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. 12093-10-6 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
HazMat Fee +

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 12093-10-6
Chemical Structure| 12093-10-6
Structure of 12093-10-6 * 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 [ 12093-10-6 ]

Related Doc. of [ 12093-10-6 ]

Alternatived Products of [ 12093-10-6 ]
Product Citations

Product Details of [ 12093-10-6 ]

CAS No. :12093-10-6 MDL No. :MFCD00001429
Formula : C11H10FeO Boiling Point : No data available
Linear Structure Formula :(C5H5)Fe(C5H4C(O)H) InChI Key :-
M.W : 214.04 Pubchem ID :-
Synonyms :

Safety of [ 12093-10-6 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P264-P270-P301+P310-P330-P405-P501 UN#:3467
Hazard Statements:H301 Packing Group:Ⅱ
GHS Pictogram:

Application In Synthesis of [ 12093-10-6 ]

* 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 [ 12093-10-6 ]

[ 12093-10-6 ] Synthesis Path-Downstream   1~12

  • 1
  • [ 12093-10-6 ]
  • [ 498-63-5 ]
  • C10H9FeCHNC4H7CH2O [ No CAS ]
  • C10H9FeCHNC4H7CH2O [ No CAS ]
  • 2
  • [ 12093-10-6 ]
  • [ 498-63-5 ]
  • C10H9FeCHNC4H7CH2O [ No CAS ]
  • 3
  • [ 12093-10-6 ]
  • [ 24629-25-2 ]
  • (2S,3S)-2-[(ferrocenylidene)-amino]-3-methyl-pentan-1-ol [ No CAS ]
  • 4
  • [ 1293-65-8 ]
  • [ 112939-59-0 ]
  • [ 12093-10-6 ]
  • 1,1''-biferrocene [ No CAS ]
  • [ 864370-86-5 ]
  • [ 864371-01-7 ]
  • 5
  • [ 12093-10-6 ]
  • [ 784-04-3 ]
  • Anth-Fe [ No CAS ]
  • 6
  • [ 12093-10-6 ]
  • [ 7732-18-5 ]
  • [ 1671-88-1 ]
  • N-4-[3,5-di-(2-pyridyl)-1,2,4-triazoyl]ferrocene carbimine [ No CAS ]
  • 7
  • [ 12093-10-6 ]
  • [ 4506-66-5 ]
  • [ 1204425-72-8 ]
  • 8
  • [ 12093-10-6 ]
  • [ 24629-25-2 ]
  • (2S,3S)-2-[(ferrocenylmethyl)amino]-3-methylpentan-1-ol [ No CAS ]
YieldReaction ConditionsOperation in experiment
85% With sodium tetrahydroborate; potassium carbonate; In chloroform; for 1.5h;Reflux; Inert atmosphere; Schlenk technique; General procedure: Ferrocenecarboxaldehyde (856 mg, 4.0 mmol) and amino alcohol(4.2 mmol) were dissolved in previously dried chloroform(40 mL; dried over K2CO3) and the resulting solution was heated at reflux under argon for 90 min. Then, the solution was cooled to room temperature, the solvent was removed under reduced pressure and the red?brown residue immediately re-dissolved indry methanol (40 mL; distilled from a MeONa solution). The methanol\ic solution was cooled in an ice bath and treated slowly with solid NaBH4 (756 mg, 20 mmol over 30 min). After adding all the NaBH4, the mixture was stirred at 0°C for 1 h and at room temperature for further 90 min. Then, the cooled mixture was quenched with an aqueous solution of NaOH (10percent, 40 mL) and extracted withCH2Cl2 (2 40 mL). The combined organic layer was washed withbrine (2 40 mL), dried over anhydrous MgSO4, and evaporated,leaving the crude product as a yellow?brown solid. Subsequentpurification by column chromatography (silica gel, dichloromethane?methanol 10:1) led to the development of two bands: the first(minor) one containing mostly ferrocenyl methanol, followed by the major band of the amino alcohol. Careful evaporation of the second fraction afforded pure ferrocene based amino alcohol as an amber oil, which slowly solidifies to a brown solid.
  • 9
  • [ 12093-10-6 ]
  • [ 4985-46-0 ]
  • C20H22FeN2O2 [ No CAS ]
  • 10
  • [ 12093-10-6 ]
  • [ 1080-12-2 ]
  • (1E,4E)-1-ferrocenyl-5-(4-hydroxy-3-methoxyphenyl)penta-1,4-dien-3-one [ No CAS ]
  • 11
  • [ 12093-10-6 ]
  • [ 1986-47-6 ]
  • C20H19FeN [ No CAS ]
  • 12
  • [ 12093-10-6 ]
  • [ 525-03-1 ]
  • C24H19FeN [ No CAS ]
Recommend Products
Same Skeleton Products
Historical Records
; ;