Home Cart Sign in  
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| 160658-68-4 Chemical Structure| 160658-68-4

Structure of 160658-68-4

Chemical Structure| 160658-68-4

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

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

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 160658-68-4 ]

CAS No. :160658-68-4
Formula : C7H5Cl2F
M.W : 179.02
SMILES Code : FC1=CC(CCl)=CC=C1Cl
MDL No. :MFCD05864316

Safety of [ 160658-68-4 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P321-P363-P405-P501
Class:8
UN#:3265
Packing Group:

Application In Synthesis of [ 160658-68-4 ]

* 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 [ 160658-68-4 ]

[ 160658-68-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 160658-68-4 ]
  • [ 436-77-1 ]
  • C44H44ClFN2O6 [ No CAS ]
YieldReaction ConditionsOperation in experiment
24% To dimethylsulfoxide (2 mL) was added fangehinoline (80 mg, 0.13 mmol), followed by the addition of potassium tert-butoxide (22.5 mg, 0.1971 mmol) at 00 C. The reaction solution was warmed to room temperature and stirred for 0.5 br. 3-fluoro-4-ehloro benzyl chloride (26.5 mg, 0.12 mmol) dissolyed in dimethylsulfoxide was added dropwise to the reaction solution. The reaction solution was heated up to 40 C. and stirred for 2 br. After the reaction was eompleted, water (20 mL) was added to the reaetion solution and diebloromethane (5 mLx3) was used for extraetion. The organie phases were eombined, washed with saturated salt solution and rotayapped. The resulted erude produet was separated and purifed tbrough preparatiye thin layer ebromatography (diebloromethane: methanol 10:1) to giye the bright yellow powdery eompound BS-EC-206 (23.6 mg, yield 24%). LC-MS: retentiontime: 1 .l0min (99.12%); mlz 751 [M÷H], 376 [?2M+H]. ?H NMR (301 MHz, partial assignment of signals in CDC13) 6 2.55 (s, 3H, N-CH3), 3.48 (s, 3H, 6?-OCH3), 3.76 (s, 3H, 6-OCH3), 3.94 (s, 3H, 12-OCH3),5.81 (s, 1H, 8?-H), 6.60 (s, 1H, H-benzene ring), 6.74 (m, 1H, H-benzene ring).
24% Example 2: The synthesis of compound BS-FC-206 [0100] To dimethylsulfoxide (2 mL) was added <strong>[436-77-1]fangchinoline</strong> (80 mg, 0.13 mmol), followed by the addition of potassium tert-butoxide (22.5 mg, 0.1971 mmol) at 0 C. The reaction solution was warmed to room temperature and stirred for 0.5 hr. 3-fluoro-4-chloro benzyl chloride (26.5 mg, 0.12 mmol) dissolved in dimethylsulfoxide was added dropwise to the reaction solution. The reaction solution was heated up to 40 C and stirred for 2 hr. After the reaction was completed, water (20mL) was added to the reaction solution and dichloromethane (5 mL×3) was used for extraction. The organic phases were combined, washed with saturated salt solution and rotavapped. The resulted crude product was separated and purifed through preparative thin layer chromatography (dichloromethane: methanol=10:1) to give the bright yellow powdery compound BS-FC-206 (23.6mg, yield 24%). LC-MS: retention time: 1.10 min (99.12%); m/z 751 [M+H]+, 376 [1/2M+H]+. 1H NMR (301 MHz, partial assignment of signals in CDCl3) delta 2.55(s, 3H, N-CH3), 3.48(s, 3H, 6'-OCH3), 3.76(s, 3H, 6-OCH3), 3.94(s, 3H, 12-OCH3), 5.81(s, 1H, 8'-H), 6.60(s, 1H, H- benzene ring), 6.74 (m, 1H, H- benzene ring).
 

Historical Records

Technical Information

Categories