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2-Azabicyclo[2.2.2]oct-7-ene-5-carboxylic acid, 4-(methoxymethoxy)-3-oxo-2-(phenylmethyl)-, (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenylethyl)cyclohexyl ester, (1R,4S,5S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

660849-26-3

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660849-26-3 Usage

Main Properties

1. Chemical Structure: Contains a heterocyclic ring system and a carboxylic acid functional group.
2. Functional Groups: Cyclohexyl ester, methyl, and phenylmethyl substituents.
3. Stereochemistry: Exhibits stereochemical configurations (1R,2S,5R) and (1R,4S,5S).
4. Complexity: Classified as a complex organic compound.
5. Potential Applications: Likely used in medicinal chemistry, possibly as a drug candidate or synthetic intermediate.

Specific Content

1. Name: 2-Azabicyclo[2.2.2]oct-7-ene-5-carboxylic acid, 4-(methoxymethoxy)-3-oxo-2-(phenylmethyl)-, (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenylethyl)cyclohexyl ester, (1R,4S,5S)
2. Structure: Contains a cyclohexyl ester group with methyl and phenylmethyl substituents, integrated into a complex heterocyclic ring system.
3. Stereochemistry: Configurations are designated as (1R,2S,5R) and (1R,4S,5S), indicating the arrangement of substituents around chiral centers.
4. Functional Groups: Includes a carboxylic acid functional group, as well as methoxy and keto groups.
5. Applications: Potential use in medicinal chemistry, either as a drug candidate or as a synthetic intermediate in pharmaceutical research. Further analysis and characterization are required to determine its specific properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 660849-26-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,0,8,4 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 660849-26:
(8*6)+(7*6)+(6*0)+(5*8)+(4*4)+(3*9)+(2*2)+(1*6)=183
183 % 10 = 3
So 660849-26-3 is a valid CAS Registry Number.

660849-26-3Relevant academic research and scientific papers

Synthesis and Evaluation as Glycosidase Inhibitors of Isoquinuclidines Mimicking a Distorted β-Mannopyranoside

Boehm, Matthias,Lorthiois, Edwige,Meyyappan, Muthuppalaniappan,Vasella, Andrea

, p. 3787 - 3817 (2007/10/03)

Racemic and enantiomerically pure manno-configured isoquinuclidines were synthesized and tested as glycosidase inhibitors. The racemic key isoquinuclidine intermediate was prepared in high yield by a cycloaddition (tandem Michael addition/aldolisation) of

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