Product Name

  • Name

    3,4-Dimethoxy-2-pyridinemethanol

  • EINECS
  • CAS No. 72830-08-1
  • Article Data10
  • CAS DataBase
  • Density 1.171 g/cm3
  • Solubility
  • Melting Point
  • Formula C8H11NO3
  • Boiling Point 275.516 °C at 760 mmHg
  • Molecular Weight 169.18
  • Flash Point 120.428 °C
  • Transport Information
  • Appearance
  • Safety
  • Risk Codes
  • Molecular Structure Molecular Structure of 72830-08-1 (3,4-Dimethoxy-2-pyridinemethanol)
  • Hazard Symbols IrritantXi
  • Synonyms 2-Hydroxymethyl-3,4-dimethoxypyridine;3,4-Dimethoxy-2-(hydroxymethyl)pyridine;
  • PSA 51.58000
  • LogP 0.59110

Synthetic route

3,4-dimethoxy-2-methylpyridine N-oxide
72830-07-0

3,4-dimethoxy-2-methylpyridine N-oxide

2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

Conditions
ConditionsYield
With acetic anhydride for 4h; Reflux;91%
Stage #1: 3,4-dimethoxy-2-methylpyridine N-oxide With acetic anhydride at 90℃; for 2h;
Stage #2: With sodium hydroxide In water at 80℃; for 2h;
76%
Multi-step reaction with 2 steps
1: 4 h / 100 °C
2: 2 M NaOH / 1 h / 100 °C
View Scheme
Multi-step reaction with 2 steps
1: 2 h / 90 °C
2: 2 N aq. NaOH / 2 h / 80 °C
View Scheme
Multi-step reaction with 2 steps
1: AcOH / 120 °C
2: 2N aq. NaOH / methanol / 2 h / 25 °C
View Scheme
2-acetoxymethyl-3,4-dimethoxypyridine
102625-99-0

2-acetoxymethyl-3,4-dimethoxypyridine

2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

Conditions
ConditionsYield
With sodium hydroxide at 80℃; for 2h; Yield given;
With sodium hydroxide In methanol at 25℃; for 2h;
With sodium hydroxide at 100℃; for 1h;
With sodium hydroxide In Petroleum ether
With sodium hydroxide In Petroleum ether
Maltol
118-71-8

Maltol

2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

Conditions
ConditionsYield
Multi-step reaction with 7 steps
1: 68 percent / K2CO3 / acetone / 19 h / Heating
2: 77 percent / conc. ammonia / 3 h / 110 °C
3: 85 percent / POCl3 / 10 h / Heating
4: NaOMe / 10 h / Heating
5: 98 percent / 84percent m-CPBA / CH2Cl2 / 4 h / Ambient temperature
6: 4 h / 100 °C
7: 2 M NaOH / 1 h / 100 °C
View Scheme
Multi-step reaction with 4 steps
1.1: ammonium hydroxide / 2 h / 40 °C
1.2: 10 h / 40 °C / Reflux
2.1: potassium hydroxide / water / 20 h / 10 - 20 °C
3.1: acetic acid; sodium tungstate; dihydrogen peroxide / 4 h / 40 - 95 °C
4.1: acetic anhydride / 4 h / Reflux
View Scheme
3-methoxy-2-methyl-4-pyrone
4780-14-7

3-methoxy-2-methyl-4-pyrone

2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

Conditions
ConditionsYield
Multi-step reaction with 6 steps
1: 77 percent / conc. ammonia / 3 h / 110 °C
2: 85 percent / POCl3 / 10 h / Heating
3: NaOMe / 10 h / Heating
4: 98 percent / 84percent m-CPBA / CH2Cl2 / 4 h / Ambient temperature
5: 4 h / 100 °C
6: 2 M NaOH / 1 h / 100 °C
View Scheme
2-methyl-3-methoxy-4(1H)-pyridinone
76015-11-7

2-methyl-3-methoxy-4(1H)-pyridinone

2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

Conditions
ConditionsYield
Multi-step reaction with 5 steps
1: 85 percent / POCl3 / 10 h / Heating
2: NaOMe / 10 h / Heating
3: 98 percent / 84percent m-CPBA / CH2Cl2 / 4 h / Ambient temperature
4: 4 h / 100 °C
5: 2 M NaOH / 1 h / 100 °C
View Scheme
Multi-step reaction with 5 steps
1: 96 percent / POCl3 / 18 h / 90 °C
2: 90 percent / 30percent aq. H2O2, AcOH / 24 h / 90 °C
3: 91 percent / NaOMe / 18 h
4: 2 h / 90 °C
5: 2 N aq. NaOH / 2 h / 80 °C
View Scheme
Multi-step reaction with 4 steps
1.1: trichlorophosphate / 18 h / 90 °C / Inert atmosphere
2.1: acetic acid; dihydrogen peroxide / water / 24 h / 90 °C
3.1: methanol / 16 h / 40 °C
4.1: acetic anhydride / 2 h / 90 °C
4.2: 2 h / 80 °C
View Scheme
4-Chloro-3-methoxy-2-methyl-pyridine
107512-34-5

4-Chloro-3-methoxy-2-methyl-pyridine

2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: NaOMe / 10 h / Heating
2: 98 percent / 84percent m-CPBA / CH2Cl2 / 4 h / Ambient temperature
3: 4 h / 100 °C
4: 2 M NaOH / 1 h / 100 °C
View Scheme
Multi-step reaction with 4 steps
1: 90 percent / 30percent aq. H2O2, AcOH / 24 h / 90 °C
2: 91 percent / NaOMe / 18 h
3: 2 h / 90 °C
4: 2 N aq. NaOH / 2 h / 80 °C
View Scheme
Multi-step reaction with 3 steps
1.1: acetic acid; dihydrogen peroxide / water / 24 h / 90 °C
2.1: methanol / 16 h / 40 °C
3.1: acetic anhydride / 2 h / 90 °C
3.2: 2 h / 80 °C
View Scheme
3,4-dimethoxy-2-methylpyridine
107512-35-6

3,4-dimethoxy-2-methylpyridine

2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 98 percent / 84percent m-CPBA / CH2Cl2 / 4 h / Ambient temperature
2: 4 h / 100 °C
3: 2 M NaOH / 1 h / 100 °C
View Scheme
Multi-step reaction with 2 steps
1: acetic acid; sodium tungstate; dihydrogen peroxide / 4 h / 40 - 95 °C
2: acetic anhydride / 4 h / Reflux
View Scheme
3-methoxy-2-methyl-4-nitropyridine 1-oxide
15931-25-6

3-methoxy-2-methyl-4-nitropyridine 1-oxide

2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 88 percent / NaOMe / 16 h / 40 °C
2: 2 h / 90 °C
3: 2 N aq. NaOH / 2 h / 80 °C
View Scheme
3-methoxy-2-methylpyridine 1-oxide
35392-65-5

3-methoxy-2-methylpyridine 1-oxide

2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: 58 percent / 98percent HNO3 / acetic acid / 33 h / 80 °C
2: 88 percent / NaOMe / 16 h / 40 °C
3: 2 h / 90 °C
4: 2 N aq. NaOH / 2 h / 80 °C
View Scheme
4-chloro-3-methoxy-2-methylpyridine N-oxide
122307-41-9

4-chloro-3-methoxy-2-methylpyridine N-oxide

2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 91 percent / NaOMe / 18 h
2: 2 h / 90 °C
3: 2 N aq. NaOH / 2 h / 80 °C
View Scheme
Multi-step reaction with 2 steps
1.1: methanol / 16 h / 40 °C
2.1: acetic anhydride / 2 h / 90 °C
2.2: 2 h / 80 °C
View Scheme
3-fluoro-2-methyl-4-nitropyridine 1-oxide
15931-17-6

3-fluoro-2-methyl-4-nitropyridine 1-oxide

2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

Conditions
ConditionsYield
In acetic anhydride
5-(difluoromethoxy)-2-[[(3,4-dimethoxy-2-pyridyl)methyl]sulfinyl]-1H-benzimidazole
102625-70-7

5-(difluoromethoxy)-2-[[(3,4-dimethoxy-2-pyridyl)methyl]sulfinyl]-1H-benzimidazole

A

5-difluoromethoxy-3H-benzimidazole-2-thione

5-difluoromethoxy-3H-benzimidazole-2-thione

B

2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

Conditions
ConditionsYield
With water at 40℃; for 5844h;
acetic anhydride
108-24-7

acetic anhydride

3,4-dimethoxy-2-methylpyridine N-oxide
72830-07-0

3,4-dimethoxy-2-methylpyridine N-oxide

acetic acid
64-19-7

acetic acid

2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

Conditions
ConditionsYield
Stage #1: 3,4-dimethoxy-2-methylpyridine N-oxide ; acetic acid at 75℃; Large scale;
Stage #2: acetic anhydride at 80 - 85℃; under 690.069 Torr; for 16h; Large scale;
Stage #3: With sodium hydroxide at 18 - 55℃; for 2h; pH=12 - 13; Temperature; Large scale;
3-hydroxy-2-methylpyrid-4-one
17184-19-9

3-hydroxy-2-methylpyrid-4-one

2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: potassium hydroxide / water / 20 h / 10 - 20 °C
2: acetic acid; sodium tungstate; dihydrogen peroxide / 4 h / 40 - 95 °C
3: acetic anhydride / 4 h / Reflux
View Scheme
2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

2-Chloromethyl-3,4-dimethoxy-pyridine; hydrochloride
72830-09-2

2-Chloromethyl-3,4-dimethoxy-pyridine; hydrochloride

Conditions
ConditionsYield
With thionyl chloride In dichloromethane for 2h;100%
With bis(trichloromethyl) carbonate; Triphenylphosphine oxide In toluene at 20 - 60℃; for 4h;98%
With thionyl chloride In dichloromethane at 0 - 5℃; for 2h;93%
2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

2-(chloromethyl)-3,4-dimethoxypyridine
169905-10-6

2-(chloromethyl)-3,4-dimethoxypyridine

Conditions
ConditionsYield
With thionyl chloride In dichloromethane88%
With thionyl chloride In dichloromethane88%
With thionyl chloride In dichloromethane at 25℃; for 2h;
2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

2-(3,4-Dimethoxy-pyridin-2-ylmethylsulfanyl)-5,6-difluoro-1H-benzoimidazole

2-(3,4-Dimethoxy-pyridin-2-ylmethylsulfanyl)-5,6-difluoro-1H-benzoimidazole

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 100 percent / SOCl2 / CH2Cl2 / 2 h
2: 1.) aq. NaOH / methanol
View Scheme
2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

2-(3,4-Dimethoxy-pyridin-2-ylmethanesulfinyl)-5,6-difluoro-1H-benzoimidazole

2-(3,4-Dimethoxy-pyridin-2-ylmethanesulfinyl)-5,6-difluoro-1H-benzoimidazole

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 100 percent / SOCl2 / CH2Cl2 / 2 h
2: 1.) aq. NaOH / methanol
3: m-CPBA, aq. NaHCO3 / CH2Cl2 / 0.17 h
View Scheme
2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

pantoprazole sulfide
102625-64-9

pantoprazole sulfide

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 93 percent / SOCl2 / CH2Cl2 / 2 h / 0 - 5 °C
2: 2 N aq. NaOH / ethanol / 2 h / 50 °C
View Scheme
2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

5-Difluoromethoxy-2-(3,4-dimethoxy-pyridin-2-ylmethylsulfanyl)-6-fluoro-1H-benzoimidazole
138786-84-2

5-Difluoromethoxy-2-(3,4-dimethoxy-pyridin-2-ylmethylsulfanyl)-6-fluoro-1H-benzoimidazole

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 93 percent / SOCl2 / CH2Cl2 / 2 h / 0 - 5 °C
2: 2 N aq. NaOH / ethanol / 2 h / 50 °C
View Scheme
2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

5-difluoromethoxy-6-methoxy-2-[(3,4-dimethoxy-pyridin-2-yl)methylthio]-1H-benzimidazole
102625-65-0

5-difluoromethoxy-6-methoxy-2-[(3,4-dimethoxy-pyridin-2-yl)methylthio]-1H-benzimidazole

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 93 percent / SOCl2 / CH2Cl2 / 2 h / 0 - 5 °C
2: 2 N aq. NaOH / ethanol / 2 h / 50 °C
View Scheme
2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

2,2-difluoro-6-[(3,4-dimethoxy-2-pyridyl)methylthio]-5H-[1,3]-dioxolo-[4,5-f]benzimidazole
102625-75-2

2,2-difluoro-6-[(3,4-dimethoxy-2-pyridyl)methylthio]-5H-[1,3]-dioxolo-[4,5-f]benzimidazole

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 93 percent / SOCl2 / CH2Cl2 / 2 h / 0 - 5 °C
2: aq. NaOH / ethanol / 4 h / 60 °C
View Scheme
2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

5-(difluoromethoxy)-2-[[(3,4-dimethoxy-2-pyridyl)methyl]sulfinyl]-1H-benzimidazole
102625-70-7

5-(difluoromethoxy)-2-[[(3,4-dimethoxy-2-pyridyl)methyl]sulfinyl]-1H-benzimidazole

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 93 percent / SOCl2 / CH2Cl2 / 2 h / 0 - 5 °C
2: 2 N aq. NaOH / ethanol / 2 h / 50 °C
3: 85 percent / m-chloroperbenzoic acid / CH2Cl2 / 0.5 h / -30 °C
View Scheme
2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

2-[(3,4-dimethoxy-pyridin-2-yl)methylthio]-5-(1,1,2,2-tetrafluoroethoxy)-1H-benzimidazole
102625-63-8

2-[(3,4-dimethoxy-pyridin-2-yl)methylthio]-5-(1,1,2,2-tetrafluoroethoxy)-1H-benzimidazole

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 93 percent / SOCl2 / CH2Cl2 / 2 h / 0 - 5 °C
2: 2 N aq. NaOH / ethanol / 2 h / 50 °C
View Scheme
2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

2-[(3,4-dimethoxy-pyridin-2-yl)methylthio]-5-(2,2,2-trifluoroethoxy)-1H-benzimidazole
138786-82-0

2-[(3,4-dimethoxy-pyridin-2-yl)methylthio]-5-(2,2,2-trifluoroethoxy)-1H-benzimidazole

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 93 percent / SOCl2 / CH2Cl2 / 2 h / 0 - 5 °C
2: 2 N aq. NaOH / ethanol / 2 h / 50 °C
View Scheme
2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

6-(3,4-Dimethoxy-pyridin-2-ylmethanesulfinyl)-2,2-difluoro-5H-[1,3]dioxolo[4',5':4,5]benzo[1,2-d]imidazole
102625-81-0

6-(3,4-Dimethoxy-pyridin-2-ylmethanesulfinyl)-2,2-difluoro-5H-[1,3]dioxolo[4',5':4,5]benzo[1,2-d]imidazole

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 93 percent / SOCl2 / CH2Cl2 / 2 h / 0 - 5 °C
2: aq. NaOH / ethanol / 4 h / 60 °C
3: 85 percent / m-chloroperbenzoic acid / CH2Cl2 / 0.5 h / -30 °C
View Scheme
2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

5-Difluoromethoxy-2-(3,4-dimethoxy-pyridin-2-ylmethanesulfinyl)-6-fluoro-1H-benzoimidazole
138786-72-8

5-Difluoromethoxy-2-(3,4-dimethoxy-pyridin-2-ylmethanesulfinyl)-6-fluoro-1H-benzoimidazole

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 93 percent / SOCl2 / CH2Cl2 / 2 h / 0 - 5 °C
2: 2 N aq. NaOH / ethanol / 2 h / 50 °C
3: 73 percent / m-chloroperbenzoic acid / CH2Cl2 / 0.5 h / -30 °C
View Scheme
2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

5-difluoromethoxy-6-methoxy-2-[(3,4-dimethoxy-pyridin-2-yl)methylsulfinyl]-1H-benzimidazole
138786-71-7

5-difluoromethoxy-6-methoxy-2-[(3,4-dimethoxy-pyridin-2-yl)methylsulfinyl]-1H-benzimidazole

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 93 percent / SOCl2 / CH2Cl2 / 2 h / 0 - 5 °C
2: 2 N aq. NaOH / ethanol / 2 h / 50 °C
3: 83 percent / m-chloroperbenzoic acid / CH2Cl2 / 0.5 h / -30 °C
View Scheme
2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

2-[(3,4-dimethoxy-pyridin-2-yl)methylsulfinyl]-5-(1,1,2,2-tetrafluoroethoxy)-1H-benzimidazole
102625-69-4

2-[(3,4-dimethoxy-pyridin-2-yl)methylsulfinyl]-5-(1,1,2,2-tetrafluoroethoxy)-1H-benzimidazole

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 93 percent / SOCl2 / CH2Cl2 / 2 h / 0 - 5 °C
2: 2 N aq. NaOH / ethanol / 2 h / 50 °C
3: 66 percent / m-chloroperbenzoic acid / CH2Cl2 / 0.5 h / -30 °C
View Scheme
2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

2-[(3,4-dimethoxy-pyridin-2-yl)methylsulfinyl]-5-(2,2,2-trifluoroethoxy)-1H-benzimidazole
138786-69-3

2-[(3,4-dimethoxy-pyridin-2-yl)methylsulfinyl]-5-(2,2,2-trifluoroethoxy)-1H-benzimidazole

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 93 percent / SOCl2 / CH2Cl2 / 2 h / 0 - 5 °C
2: 2 N aq. NaOH / ethanol / 2 h / 50 °C
3: 87 percent / m-chloroperbenzoic acid / CH2Cl2 / 0.5 h / -30 °C
View Scheme
2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

9-(difluoromethoxy)-3,4-dimethoxy-5H-pyrido<1',2':4,5><1,2,4>thiadiazino<2,3-a>benzimidazol-13-ium hexafluorophosphate
138786-75-1

9-(difluoromethoxy)-3,4-dimethoxy-5H-pyrido<1',2':4,5><1,2,4>thiadiazino<2,3-a>benzimidazol-13-ium hexafluorophosphate

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: 93 percent / SOCl2 / CH2Cl2 / 2 h / 0 - 5 °C
2: 2 N aq. NaOH / ethanol / 2 h / 50 °C
3: 85 percent / m-chloroperbenzoic acid / CH2Cl2 / 0.5 h / -30 °C
4: aq. hexafluorophosphoric acid / methanol / 1.5 h / 0 - 5 °C
View Scheme
2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

10-(difluoromethoxy)-3,4-dimethoxy-5H-pyrido<1',2':4,5><1,2,4>thiadiazino<2,3-a>benzimidazol-13-ium hexafluorophosphate
138786-76-2

10-(difluoromethoxy)-3,4-dimethoxy-5H-pyrido<1',2':4,5><1,2,4>thiadiazino<2,3-a>benzimidazol-13-ium hexafluorophosphate

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: 93 percent / SOCl2 / CH2Cl2 / 2 h / 0 - 5 °C
2: 2 N aq. NaOH / ethanol / 2 h / 50 °C
3: 85 percent / m-chloroperbenzoic acid / CH2Cl2 / 0.5 h / -30 °C
4: aq. hexafluorophosphoric acid / methanol / 1.5 h / 0 - 5 °C
View Scheme
2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

2-(3,4-Dimethoxy-pyridin-2-ylmethylsulfanyl)-1H-thieno[3,4-d]imidazole
122307-42-0

2-(3,4-Dimethoxy-pyridin-2-ylmethylsulfanyl)-1H-thieno[3,4-d]imidazole

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: SOCl2 / CH2Cl2 / 2 h / 25 °C
2: 27 percent / NaOMe / methanol / 1 h / 65 °C
View Scheme
2-hydroxymethyl-3,4-dimethoxypyridine
72830-08-1

2-hydroxymethyl-3,4-dimethoxypyridine

2-(3,4-Dimethoxy-pyridin-2-ylmethanesulfinyl)-1H-thieno[3,4-d]imidazole
122307-43-1

2-(3,4-Dimethoxy-pyridin-2-ylmethanesulfinyl)-1H-thieno[3,4-d]imidazole

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: SOCl2 / CH2Cl2 / 2 h / 25 °C
2: 27 percent / NaOMe / methanol / 1 h / 65 °C
3: 60 percent / aq. sodium bicarbonate, m-chloroperbenzoic acid / CH2Cl2 / 0.17 h / 0 °C
View Scheme

3,4-Dimethoxy-2-pyridinemethanol Chemical Properties

Product Name: 3,4-Dimethoxy-2-pyridinemethanol
Molecular Structure:

Molecular Formula: C8H11NO3
Molecular Weight: 169.1778
Synonyms of 3,4-Dimethoxy-2-pyridinemethanol (CAS NO.72830-08-1): 4-Chloro-2-chloromethyl-3-methoxypyridine hydrochloride ; 4-Chloro-2-chloromethyl-3-methoxypyridine,hydrochloride salt ; 4-Chloro-3-methoxy-2-chloromethylpyridine hcl ; 4-Chloro-3-methoxy-2-chloromethyl pyridine hydrochloride ; 2-Hydroxymethyl-3,4-dimethoxypyridine
CAS NO: 72830-08-1
Product Categories: Pyridines, Pyrimidines, Purines and Pteredines ; Pyridines derivates ; API intermediates 
H bond acceptors: 4
H bond donors: 1
Freely Rotating Bonds: 4
Polar Surface Area: 51.58 Å2
Index of Refraction: 1.523
Molar Refractivity: 44.152 cm3
Molar Volume: 144.478 cm3
Surface Tension: 42.229 dyne/cm
Density: 1.171 g/cm3
Flash Point: 120.428 °C
Enthalpy of Vaporization: 54.292 kJ/mol
Boiling Point: 275.516 °C at 760 mmHg
Vapour Pressure of 3,4-Dimethoxy-2-pyridinemethanol (CAS NO.72830-08-1): 0.002 mmHg at 25°C

3,4-Dimethoxy-2-pyridinemethanol Safety Profile

Hazard Codes of 3,4-Dimethoxy-2-pyridinemethanol (CAS NO.72830-08-1): IrritantXi
Hazard Note: Irritant 

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