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+ |
Structure of 3456-75-5
*Storage: {[sel_prStorage]}
*Shipping: {[sel_prShipping]}
The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
4.5
*For Research Use Only !
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Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
CAS No. : | 3456-75-5 |
Formula : | C8H5FN2O2 |
M.W : | 180.14 |
SMILES Code : | N#CCC1=CC(F)=CC=C1[N+]([O-])=O |
MDL No. : | MFCD00039742 |
InChI Key : | YETOJTGGLXHUCS-UHFFFAOYSA-N |
Pubchem ID : | 18945 |
GHS Pictogram: |
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Signal Word: | Danger |
Hazard Statements: | H302-H312-H315-H319-H331-H335 |
Precautionary Statements: | P261-P280-P305+P351+P338-P304+P340-P405-P501 |
Class: | 6.1 |
UN#: | 2811 |
Packing Group: | Ⅲ |
* 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.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
32% | With potassium tert-butylate; In tetrahydrofuran; at -20 - -10℃; for 0.333333h; | To a cooled solution of potassium tert-butoxide (3.2 g, 28.4 mmol) in THF (20 ml), a solution of 2-chloroacetonitrile (compound 14b, 1.0 g, 14.2 mmol) and 1-fluoro-4-nitrobenzene (compound 17a, 2.0 g, 14.2 mmol) in THF (20 ml) was added within 10 mins. During the addition the reaction temperature was kept at -10 0C to -200C. About 10 mins after the addition was completed, the mixture was acidified with HCl (1 N) to pH around 5, and extracted with DCM (100 mL) twice. The combined organic layer was washed with water and brine, dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by silica gel column chromatography (eluted with PE:EtOAc = 20 : 1 to 4 : 1) to afford compound 17b (820 mg, 32% yield) 79 [(M-H)-], measured 179 [(M-H)-]. |
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