Purity | Size | Price | VIP Price | USA Stock *0-1 Day | Global Stock *5-7 Days | Quantity | ||||||
{[ item.p_purity ]} | {[ item.pr_size ]} | Inquiry |
{[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price) ]} {[ getRatePrice(item.pr_usd,item.pr_rate,1,item.pr_is_large_size_no_price) ]} |
{[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price) ]} | Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price) ]} {[ getRatePrice(item.pr_usd,1,item.mem_rate,item.pr_is_large_size_no_price) ]} | {[ item.pr_usastock ]} | in stock Inquiry - | {[ item.pr_chinastock ]} | {[ item.pr_remark ]} in stock Inquiry - | Login | Inquiry |
Please Login or Create an Account to: See VIP prices and availability
CAS No. : | 4837-19-8 | MDL No. : | MFCD00236224 |
Formula : | C8H6F2O3 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | OKKDGIXOKWOMRD-UHFFFAOYSA-N |
M.W : | 188.13 | Pubchem ID : | 842614 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H315-H319-H335 | Packing Group: | |
GHS Pictogram: |
* 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 |
---|---|---|
83% | To a solution of 3-(difluoromethoxy)benzoic acid (2.82 g, 15 mmol) in DCM (30 mL) was added Et3N (3.34 g, 33 mmol) followed by EDC (3.43 g, 18 mmol) and HOBt (0.27 g, 2 mmol) at room temperature. The reaction mixture was stirred at room temperature for 30 min. Then 0-(tert-butyl)-L- serine methyl ester hydrochloride (3.17 g, 15 mmol) was added and reaction mixture was stirred at room temperature for 12h. Evaporation of solvent under vacuum gave crude residue which was treated with saturated aqueous NaHC03 solution (10 mL), then extracted with ethyl acetate (2 x 100 mL). Dried (Na2S04), filtered and evaporation of solvent under vacuum gave almost pure product as pale yellow syrup which was used as such in the next. Yield : 4.33 g (83percent), LCMS m/z: 346.32 (M+H)+. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With tris(2,2-bipyridine)ruthenium(II) hexafluorophosphate; In acetonitrile; at 23℃; for 12h;Irradiation; Glovebox; Sealed tube; Inert atmosphere; | General procedure: In a glovebox, to an oven-dried 20 mL screw cap vial was added 1- (difluoromethoxy) -3-methyl-6-nitro-4- (trifluoromethyl) -lff- benzo [d] [1, 2, 3] triazol-3-ium trifluoromethanesulfonate (la) (92.4 mg, 0.200 mmol, 1.00 equiv), (hetero) arene (2.00 mmol, 10.0 equiv), Ru (bpy) 3 (PF6) 2, (0.860 mg, 1.00 pmol, 0.500 mol%), and MeCM (1.00 mL, 0.200 M, with respect to la) . To this suspension or solution was added a magnetic stir bar. Next, the reaction vial was capped and taken out of the glovebox. The reaction mixture was stirred at ambient temperature (23 C) and irradiated with blue LEDs (30 W, Xmax = 450 nm) which was placed 20.0 m from the vial for 12 h. To determine the yield of the products, an internal standard, trifluorotoluene (PhCF3) (14.6 mg, 12.3 pL, 0.100 mmol, 0.500 equiv) was added to the vial. Then, a 100 pL of the reaction mixture was taken and then dilute with 500 pL CD3CN followed by 19F NMR (the NMR sample was recombined with the rest of the reaction mixture afterward) . The combined reaction mixture was then purified by HPLC on the Luna PFP(2) preparative column (250 x 21.2 mm) column eluting with MeCN:H20 (v/v) with a flow rate of 10.6 mL/min to provide the purified products. In cases of closely-eluting peaks, products were isolated as a mixture of isomers. Afterwards, the products were extracted with CDC13 (3 x 1 mL) , dried with magnesium sulfate, and filtered. The filtrate was concentrated in vacuo to afford the desired product (s). For very volatile compounds, the products were extracted immediately with CDCI3 (l x l mL) and then directly characterized. 1H and 13C NMR of these Compound (s) contains MeCN residue signal (1H NMR: □ 1.94, 13C NMR: u 118.26, 1.32 in CDCI3 ) |
[ 4837-20-1 ]
4-(Difluoromethoxy)benzoic acid
Similarity: 0.98
[ 1014-81-9 ]
3-(Trifluoromethoxy)benzoic acid
Similarity: 0.96
[ 330-12-1 ]
4-(Trifluoromethoxy)benzoic acid
Similarity: 0.94
[ 148438-00-0 ]
Methyl 3-(trifluoromethoxy)benzoate
Similarity: 0.91
[ 175278-21-4 ]
2-(Trifluoromethoxy)terephthalic acid
Similarity: 0.90
[ 4837-20-1 ]
4-(Difluoromethoxy)benzoic acid
Similarity: 0.98
[ 1014-81-9 ]
3-(Trifluoromethoxy)benzoic acid
Similarity: 0.96
[ 330-12-1 ]
4-(Trifluoromethoxy)benzoic acid
Similarity: 0.94
[ 148438-00-0 ]
Methyl 3-(trifluoromethoxy)benzoate
Similarity: 0.91
[ 175278-21-4 ]
2-(Trifluoromethoxy)terephthalic acid
Similarity: 0.90
[ 4837-20-1 ]
4-(Difluoromethoxy)benzoic acid
Similarity: 0.98
[ 1014-81-9 ]
3-(Trifluoromethoxy)benzoic acid
Similarity: 0.96
[ 330-12-1 ]
4-(Trifluoromethoxy)benzoic acid
Similarity: 0.94
[ 148438-00-0 ]
Methyl 3-(trifluoromethoxy)benzoate
Similarity: 0.91
[ 175278-21-4 ]
2-(Trifluoromethoxy)terephthalic acid
Similarity: 0.90
[ 4837-20-1 ]
4-(Difluoromethoxy)benzoic acid
Similarity: 0.98
[ 1014-81-9 ]
3-(Trifluoromethoxy)benzoic acid
Similarity: 0.96
[ 330-12-1 ]
4-(Trifluoromethoxy)benzoic acid
Similarity: 0.94
[ 175278-21-4 ]
2-(Trifluoromethoxy)terephthalic acid
Similarity: 0.90
[ 1979-29-9 ]
2-(Trifluoromethoxy)benzoic acid
Similarity: 0.88
[ 4837-20-1 ]
4-(Difluoromethoxy)benzoic acid
Similarity: 0.98
[ 85684-61-3 ]
3-(Difluoromethoxy)benzaldehyde
Similarity: 0.88
[ 162401-62-9 ]
3-(Cyclopropylmethoxy)-4-(difluoromethoxy)benzoic acid
Similarity: 0.87
[ 73960-07-3 ]
4-(Difluoromethoxy)benzaldehyde
Similarity: 0.87
[ 127842-54-0 ]
3,4-Bis(difluoromethoxy)benzaldehyde
Similarity: 0.85