using lithium bromide as an additive. A new intramolecular alkylation of a samarium enolate was realized with a pendant sulfonate ester leaving group. Pinacol cyclization of a simple diketone was also demonstrated giving a diol product in high stereoselectivity. A promising lead result has been established demonstrating enantioselectivity in a chiral ligand controlled Reformatsky aldol reaction.

Anti-Markovnikov Hydrofunctionalization of Alkenes: Use of a Benzyl Group as a Traceless Redox-Active Hydrogen Donor

Lonca, Geoffroy Hervé,Ong, Derek Yiren,Tran, Thi Mai Huong,Tejo, Ciputra,Chiba, Shunsuke,Gagosz, Fabien

supporting information, p. 11440 - 11444 (2017/09/11)

A protocol for the anti-Markovnikov hydrofunctionalization of alkenes has been developed by the use of a benzyl group as a traceless redox-active hydrogen donor. Under copper catalysis and in the presence of CF3- or N3-containing hyp

Diastereoselective C?H Bond Amination for Disubstituted Pyrrolidines

Iovan, Diana A.,Wilding, Matthew J. T.,Baek, Yunjung,Hennessy, Elisabeth T.,Betley, Theodore A.

supporting information, p. 15599 - 15602 (2017/11/16)

We report herein the improved diastereoselective synthesis of 2,5-disubstituted pyrrolidines from aliphatic azides. Experimental and theoretical studies of the C?H amination reaction mediated by the iron dipyrrinato complex (AdL)FeCl(OEt2) provided a model for diastereoinduction and allowed for systematic variation of the catalyst to enhance selectivity. Among the iron alkoxide and aryloxide catalysts evaluated, the iron phenoxide complex exhibited superior performance towards the generation of syn 2,5-disubstituted pyrrolidines with high diastereoselectivity.

Discovery of biphenylketones as dual modulators of inflammation and bone loss

Greig, Iain R.,Coste, Emmanuel,Ralston, Stuart H.,Van'T Hof, Rob J.

supporting information; experimental part, p. 5548 - 5551 (2010/12/29)

Biphenylketones were identified as novel inhibitors of NFκB activation. Structure-activity studies led to the identification of compound 4c, which had good potency against osteoclasts (IC50 = 0.8 μM), showed oral activity, and was able to compl

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