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7-((tert-butyldiphenylsilyl)oxy)-2-methylhept-1-en-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

134792-73-7

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134792-73-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134792-73-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,7,9 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 134792-73:
(8*1)+(7*3)+(6*4)+(5*7)+(4*9)+(3*2)+(2*7)+(1*3)=147
147 % 10 = 7
So 134792-73-7 is a valid CAS Registry Number.

134792-73-7Relevant academic research and scientific papers

Diastereoselective Synthesis of Highly Substituted Tetrahydrofurans by Pd-Catalyzed Tandem Oxidative Cyclization-Redox Relay Reactions Controlled by Intramolecular Hydrogen Bonding

Brooks, Joshua L.,Xu, Liping,Wiest, Olaf,Tan, Derek S.

, p. 57 - 75 (2017/04/26)

Palladium-catalyzed oxidative cyclization of alkenols provides a convenient entry into cyclic ethers but typically proceeds with little or no diastereoselectivity for cyclization of trisubstituted olefins to form tetrahydrofurans due to the similar energi

Initiating radical cyclizations by H{radical dot} transfer from transition metals

Hartung, John,Pulling, Mary E.,Smith, Deborah M.,Yang, David X.,Norton, Jack R.

experimental part, p. 11822 - 11830 (2009/04/11)

CpCr(CO)3H and HV(CO)4(P-P) (where P-P is a chelating diphosphine) can be used to initiate radical cyclizations by transferring H{radical dot} to activated terminal olefins. CpCr(CO)3H can catalyze reductive cyclizations,

Substituent control in the synthesis of tetrahydropyrans, oxepanes and oxocanes by episulphonium ion-mediated cyclisation

Lopez-Tudanca,Jones,Brownbridge

, p. 2261 - 2264 (2007/10/02)

Cyclisation of the heptenols (1), (6a), (6b), and (6c) to cyclic ethers via episulphonium ions has been studied and the effect of allylic substituents on the size of ring produced has been explored.

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