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3048-85-9

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3048-85-9 Usage

Bicyclic compound

Contains a fused ring system

Carboxylic acid groups

Two present in the structure

Ethoxycarbonyl group

Attached to one of the carboxylic acid groups, also known as the ethyl ester

Potential applications

Organic synthesis and medicinal chemistry

Building block

Can be used for the synthesis of other complex organic molecules

Precursor

For the development of pharmaceuticals

Biological activities

May have potential biological activities of interest for further research and development

Versatility

Diverse potential applications due to its unique structure and functional groups

Check Digit Verification of cas no

The CAS Registry Mumber 3048-85-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,4 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3048-85:
(6*3)+(5*0)+(4*4)+(3*8)+(2*8)+(1*5)=79
79 % 10 = 9
So 3048-85-9 is a valid CAS Registry Number.

3048-85-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethoxycarbonylbicyclo[2.2.2]octane-2,3-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names 1-(ethoxycarbonyl)bicyclo[2.2.2]octane-2,3-dicarboxylic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3048-85-9 SDS

3048-85-9Relevant articles and documents

Carbon chain shape selectivity by the mouse olfactory receptor OR-I7

Liu, Min Ting,Ho, Jianghai,Liu, Jason Karl,Purakait, Radhanath,Morzan, Uriel N.,Ahmed, Lucky,Batista, Victor S.,Matsunami, Hiroaki,Ryan, Kevin

supporting information, p. 2541 - 2548 (2018/04/12)

The rodent OR-I7 is an olfactory receptor exemplar activated by aliphatic aldehydes such as octanal. Normal alkanals shorter than heptanal bind OR-I7 without activating it and hence function as antagonists in vitro. We report a series of aldehydes designed to probe the structural requirements for aliphatic ligand chains too short to meet the minimum approximate 6.9 ? length requirement for receptor activation. Experiments using recombinant mouse OR-I7 expressed in heterologous cells show that in the context of short aldehyde antagonists, OR-I7 prefers binding aliphatic chains without branches, though a single methyl on carbon-3 is permitted. The receptor can accommodate a surprisingly large number of carbons (e.g. ten in adamantyl) as long as the carbons are part of a conformationally constrained ring system. A rhodopsin-based homology model of mouse OR-I7 docked with the new antagonists suggests that small alkyl branches on the alkyl chain sterically interfere with the hydrophobic residues lining the binding site, but branch carbons can be accommodated when tied back into a compact ring system like the adamantyl and bicyclo[2.2.2]octyl systems.

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