No renderable structure data available
C1CCC(C1)NC2=C(C=CC(=C2)Cl)C#NChemical Intermediate
Structures, identifiers and computed properties have been matched to the database record by CAS.
| Intermediates | 4-chloro-2-(cyclopentylamino)benzonitrile |
|---|---|
| IUPAC Name | — |
| CAS Number | 939812-57-4 |
| Database ID | 43681510 |
| Molecular Formula | — |
| Molecular Weight | — |
Product Information
4-chloro-2-(cyclopentylamino)benzonitrile (CAS 939812-57-4) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
Potential Applications
For professional research and industrial use only
Database ID 43681510
Safety Notice
For professional research and industrial use only. Review the supplier safety data sheet before handling.
Synthesis data
11 reactions · 11 references
Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-657cb1bf1d73438f99d586292649f26fConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-f6ad81dfc3414dfeb0fba5bb0fa7edecConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: 4-Chloro-2-(cyclopentylamino)benzonitrile and concentrated sulfuric acid were added to water, followed by stirring while heating under reflux. The reaction liquid was neutralized by adding sodium hydroxide to the reaction liquid, and the organic layer was extracted with chloroform to obtain 4-chloro-2-(cyclopentylamino)benzoic acid. while heating under reflux The reaction liquid to the reaction liquid the organic layer was extracted with chloroform
Source ID: ord-fcc97365de3b4e75b2a6fce892542172Conditions: temp:100.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Cyclopentylamine and potassium carbonate were added to a DMF solution of 4-chloro-2-fluorobenzonitrile, followed by stirring at 100° C. for 12 hours. By post-treating the reaction liquid, 4-chloro-2-(cyclopentylamino)benzonitrile was obtained. By post-treating the reaction liquid
Source ID: ord-5f11b7f2f9c34c1c822d468a41e92ad5Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: 4-Chloro-2-(cyclopentylamino)benzonitrile and concentrated sulfuric acid were added to water, followed by stirring while heating under reflux. The reaction liquid was neutralized by adding sodium hydroxide to the reaction liquid, and the organic layer was extracted with chloroform to obtain 4-chloro-2-(cyclopentylamino)benzoic acid. while heating under reflux The reaction liquid to the reaction liquid the organic layer was extracted with chloroform
Source ID: ord-fcc97365de3b4e75b2a6fce892542172Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: 4-Chloro-2-(cyclopentylamino)benzonitrile and concentrated sulfuric acid were added to water, followed by stirring while heating under reflux. The reaction liquid was neutralized by adding sodium hydroxide to the reaction liquid, and the organic layer was extracted with chloroform to obtain 4-chloro-2-(cyclopentylamino)benzoic acid. while heating under reflux The reaction liquid to the reaction liquid the organic layer was extracted with chloroform
Source ID: ord-fcc97365de3b4e75b2a6fce892542172Conditions: temp:100.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Cyclopentylamine and potassium carbonate were added to a DMF solution of 4-chloro-2-fluorobenzonitrile, followed by stirring at 100° C. for 12 hours. By post-treating the reaction liquid, 4-chloro-2-(cyclopentylamino)benzonitrile was obtained. By post-treating the reaction liquid
Source ID: ord-5f11b7f2f9c34c1c822d468a41e92ad5Conditions: temp:100.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Cyclopentylamine and potassium carbonate were added to a DMF solution of 4-chloro-2-fluorobenzonitrile, followed by stirring at 100° C. for 12 hours. By post-treating the reaction liquid, 4-chloro-2-(cyclopentylamino)benzonitrile was obtained. By post-treating the reaction liquid
Source ID: ord-5f11b7f2f9c34c1c822d468a41e92ad5Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-f6ad81dfc3414dfeb0fba5bb0fa7edecConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: 4-Chloro-2-(cyclopentylamino)benzonitrile and concentrated sulfuric acid were added to water, followed by stirring while heating under reflux. The reaction liquid was neutralized by adding sodium hydroxide to the reaction liquid, and the organic layer was extracted with chloroform to obtain 4-chloro-2-(cyclopentylamino)benzoic acid. while heating under reflux The reaction liquid to the reaction liquid the organic layer was extracted with chloroform
Source ID: ord-fcc97365de3b4e75b2a6fce892542172Conditions: temp:100.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Cyclopentylamine and potassium carbonate were added to a DMF solution of 4-chloro-2-fluorobenzonitrile, followed by stirring at 100° C. for 12 hours. By post-treating the reaction liquid, 4-chloro-2-(cyclopentylamino)benzonitrile was obtained. By post-treating the reaction liquid
Source ID: ord-5f11b7f2f9c34c1c822d468a41e92ad5PubChem References
These sources are listed in the compound's public database record.
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