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2,5-Diazabicyclo[2.2.2]octane-3,6-dione,2,4-dimethyl-1-(1-methylethyl)-,(1S,4R)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

817575-48-7

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817575-48-7 Usage

Molecular structure

2,5-Diazabicyclo[2.2.2]octane-3,6-dione,2,4-dimethyl-1-(1-methylethyl),(1S,4R)-(9CI) has a complex molecular structure consisting of a bicyclic ring system with two nitrogen atoms, a carbonyl group, and two methyl groups and an isopropyl group attached to the ring.

Chirality

The compound is chiral, meaning it has a non-superimposable mirror image.

Classification

It is classified as a bicyclic guanidine.

Usage in organic synthesis

The compound is used as a catalyst in organic synthesis.

Application in pharmaceutical industry

It is used in the pharmaceutical industry for the preparation of various drugs.

Value in research

Its unique structure and properties make it a valuable compound in the fields of chemistry and pharmaceutical research.

Check Digit Verification of cas no

The CAS Registry Mumber 817575-48-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,7,5,7 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 817575-48:
(8*8)+(7*1)+(6*7)+(5*5)+(4*7)+(3*5)+(2*4)+(1*8)=197
197 % 10 = 7
So 817575-48-7 is a valid CAS Registry Number.

817575-48-7Upstream product

817575-48-7Downstream Products

817575-48-7Relevant academic research and scientific papers

Design and synthesis of novel type VI-like β-turn mimetics. Diversity at the i+1 and the i+2 position

De Borggraeve, Wim M.,Verbist, Bie M.P.,Rombouts, Frederik J.R.,Pawar, Vijaykumar G.,Smets, Wim J.,Kamoune, Laila,Alen, Jo,Van Der Eycken, Erik V.,Compernolle, Frans,Hoornaert, Georges J.

, p. 11597 - 11612 (2004)

In this paper, a synthetic approach for functionalised 5-aminopiperidinone- 2-carboxylate (APC) systems as non-pro cis-peptide bond containing external β-turn mimics is presented. The scope and limitations of the synthetic method are discussed and the pot

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