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Ethyl 6-oxo-2-azabicyclo[2.2.2]octane-2-carboxylate is a complex organic compound with the chemical formula C10H15NO3. It is a white crystalline solid that is soluble in organic solvents. ethyl 6-oxo-2-azabicyclo[2.2.2]octane-2-carboxylate is a derivative of 2-azabicyclo[2.2.2]octane, a bicyclic amine with a nitrogen atom in the ring structure. The "6-oxo" part of the name indicates the presence of a carbonyl group (C=O) at the 6th position in the bicyclic structure. The "carboxylate" ending signifies the presence of a carboxylate group (-COO-) attached to the molecule. Ethyl 6-oxo-2-azabicyclo[2.2.2]octane-2-carboxylate is used as an intermediate in the synthesis of various pharmaceuticals and other organic compounds due to its unique structural features and reactivity.

3885-76-5

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3885-76-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3885-76-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,8 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3885-76:
(6*3)+(5*8)+(4*8)+(3*5)+(2*7)+(1*6)=125
125 % 10 = 5
So 3885-76-5 is a valid CAS Registry Number.

3885-76-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 6-oxo-2-azabicyclo[2.2.2]octane-2-carboxylate

1.2 Other means of identification

Product number -
Other names N-Carbethoxydioscoron

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:3885-76-5 SDS

3885-76-5Downstream Products

3885-76-5Relevant academic research and scientific papers

Synthesis and pharmacology of isoquinuclidine derivatives as 5-HT3 ligands

Iriepa, Isabel,Villasante, Francisco J.,Galvez, Enrique,Labeaga, Luis,Innerarity, Ana,Orjales, Aurelio

, p. 189 - 192 (2007/10/03)

A series of 4-amino-5-chloro-2-methoxybenzoates and benzamides containing the 5- and 6-isoquinuclidinyl system was synthesised and evaluated for binding to 5-HT3, 5-HT4 and D2 receptors. In general, the isoquinuclidine derivatives at the 5-position have shown to be more potent as 5-HT3 ligands but they also possess 5-HT4 and D2 properties. However, the results show that the derivatives at the 6-position afforded the most promising compounds in terms of both receptor affinity and selectivity.

Amino-substituted bridged azabicyclic quinolone carboxylic acids and esters

-

, (2008/06/13)

Compounds of the formula STR1 wherein R1 is hydrogen, C1 -C6 alkyl, or a pharmaceutically acceptable cation; Y is cyclopropyl, ethyl or p-fluorophenyl, and X is hydrogen or fluoro, or X and Y taken together form a group ST

Amino-substituted bridged azabicyclic quinolone carboxylic acids and esters

-

, (2008/06/13)

Compounds of the formula wherein R1 is hydrogen, C1-C6 alkyl, or a pharmaceutically acceptable cation;, Y is cyclopropyl, ethyl or p-fluorophenyl, and X is hydrogen or fluoro, or X and Y taken together form a group wherein R3 is hydr

Regioselective Synthesis of Isoquinuclidin-6-ones. Synthesis of an Ibogamine Intermediate

Krow, Grant R.,Shaw, Donald A.,Lynch, Barton,Lester, Walden,Szczepanski, Steven W.,Raghavachari, Ramesh

, p. 2258 - 2262 (2007/10/02)

Addition of benzeneselenenyl chloride to 5,6-dehydroisoquinuclidines 8 followed by dehydrohalogenation and hydrolysis of the derived vinyl selenides 11 affords isoquinuclidin-6-ones 7 regioselectively.The method has been applied to the synthesis of 7-syn-ethylisoquinuclidin-6-one 16, an intermediate in the synthesis of ibogamine 2a.

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