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N-(tert-butyloxycarbonyl)-2-(4'-methoxyphenyl)-4,5,6-trihydro-piperidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1097200-75-3

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1097200-75-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1097200-75-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,7,2,0 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1097200-75:
(9*1)+(8*0)+(7*9)+(6*7)+(5*2)+(4*0)+(3*0)+(2*7)+(1*5)=143
143 % 10 = 3
So 1097200-75-3 is a valid CAS Registry Number.

1097200-75-3Relevant academic research and scientific papers

Cobalt-catalyzed arylation and alkenylation of alpha-bromo eneformamides and enecarbamates by cross-coupling with organic bromides: Application to the synthesis of functionalized piperidines and azepanes

Bassler, Daniel P.,Alwali, Amir,Spence, Laura,Beale, Oliver,Beng, Timothy K.

, p. 6 - 12 (2015)

The synthesis of α-arylated and alkenylated piperidine and azepane derivatives has been accomplished through cross-coupling of α-bromo eneformamides or enecarbamates with feedstock organic halides such as aryl and vinyl bromides, under cobalt catalysis. The coupling products, which themselves are synthetic intermediates for accessing other functionalized piperidines and azepanes are obtained in good to excellent yields.

Regioselectivity Influences in Platinum-Catalyzed Intramolecular Alkyne O-H and N-H Additions

Costello, Jeff P.,Ferreira, Eric M.

supporting information, p. 9934 - 9939 (2019/12/24)

The steric and electronic drivers of regioselectivity in platinum-catalyzed intramolecular hydroalkoxylation are elucidated. A branch point is found that divides the process between 5-exo and 6-endo selective processes, and enol ethers can be accessed in good yields for both oxygen heterocycles. The main influence arises from an electronic effect, where the alkyne substituent induces a polarization of the alkyne that leads to preferential heteroatom attack at the more electron-deficient carbon. The electronic effects are studied in other contexts, including hydroacyloxylation and hydroamination, and similar trends in directionality are predominant although not uniformly observed.

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