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. : | 51984-46-4 | MDL No. : | MFCD08234494 |
Formula : | C7H9NO2 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | RDXXAIGOEPIQPK-UHFFFAOYSA-N |
M.W : | 139.15 | Pubchem ID : | 5324774 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P280-P305+P351+P338 | UN#: | |
Hazard Statements: | H302 | 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 |
---|---|---|
7% | With potassium hydroxide; In water; dimethyl sulfoxide; | a 3-Methoxy(2-hydroxymethyl)pyridine To a mixture of ground potassium hydroxide (10.2 g, 0.186 mol) in dimethylsulphoxide (15 ml) under nitrogen was added 3-hydroxy(2-hydroxymethyl)pyridine hydrochloride (5.0 g, 0.031 mol) in dimethylsulphoxide (15 ml) over 0.25 h. The reaction was stirred at room temperature for 1 h before the addition of methyl iodide (1.92 ml, 0.0309 mol) and then stirred at room temperature overnight. Water (100 ml) was added and the solution acidified to pH 1 with 2N hydrochloric acid, washed with dichloromethane (*3) and then basified with solid potassium carbonate until pH 12 was attained. The aqueous was extracted with dichloromethane (*3), dried (MgSO4), evaporated in vacuo and the residue purified by chromatography on silica gel, eluding with dichloromethane/methanol/ammonia (90:5:0.5), to give the title-compound (300 mg, 7%). 1H NMR (360 MHz, CDCl3) δ 3.85 (3H, s, CH3), 4.74 (2H, s, CH2), 7.12 (1H, d, J=8.3 Hz, Ar-H), 7.21 (1H, m, Ar-H), 8.15 (1H, d, J=4.8 Hz, Ar-H). |
[ 1588441-00-2 ]
(3-Methoxypyridin-2-yl)methanamine hydrochloride
Similarity: 0.82
[ 16665-38-6 ]
(4-Methoxypyridin-2-yl)methanol
Similarity: 0.80
[ 16665-38-6 ]
(4-Methoxypyridin-2-yl)methanol
Similarity: 0.80
[ 1122-43-6 ]
2,6-Dimethyl-3-hydroxypyridine
Similarity: 0.76
[ 1588441-00-2 ]
(3-Methoxypyridin-2-yl)methanamine hydrochloride
Similarity: 0.82