Home Cart 0 Sign in  

[ CAS No. 18706-26-8 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 18706-26-8
Chemical Structure| 18706-26-8
Structure of 18706-26-8 * Storage: {[proInfo.prStorage]}
Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Quality Control of [ 18706-26-8 ]

Related Doc. of [ 18706-26-8 ]

Alternatived Products of [ 18706-26-8 ]

Product Details of [ 18706-26-8 ]

CAS No. :18706-26-8 MDL No. :MFCD12197299
Formula : C11H5F3N2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 222.17 Pubchem ID :-
Synonyms :

Safety of [ 18706-26-8 ]

Signal Word: Class:
Precautionary Statements: UN#:
Hazard Statements: Packing Group:

Application In Synthesis of [ 18706-26-8 ]

* 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 [ 18706-26-8 ]

[ 18706-26-8 ] Synthesis Path-Downstream   1~2

  • 1
  • copper(l) cyanide [ No CAS ]
  • [ 18706-25-7 ]
  • [ 18706-26-8 ]
YieldReaction ConditionsOperation in experiment
21 g With potassium carbonate In N,N-dimethyl-formamide Reflux; 1.2 (2) Synthesis of 2-(trifluoromethyl)-4-cyanoquinoline 28 g of 4-bromo-2-(trifluoromethyl)quinoline was added to 280 ml of N,N-dimethylformamide.Add 16g of anhydrous potassium carbonate, and then add 21g of cuprous cyanide.Heated to reflux overnight, cooled to room temperature and concentrated.Add water and dichloromethane, extract the liquid, collect the organic phase, and separate the liquid.Dry, concentrated,The residue was separated on a silica gel column to give 21 g of 2-(trifluoromethyl)-4-cyanoquinoline.
  • 2
  • [ 1701-18-4 ]
  • [ 18706-26-8 ]
Same Skeleton Products
Historical Records