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| 1246617-44-6 Chemical Structure| 1246617-44-6

Structure of 1246617-44-6

Chemical Structure| 1246617-44-6

*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 [ 1246617-44-6 ]

CAS No. :1246617-44-6
Formula : C14H15N3O3
M.W : 273.29
SMILES Code : O=C(C1=C(OCC2=CC=CC=C2)C(C=CN1N)=O)NC
MDL No. :N/A

Safety of [ 1246617-44-6 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P301+P330+P331-P303+P361+P353-P363-P304+P340-P310-P321-P260-P264-P280-P305+P351+P338-P405-P501
Class:8
UN#:3263
Packing Group:

Application In Synthesis of [ 1246617-44-6 ]

* 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 [ 1246617-44-6 ]

[ 1246617-44-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 22929-52-8 ]
  • [ 1246617-44-6 ]
  • C18H19N3O4 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With acetic acid; In tetrahydrofuran; at 90℃; for 3h;Microwave irradiation; To a solution of l-amino-3-(benzyloxy)-N-methyl-4-oxo-l,4-dihydropyridine-2- carboxamide (300 mg, 1.098 mmol) in tetrahydrofuran (6 mL) and acetic acid (0.3 mL) was added <strong>[22929-52-8]dihydrofuran-3(2H)-one</strong> (189 mg, 2.195 mmol) and the mixture was heated by microwave irradiation at 90 C for 3 hours, cooled to room temperature, quenched with water (1 mL) and diluted with dichloromethane (10 mL). The organic layer was dried over anhydrous sodium sulfate, filtered and the filtrate was concentrated. The crude residue was purified using column chromatography to give intermediate compound 25a. XH NMR (400 MHz, CDC13) delta 7.31-7.35 (m, 5H), 7.03-7.06 (m, 1H), 6.45-6.47 (m, 1H), 6.31 (bs, 1H), 5.23 (s, 2H), 4.32-4.41 (m, 2H),4.05-4.12 (m, 2H), 2.86-2.89 (m, 1H), 2.71-2.74 (m, 4H).
With acetic acid; In 1,4-dioxane; at 20℃; for 24h; Step D - Synthesis of Compound Id A solution of Compound lc (1000 mg, 3.66 mmol) in dioxane (5.0 mL) was treated at room temperature with 3-oxotetrahydrofuran (1260 mg, 14.64 mmol) and AcOH (0.050 mL). The reaction mixture was capped and stirred at room temperature for 24 hours. The reaction mixture was directly applied to a dry 80g silica gel column. Gradient elution with 0 to 30% MeOH/ dichloromethane provided the intermediate that was taken up in DMSO (6 mL) and treated with diethyl 2-bromoethylphosphonate (1.330 ml, 7.32 mmol), tetrabutylammonium hydroxide triacontahydrate (585 mg, 0.732 mmol) and potassium hydroxide (616 mg, 10.98 mmol). The reaction mixture was allowed to stir at room temperature for 4 hours, neutralized with glacial acetic acid and directly purified using RP-MPLC to provide Compound Id which was used without further purification. Mass Calc'd for C24H32N3O7P: 505.1, found 506.1 (M+H)+;
 

Historical Records