2-hydroxymethyl-3,4-dimethoxypyridine
2-(chloromethyl)-3,4-dimethoxypyridine
Conditions | Yield |
---|---|
With thionyl chloride In dichloromethane | 88% |
With thionyl chloride In dichloromethane | 88% |
With thionyl chloride In dichloromethane at 25℃; for 2h; |
3,4-dimethoxy-2-methylpyridine N-oxide
2-(chloromethyl)-3,4-dimethoxypyridine
Conditions | Yield |
---|---|
Stage #1: 3,4-dimethoxy-2-methylpyridine N-oxide With p-toluenesulfonyl chloride In dichloromethane at 20℃; for 1h; Stage #2: With triethylamine In dichloromethane at 20℃; for 2h; | |
Multi-step reaction with 3 steps 1: AcOH / 120 °C 2: 2N aq. NaOH / methanol / 2 h / 25 °C 3: SOCl2 / CH2Cl2 / 2 h / 25 °C View Scheme |
2-acetoxymethyl-3,4-dimethoxypyridine
2-(chloromethyl)-3,4-dimethoxypyridine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 2N aq. NaOH / methanol / 2 h / 25 °C 2: SOCl2 / CH2Cl2 / 2 h / 25 °C View Scheme |
vanillin
2-(chloromethyl)-3,4-dimethoxypyridine
Conditions | Yield |
---|---|
With potassium carbonate; potassium iodide In acetone at 20℃; for 20h; | 98% |
4-nitro-phenol
2-(chloromethyl)-3,4-dimethoxypyridine
Conditions | Yield |
---|---|
With sodium hydroxide In ethanol at 20℃; for 3h; | 95.1% |
C14H10N4OS2
2-(chloromethyl)-3,4-dimethoxypyridine
C30H28N6O5S2
Conditions | Yield |
---|---|
With sodium hydroxide In methanol for 3h; Reflux; | 90.7% |
2-(chloromethyl)-3,4-dimethoxypyridine
5-(difluoromethoxy)-2-mercapto-1H-benzimidazole
pantoprazole sulfide
Conditions | Yield |
---|---|
With sodium hydroxide In water; isopropyl alcohol at 20℃; for 3h; | 87.8% |
With sodium hydroxide In water Flow reactor; |
Conditions | Yield |
---|---|
With sodium hydroxide In water; acetone at 50℃; for 15h; | 85% |
Conditions | Yield |
---|---|
With sodium hydroxide In water; acetone at 25 - 30℃; for 15h; | 85% |
3-Cyano-4,6-dimethyl-2(1H)-pyridon
2-(chloromethyl)-3,4-dimethoxypyridine
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine; zinc(II) oxide; zinc(II) chloride In 1,4-dioxane at 110℃; Inert atmosphere; | 80% |
(4-acetylaminophenyl)boronic acid
2-(chloromethyl)-3,4-dimethoxypyridine
C16H18N2O3
Conditions | Yield |
---|---|
With potassium phosphate; C12H10ClNPd*C16H21O3P In tetrahydrofuran; water at 60℃; for 20h; | 74% |
1-(phenylsulfinyl)acetophenone
2-(chloromethyl)-3,4-dimethoxypyridine
Conditions | Yield |
---|---|
With potassium carbonate In acetone at 25 - 57℃; for 20h; Inert atmosphere; | 60% |
diphenylmethylisothiouronium bromide
2-(chloromethyl)-3,4-dimethoxypyridine
Conditions | Yield |
---|---|
With potassium carbonate In methanol at 20℃; | 59% |
5-((7-methoxynaphthalen-1-yl)methyl)-1H-tetrazole
2-(chloromethyl)-3,4-dimethoxypyridine
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 50 - 55℃; | 55% |
2-mercaptothieno<3,4-d>imidazole
2-(chloromethyl)-3,4-dimethoxypyridine
2-(3,4-Dimethoxy-pyridin-2-ylmethylsulfanyl)-1H-thieno[3,4-d]imidazole
Conditions | Yield |
---|---|
With sodium methylate In methanol at 65℃; for 1h; | 27% |
2-(chloromethyl)-3,4-dimethoxypyridine
Benzimidazol-2-thiol
A
2-methylsulfanylbenzimidazole
B
2-[(3,4-dimethoxy-2-pyridyl)methylthio]-1H-benzimidazole
Conditions | Yield |
---|---|
In methanol Heating; |
2-(chloromethyl)-3,4-dimethoxypyridine
triethyl phosphite
diethyl [3,4-dimethoxypyridin-2-ylmethylene]phosphonate
Conditions | Yield |
---|---|
With tetra-(n-butyl)ammonium iodide at 110 - 130℃; Michaelis-Arbuzov reaction; |
2-(chloromethyl)-3,4-dimethoxypyridine
(E)-2-aza-2',5,5',6-tetramethoxystilbene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: tetrabutylammonium iodide / 110 - 130 °C 2: sodium hydride / dimethylformamide / 20 °C View Scheme |
2-(chloromethyl)-3,4-dimethoxypyridine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: tetrabutylammonium iodide / 110 - 130 °C 2: sodium hydride / dimethylformamide / 20 °C View Scheme |
2-(chloromethyl)-3,4-dimethoxypyridine
(E)-2-aza-3',5,5',6-tetramethoxystilbene
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: tetrabutylammonium iodide / 110 - 130 °C 2: sodium hydride / dimethylformamide / 20 °C View Scheme |
2-(chloromethyl)-3,4-dimethoxypyridine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: tetrabutylammonium iodide / 110 - 130 °C 2: sodium hydride / dimethylformamide / 20 °C 3: 98.9 percent / boron tribromide / CH2Cl2 / 25 - 35 °C View Scheme |
2-(chloromethyl)-3,4-dimethoxypyridine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: tetrabutylammonium iodide / 110 - 130 °C 2: sodium hydride / dimethylformamide / 20 °C 3: 99.7 percent / boron tribromide / CH2Cl2 / 25 - 35 °C View Scheme |
2-(chloromethyl)-3,4-dimethoxypyridine
2-(3,4-Dimethoxy-pyridin-2-ylmethanesulfinyl)-1H-thieno[3,4-d]imidazole
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 27 percent / NaOMe / methanol / 1 h / 65 °C 2: 60 percent / aq. sodium bicarbonate, m-chloroperbenzoic acid / CH2Cl2 / 0.17 h / 0 °C View Scheme |
2-(chloromethyl)-3,4-dimethoxypyridine
Conditions | Yield |
---|---|
With 2-nitropropane; sodium In methanol at 0 - 70℃; for 25.5h; |
2-(chloromethyl)-3,4-dimethoxypyridine
5-(difluoromethoxy)-2-mercapto-1H-benzimidazole
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: sodium hydroxide / water / Flow reactor 2: sodium hypochlorite; sodium hydroxide / water; acetonitrile / Flow reactor View Scheme |
2-(chloromethyl)-3,4-dimethoxypyridine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: sodium azide / N,N-dimethyl-formamide / 1 h / 20 - 100 °C 2: copper(l) iodide / acetonitrile / 1 h / Reflux 3: ethanol / Reflux View Scheme |
2-(chloromethyl)-3,4-dimethoxypyridine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: sodium azide / N,N-dimethyl-formamide / 1 h / 20 - 100 °C 2: copper(l) iodide / acetonitrile / 1 h / Reflux 3: ethanol / 0.5 h / Reflux View Scheme |
2-(chloromethyl)-3,4-dimethoxypyridine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: sodium azide / N,N-dimethyl-formamide / 1 h / 20 - 100 °C 2: copper(l) iodide / acetonitrile / 1 h / Reflux 3: ethanol / 0.5 h / Reflux View Scheme |
2-(chloromethyl)-3,4-dimethoxypyridine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: sodium azide / N,N-dimethyl-formamide / 1 h / 20 - 100 °C 2: copper(l) iodide / acetonitrile / 1 h / Reflux 3: ethanol / 0.5 h / Reflux View Scheme |
2-(chloromethyl)-3,4-dimethoxypyridine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: sodium azide / N,N-dimethyl-formamide / 1 h / 20 - 100 °C 2: copper(l) iodide / acetonitrile / 1 h / Reflux 3: ethanol / 0.5 h / Reflux View Scheme |
The Pyridine,2-(chloromethyl)-3,4-dimethoxy-, with the CAS registry number 169905-10-6, is also known as 2-Chloromethyl-3,4-dimethoxy pyridine hydrochloride. This chemical's molecular formula is C8H10ClNO2 and molecular weight is 187.6235. Its systematic name is called 2-(chloromethyl)-3,4-dimethoxypyridine.
Physical properties of Pyridine,2-(chloromethyl)-3,4-dimethoxy-: (1)ACD/LogP: 1.52; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 1.49; (4)ACD/LogD (pH 7.4): 1.52; (5)ACD/BCF (pH 5.5): 7.81; (6)ACD/BCF (pH 7.4): 8.47; (7)ACD/KOC (pH 5.5): 148.11; (8)ACD/KOC (pH 7.4): 160.57; (9)#H bond acceptors: 3; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 3; (12)Index of Refraction: 1.511; (13)Molar Refractivity: 47.46 cm3; (14)Molar Volume: 158.3 cm3; (15)Surface Tension: 36.7 dyne/cm; (16)Density: 1.184 g/cm3; (17)Flash Point: 109.7 °C; (18)Enthalpy of Vaporization: 47.54 kJ/mol; (19)Boiling Point: 257.8 °C at 760 mmHg; (20)Vapour Pressure: 0.0229 mmHg at 25°C.
You can still convert the following datas into molecular structure:
(1)SMILES: ClCc1nccc(OC)c1OC
(2)InChI: InChI=1/C8H10ClNO2/c1-11-7-3-4-10-6(5-9)8(7)12-2/h3-4H,5H2,1-2H3
(3)InChIKey: ZWFCXDBCXGDDOM-UHFFFAOYAV
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