4-cyanobicyclo[2.2.2]octane-1-carboxylic Acid

Base Information

• Chemical Name: 4-cyanobicyclo[2.2.2]octane-1-carboxylic Acid
• CAS No.: 15941-09-0
• Molecular Formula: C10H13NO2
• Molecular Weight: 179.219
• Hs Code.: 2922498590
• European Community (EC) Number: 871-785-2
• DSSTox Substance ID: DTXSID00394037
• Nikkaji Number: J1.729.662K
• Wikidata: Q82193187
• Mol file: 15941-09-0.mol

Synonyms:4-cyanobicyclo[2.2.2]octane-1-carboxylic Acid;15941-09-0;Bicyclo[2.2.2]octane-1-carboxylic acid, 4-cyano-;SCHEMBL7396289;DTXSID00394037;ONXKUOTWYIGFMY-UHFFFAOYSA-N;MFCD00967723;BS-42798;1-carboxy-4-cyano-bicyclo[2.2.2]-octane;CS-0092251;4-cyanobicyclo[2.2.2]octane-1-carboxylicAcid;D75331;EN300-149355

Chemical Property of 4-cyanobicyclo[2.2.2]octane-1-carboxylic Acid

Chemical Property:

• Boiling Point: 359.8±42.0 °C(Predicted)
• PSA: 61.09000
• Density: 1.22±0.1 g/cm3(Predicted)
• LogP: 1.93518
• XLogP3: 0.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 179.094628657
• Heavy Atom Count: 13
• Complexity: 275

Purity/Quality:

97% ^*data from raw suppliers

4-Cyanobicyclo[2.2.2]octane-1-carboxylic acid ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CC2(CCC1(CC2)C#N)C(=O)O

Technology Process of 4-cyanobicyclo[2.2.2]octane-1-carboxylic Acid

There total 6 articles about 4-cyanobicyclo[2.2.2]octane-1-carboxylic Acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

4-(ethoxycarbonyl)bicyclo[2.2.2]octane-1-carboxylic acid (834-50-4) → 4-cyanobicyclo<2.2.2>octane-1-carboxylic acid (15941-09-0)

Guidance literature:

Multi-step reaction with 3 steps

1: triethylamine; chlorocarbonic acid ethyl ester; NH₃

2: POCl₃; 1,2-dichloro-ethane

3: ethanolic KOH

With potassium hydroxide; ammonia; chloroformic acid ethyl ester; 1,2-dichloro-ethane; triethylamine; trichlorophosphate;

DOI:10.3758/BF03211828

Reference yield:

4-cyano-bicyclo[2.2.2]octane-1-carboxylic acid ethyl ester (54829-94-6) → 4-cyanobicyclo<2.2.2>octane-1-carboxylic acid (15941-09-0)

Guidance literature:

With potassium hydroxide;

DOI:10.3758/BF03211828

Reference yield:

Bicyclo<2.2.2.>octan-1,4-dicarbonsauere-ethylester (1659-75-2) → 4-cyanobicyclo<2.2.2>octane-1-carboxylic acid (15941-09-0)

Guidance literature:

Multi-step reaction with 4 steps

1: ethanolic KOH

2: triethylamine; chlorocarbonic acid ethyl ester; NH₃

3: POCl₃; 1,2-dichloro-ethane

4: ethanolic KOH

With potassium hydroxide; ammonia; chloroformic acid ethyl ester; 1,2-dichloro-ethane; triethylamine; trichlorophosphate;

DOI:10.3758/BF03211828

upstream raw materials:

4-cyano-bicyclo[2.2.2]octane-1-carboxylic acid ethyl ester

1-cyano-4-phenylbicyclo<2.2.2>octane

4-(ethoxycarbonyl)bicyclo[2.2.2]octane-1-carboxylic acid

Bicyclo<2.2.2.>octan-1,4-dicarbonsauere-ethylester