Home Cart 0 Sign in  

[ CAS No. 3894-09-5 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 3894-09-5
Chemical Structure| 3894-09-5
Structure of 3894-09-5 * Storage: {[proInfo.prStorage]}
Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Quality Control of [ 3894-09-5 ]

Related Doc. of [ 3894-09-5 ]

Alternatived Products of [ 3894-09-5 ]

Product Details of [ 3894-09-5 ]

CAS No. :3894-09-5 MDL No. :MFCD00001477
Formula : C14H18O2 Boiling Point : -
Linear Structure Formula :- InChI Key :AAJLPPDFIRPBDA-UHFFFAOYSA-N
M.W : 218.29 Pubchem ID :97942
Synonyms :

Safety of [ 3894-09-5 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P233-P260-P261-P264-P271-P280-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501 UN#:N/A
Hazard Statements:H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 3894-09-5 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 3894-09-5 ]

[ 3894-09-5 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 103-82-2 ]
  • [ 953-91-3 ]
  • [ 3894-09-5 ]
YieldReaction ConditionsOperation in experiment
94% Stage #1: phenylacetic acid With lithium diethylamide In tetrahydrofuran at -78℃; for 0.5h; Stage #2: cyclohexyl tosylate In tetrahydrofuran at 20℃; for 4h;
With n-butyllithium In tetrahydrofuran at -70 - -20℃;
  • 2
  • [ 3894-09-5 ]
  • [ 26487-67-2 ]
  • 2-(hexahydro-1H-azepin-1-yl)ethyl cyclohexylphenylethanoate [ No CAS ]
  • 3
  • [ 3894-09-5 ]
  • [ 27841-33-4 ]
  • N-(2-amino-4,5-dimethoxyphenyl)-2-cyclohexyl-2-phenylacetamide [ No CAS ]
  • 5
  • [ 544-13-8 ]
  • [ 3894-09-5 ]
  • [ 1121-89-7 ]
  • [ 3893-23-0 ]
YieldReaction ConditionsOperation in experiment
92% With aluminum (III) chloride at 200℃; for 2.5h; Sealed tube; Thermal-Catalyzed Reaction of Acids 1 with Glutaronitrile; General Procedure 1 (GP1) General procedure: In a glass tube, the glutaronitrile (282 mg, 3.0 mmol, 1.0 equiv) was added to a mixture ofthe respective acid 1(3.0 mmol) and AlCl3(8mg, 0.06 mmol, 0.02 equiv). The tubewas then sealed (with a screwcap) and the mixture was allowed to stir at 200 °C for 5 h. After completion of the reaction, the crude mixture was diluted with EtOH (10 mL), silica gel (3 g) was then added to this crude material to make a solid deposit after evaporation of the EtOH. A silica gelcolumn chromatography (eluent: PE-EtOAc, 95:5) finally afforded the pure nitrile together with the cyclic imide. Conversion into the desired nitrile was determined by 1H NMR analysis of the crude mixture. Given yields were reported for isolated products (Table 2).
Same Skeleton Products
Historical Records