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tert-butyl N-benzyl(4-oxocyclohexyl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

188562-91-6

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188562-91-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 188562-91-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,5,6 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 188562-91:
(8*1)+(7*8)+(6*8)+(5*5)+(4*6)+(3*2)+(2*9)+(1*1)=186
186 % 10 = 6
So 188562-91-6 is a valid CAS Registry Number.

188562-91-6Relevant academic research and scientific papers

3-(dimethylaminomethyl) cyclohex-4-alcohol derivative as well as preparation method and pharmaceutical application thereof

-

, (2021/05/08)

The invention belongs to the field of pharmacy, and relates to a 3-(dimethylaminomethyl) cyclohex-4-alcohol derivative with a general formula (I) or a salt thereof and a preparation method, and relates to an application of the compound in treatment of opioid receptor mediated diseases. The present invention provides a pharmaceutically acceptable solvate or hydrate of a compound of formula (I), and also provides a pharmaceutical composition comprising: a compound of formula (I) or a pharmaceutically acceptable salt, solvate or hydrate thereof; and a pharmaceutically acceptable carrier. The medicine prepared from the compound can be used for treating or improving diseases related to an opioid receptor; wherein the diseases can be selected from but not limited to pain, gastrointestinal diseases and depression.

Synthesis of a series of polar, orthogonally protected, α,α-disubstituted amino acids

Yokum, T. Scott,Bursavich, Matthew G.,Piha-Paul, Sarina A.,Hall, David A.,McLaughlin, Mark L.

, p. 4013 - 4016 (2007/10/03)

The synthesis of four novel, 'cationic', α,α-disubstituted amino acids is described. The new amino acids use an orthogonal protection scheme making them suitable for incorporation via solid-phase peptide synthesis.

Synthesis of 2-azabicyclo[3.3.1]lnonanes by means of (carbamoyl)dichloromethyl radical cyclization

Quirante, Josefina,Escolano, Carmen,Massot, Mireia,Bonjoch, Josep

, p. 1391 - 1402 (2007/10/03)

A new procedure for the synthesis of 2-azabicyclo[3.3.1]nonanes by intramolecular carboradical cyclization of 4-(trichloroacetamido)cyclohexenes substituted with an electron withdrawing substituent tester or nitrile) is described. The procedure allows the preparation of synthetically interesting azabicyclos 14 and 15 in nearly 70% yield.

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