成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

Home Cart 0 Sign in  

[ CAS No. 10386-84-2 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 10386-84-2
Chemical Structure| 10386-84-2
Structure of 10386-84-2 * Storage: {[proInfo.prStorage]}

Please Login or Create an Account to: See VIP prices and availability

Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Search after Editing

* Storage: {[proInfo.prStorage]}

* Shipping: {[proInfo.prShipping]}

Quality Control of [ 10386-84-2 ]

Related Doc. of [ 10386-84-2 ]

Alternatived Products of [ 10386-84-2 ]
Product Citations

Product Details of [ 10386-84-2 ]

CAS No. :10386-84-2 MDL No. :MFCD00000310
Formula : C12Br2F8 Boiling Point : -
Linear Structure Formula :- InChI Key :YXLMNFVUNLCJJY-UHFFFAOYSA-N
M.W : 455.92 Pubchem ID :82600
Synonyms :

Safety of [ 10386-84-2 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 10386-84-2 ]

* 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 [ 10386-84-2 ]

[ 10386-84-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 10386-84-2 ]
  • [ 15424-38-1 ]
  • 4-bromo-4'-[N-(9-anthracenyl)-N-phenylamino]-2,2',3,3',5,5',6,6'-octafluoro-1,1'-biphenyl [ No CAS ]
YieldReaction ConditionsOperation in experiment
In a nitrogen flow, 160 mg (0.282 mmol) of palladium bis (benzylideneacetone) and 170 mg (0.846 mmol) of tri-tert-butylphosphine were dissolved in 40 ml of toluene and then stirred for 15 minutes at room temperature. Then, 0.58 g (1.27 mmol) of 4,4'- [ F] [DIBROMO-2, 2',] 3, [3',] 5, 5', 6, [6'-OCTAFLUORO-1,] 1'-biphenyl dissolved in 50 ml of toluene was dropped into the mixture and it was stirred for 30 minutes. Furthermore, 0.34 g (1.27 mmol) of [N- (9-ANTHRACENYL)-] N-phenylamine was dissolved in 50 ml of toluene and was then dropped therein, followed by the addition of 0.18 g (1.91 mmol) of sodium tert-butoxide. Then, the mixture was heated and stirred for about 8 hours in an oil bath heated at [120C.] After returning the reaction solution to room temperature, 50 ml of water was added thereto and the resultant solution was then separated into an aqueous layer and an organic layer. Furthermore, the aqueous layer was extracted with toluene and ethyl acetate, and was then combined with the previous organic layer and dried with magnesium sulfate. The solvent was evaporated and then the residue was purified by silicagel-column chromatography (toluene : hexane = [1 :] 2) to obtain 0.55 g of [4-BROMO-4'-[N-(9-ANTHRACENYL)-N-] [PHENYLAMINO]-2,] 2', 3, 3', 5, 5', 6, [6'-OCTAFLUORO-1,] 1'- biphenyl.
Recommend Products
Same Skeleton Products

Technical Information

Historical Records
; ;