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| 40327-96-6 Chemical Structure| 40327-96-6

Structure of 40327-96-6

Chemical Structure| 40327-96-6

*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 [ 40327-96-6 ]

CAS No. :40327-96-6
Formula : C10H22N2
M.W : 170.30
SMILES Code : NC1CC(C)(C)N(C)C(C)(C)C1
MDL No. :MFCD01861832

Safety of [ 40327-96-6 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301
Precautionary Statements:P264-P270-P301+P310-P321-P330-P405-P501
Class:6.1
UN#:2810
Packing Group:

Application In Synthesis of [ 40327-96-6 ]

* 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 [ 40327-96-6 ]

[ 40327-96-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 298709-29-2 ]
  • [ 40327-96-6 ]
  • [ 1190424-32-8 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In dimethyl sulfoxide; at 115℃; for 1h;microwave irradiation; Example 122Synthesis of 3-[1,2,2,6,6-pentamethylpiperidin-4-yl)amino]-5-[4-(quinolin-3-yl)-9H-carbazol-9-yl]pyridin-2-carboxamideStage 1:682 mg of <strong>[298709-29-2]2-cyano-3,5-difluoropyridine</strong>, 995 mg of 4-amino-1,2,2,6,6-pentamethylpiperidine and 1.346 mg of potassium carbonate in 10 ml of dimethyl sulphoxide are introduced into a 20 ml microwave tube reactor.The mixture is then heated in the microwave for 1 hour at 115° C.The reaction medium is run into 100 ml of water and 100 ml of ethyl acetate.The aqueous phase is re-extracted twice with 50 ml of ethyl acetate.The combined organic phases are washed with water and then with a saturated aqueous solution of sodium chloride, dried over sodium sulphate and concentrated under reduced pressure.After purification by flash chromatography on 70 g of silica gel, elution being carried out with a mixture of dichloromethane, methanol and 4N aqueous ammonia (99/1/0.8 by volume), and the first eluted product being recovered, 290 mg of 2-cyano-5-fluoro-3-(1,2,2,6,6-pentamethylpiperidin-4-yl)aminopyridine are thus obtained in the form of an ecru powder, the characteristics of which are the following:1H NMR spectrum (400 MHz, DMSO-d6) delta ppm 1.07 (s, 6 H) 1.08 (s, 6 H) 1.46 (t, J=12.1 Hz, 2 H) 1.73 (dd, J=12.5, 3.5 Hz, 2 H) 2.18 (s, 3 H) 3.70-3.82 (m, 1 H) 6.27 (d, J=8.6 Hz, 1 H) 7.18 (dd, J=11.8, 2.4 Hz, 1 H) 7.89 (d, J=2.4 Hz, 1 H).
With potassium carbonate; In dimethyl sulfoxide; at 115℃; for 1h;Inert atmosphere; Microwave irradiation; 682 mg of <strong>[298709-29-2]2-cyano-3,5-difluoropyridine</strong>, 995 mg of 4-amino-1,2,2,6,6-pentamethylpiperidine and 1.346 g of potassium carbonate in 10 ml of dimethyl sulphoxide are charged to a 20 ml microwave tube-reactor.The mixture is then microwave-heated for 1 hour at 115° C.The reaction medium is run into 100 ml of water and 100 ml of ethyl acetate.The aqueous phase is re-extracted twice with 50 ml of ethyl acetate.The combined organic phases are washed with water and then with a saturated aqueous solution of sodium chloride, dried over sodium sulphate and concentrated under reduced pressure.After flash chromatography on silica gel (15-40 mum), elution being carried out with a mixture of dichloromethane, methanol and 4N aqueous ammonia (99:1:0.8 v/v/v), with the first eluted product being collected, 290 mg of 2-cyano-5-fluoro-3-(1,2,2,6,6-pentamethylpiperidin-4-ylamino)pyridine are obtained in the form of an ecru powder, the characteristics of which are the following:1H NMR spectrum (400 MHz, delta in ppm, DMSO-d6): 1.07 (s, 6H); 1.08 (s, 6H); 1.46 (t, J=12.1 Hz, 2H); 1.73 (dd, J=12.5 and 3.5 Hz, 2H); 2.18 (s, 3H); 3.70 to 3.82 (m, 1H); 627 (d, J=8.6 Hz, 1H); 7.18 (dd, J=11.8 and 2.4 Hz, 1H); 7.89 (d, J=2.4 Hz, 1H)
  • 2
  • [ 207399-07-3 ]
  • [ 40327-96-6 ]
  • C46H65N4(1+)*I(1-) [ No CAS ]
YieldReaction ConditionsOperation in experiment
77.5% In N,N-dimethyl-formamide; at 100℃; for 2h;Inert atmosphere; Starting material C4 (1.32 g, 2 mmol), pentamethylpiperidine (0.34 g, 2 mmol)And 15mL DMF was added to a 50mL round bottom flask,Vacuuming and replacing N2 three times,The temperature was raised to 100 C for 2 hours. After cooling the reaction solution to room temperature,Concentrate the reaction solution in vacuo,Purified by silica gel column chromatography to give 1.24gBlue-black solid powder,The yield was 77.50%.
 

Historical Records