Product Name

  • Name

    2-CHLOROMETHYL-3,4-DIMETHOXY PYRIDINE HYDROCHLORIDE

  • EINECS
  • CAS No. 169905-10-6
  • Article Data4
  • CAS DataBase
  • Density 1.185 g/cm3
  • Solubility
  • Melting Point 155 °C (dec.)(lit.)
  • Formula C8H10ClNO2
  • Boiling Point 257.8 °C at 760 mmHg
  • Molecular Weight 187.626
  • Flash Point 109.7 °C
  • Transport Information
  • Appearance
  • Safety 26-36/37/39-61
  • Risk Codes  Xn,N:;
  • Molecular Structure Molecular Structure of 169905-10-6 (2-CHLOROMETHYL-3,4-DIMETHOXY PYRIDINE HYDROCHLORIDE)
  • Hazard Symbols R21/22-38-41-43-48/22-51/53:;
  • Synonyms 2-CHLOROMETHYL-3,4-DIMETHOXY PYRIDINE;2-(CHLOROMETHYL)-3,4-DIMETHOXY PYRIDINE HCL;2-CHLOROMETHYL-3,4-DIMETHOXY PYRIDINE HYDROCHLORIDE;Pyridine, 2-(chloromethyl)-3,4-dimethoxy- (9CI);2-(ChloroMethyl)-3;4-diMethoxypyridine hydrochloride
  • PSA 121.70000
  • LogP 3.26110

Synthetic route

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

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

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

2-(chloromethyl)-3,4-dimethoxypyridine

Conditions
ConditionsYield
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
102625-99-0

2-acetoxymethyl-3,4-dimethoxypyridine

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

2-(chloromethyl)-3,4-dimethoxypyridine

Conditions
ConditionsYield
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
121-33-5

vanillin

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

2-(chloromethyl)-3,4-dimethoxypyridine

4-((3,4-dimethoxypyridin-2-yl)methoxy)-3-methoxybenzaldehyde

4-((3,4-dimethoxypyridin-2-yl)methoxy)-3-methoxybenzaldehyde

Conditions
ConditionsYield
With potassium carbonate; potassium iodide In acetone at 20℃; for 20h;98%
4-nitro-phenol
100-02-7

4-nitro-phenol

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

2-(chloromethyl)-3,4-dimethoxypyridine

3,4-dimethoxy-2-[(4-nitrophenoxy)methyl]pyridine

3,4-dimethoxy-2-[(4-nitrophenoxy)methyl]pyridine

Conditions
ConditionsYield
With sodium hydroxide In ethanol at 20℃; for 3h;95.1%
C14H10N4OS2
1166385-86-9

C14H10N4OS2

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

2-(chloromethyl)-3,4-dimethoxypyridine

C30H28N6O5S2
1166385-45-0

C30H28N6O5S2

Conditions
ConditionsYield
With sodium hydroxide In methanol for 3h; Reflux;90.7%
2-(chloromethyl)-3,4-dimethoxypyridine
169905-10-6

2-(chloromethyl)-3,4-dimethoxypyridine

5-(difluoromethoxy)-2-mercapto-1H-benzimidazole
97963-62-7

5-(difluoromethoxy)-2-mercapto-1H-benzimidazole

pantoprazole sulfide
102625-64-9

pantoprazole sulfide

Conditions
ConditionsYield
With sodium hydroxide In water; isopropyl alcohol at 20℃; for 3h;87.8%
With sodium hydroxide In water Flow reactor;
desmethyl dibenzimidazole
884330-09-0

desmethyl dibenzimidazole

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

2-(chloromethyl)-3,4-dimethoxypyridine

C26H27N5O2

C26H27N5O2

Conditions
ConditionsYield
With sodium hydroxide In water; acetone at 50℃; for 15h;85%
C40H30N6S
1247013-51-9

C40H30N6S

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

2-(chloromethyl)-3,4-dimethoxypyridine

C48H39N7O2S
1247013-53-1

C48H39N7O2S

Conditions
ConditionsYield
With sodium hydroxide In water; acetone at 25 - 30℃; for 15h;85%
3-Cyano-4,6-dimethyl-2(1H)-pyridon
769-28-8

3-Cyano-4,6-dimethyl-2(1H)-pyridon

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

2-(chloromethyl)-3,4-dimethoxypyridine

2-((3,4-dimethoxypyridin-2-yl)methoxy)-4,6-dimethylnicotinonitrile

2-((3,4-dimethoxypyridin-2-yl)methoxy)-4,6-dimethylnicotinonitrile

Conditions
ConditionsYield
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
101251-09-6

(4-acetylaminophenyl)boronic acid

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

2-(chloromethyl)-3,4-dimethoxypyridine

C16H18N2O3
1416422-97-3

C16H18N2O3

Conditions
ConditionsYield
With potassium phosphate; C12H10ClNPd*C16H21O3P In tetrahydrofuran; water at 60℃; for 20h;74%
1-(phenylsulfinyl)acetophenone
6099-23-6

1-(phenylsulfinyl)acetophenone

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

2-(chloromethyl)-3,4-dimethoxypyridine

2-benzenesulfinylmethyl-3,4-dimethoxypyridine

2-benzenesulfinylmethyl-3,4-dimethoxypyridine

Conditions
ConditionsYield
With potassium carbonate In acetone at 25 - 57℃; for 20h; Inert atmosphere;60%
diphenylmethylisothiouronium bromide
90280-15-2

diphenylmethylisothiouronium bromide

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

2-(chloromethyl)-3,4-dimethoxypyridine

2-((benzhydrylthio)methyl)-3,4-dimethoxypyridine

2-((benzhydrylthio)methyl)-3,4-dimethoxypyridine

Conditions
ConditionsYield
With potassium carbonate In methanol at 20℃;59%
5-((7-methoxynaphthalen-1-yl)methyl)-1H-tetrazole
1425498-90-3

5-((7-methoxynaphthalen-1-yl)methyl)-1H-tetrazole

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

2-(chloromethyl)-3,4-dimethoxypyridine

3,4-dimethoxy-2-((5-((7-methoxynaphthalen-1-yl)methyl)-1H-tetrazol-1-yl)methyl)pyridine

3,4-dimethoxy-2-((5-((7-methoxynaphthalen-1-yl)methyl)-1H-tetrazol-1-yl)methyl)pyridine

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 50 - 55℃;55%
2-mercaptothieno<3,4-d>imidazole
90070-09-0

2-mercaptothieno<3,4-d>imidazole

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

2-(chloromethyl)-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
With sodium methylate In methanol at 65℃; for 1h;27%
2-(chloromethyl)-3,4-dimethoxypyridine
169905-10-6

2-(chloromethyl)-3,4-dimethoxypyridine

Benzimidazol-2-thiol
134469-07-1

Benzimidazol-2-thiol

A

2-methylsulfanylbenzimidazole
7152-24-1

2-methylsulfanylbenzimidazole

B

2-[(3,4-dimethoxy-2-pyridyl)methylthio]-1H-benzimidazole
107512-18-5

2-[(3,4-dimethoxy-2-pyridyl)methylthio]-1H-benzimidazole

Conditions
ConditionsYield
In methanol Heating;
2-(chloromethyl)-3,4-dimethoxypyridine
169905-10-6

2-(chloromethyl)-3,4-dimethoxypyridine

triethyl phosphite
122-52-1

triethyl phosphite

diethyl [3,4-dimethoxypyridin-2-ylmethylene]phosphonate
895537-11-8

diethyl [3,4-dimethoxypyridin-2-ylmethylene]phosphonate

Conditions
ConditionsYield
With tetra-(n-butyl)ammonium iodide at 110 - 130℃; Michaelis-Arbuzov reaction;
2-(chloromethyl)-3,4-dimethoxypyridine
169905-10-6

2-(chloromethyl)-3,4-dimethoxypyridine

(E)-2-aza-2',5,5',6-tetramethoxystilbene
895537-14-1

(E)-2-aza-2',5,5',6-tetramethoxystilbene

Conditions
ConditionsYield
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
169905-10-6

2-(chloromethyl)-3,4-dimethoxypyridine

(E)-2-aza-2',4',5,6-tetramethoxystilbene

(E)-2-aza-2',4',5,6-tetramethoxystilbene

Conditions
ConditionsYield
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
169905-10-6

2-(chloromethyl)-3,4-dimethoxypyridine

(E)-2-aza-3',5,5',6-tetramethoxystilbene
895537-12-9

(E)-2-aza-3',5,5',6-tetramethoxystilbene

Conditions
ConditionsYield
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
169905-10-6

2-(chloromethyl)-3,4-dimethoxypyridine

(E)-2-aza-3',5,5',6-tetrahydroxystilbene

(E)-2-aza-3',5,5',6-tetrahydroxystilbene

Conditions
ConditionsYield
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
169905-10-6

2-(chloromethyl)-3,4-dimethoxypyridine

(E)-2-aza-2',5,5',6-tetrahydroxystilbene

(E)-2-aza-2',5,5',6-tetrahydroxystilbene

Conditions
ConditionsYield
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
169905-10-6

2-(chloromethyl)-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 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
169905-10-6

2-(chloromethyl)-3,4-dimethoxypyridine

3,4-dimethoxy-2-formylpyridine

3,4-dimethoxy-2-formylpyridine

Conditions
ConditionsYield
With 2-nitropropane; sodium In methanol at 0 - 70℃; for 25.5h;
2-(chloromethyl)-3,4-dimethoxypyridine
169905-10-6

2-(chloromethyl)-3,4-dimethoxypyridine

5-(difluoromethoxy)-2-mercapto-1H-benzimidazole
97963-62-7

5-(difluoromethoxy)-2-mercapto-1H-benzimidazole

pantoprazole

pantoprazole

Conditions
ConditionsYield
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
169905-10-6

2-(chloromethyl)-3,4-dimethoxypyridine

(E)-N’-(4-(1-((3,4-dimethoxypyridin-2-yl)methyl)-1H-1,2,3-triazol-4-yl)benzylidene)benzohydrazide

(E)-N’-(4-(1-((3,4-dimethoxypyridin-2-yl)methyl)-1H-1,2,3-triazol-4-yl)benzylidene)benzohydrazide

Conditions
ConditionsYield
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
169905-10-6

2-(chloromethyl)-3,4-dimethoxypyridine

(E)-N’-(4-(1-((3,4-dimethoxypyridin-2-yl)methyl)-1H-1,2,3-triazol-4-yl)benzylidene)-4-hydroxybenzohydrazide

(E)-N’-(4-(1-((3,4-dimethoxypyridin-2-yl)methyl)-1H-1,2,3-triazol-4-yl)benzylidene)-4-hydroxybenzohydrazide

Conditions
ConditionsYield
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
169905-10-6

2-(chloromethyl)-3,4-dimethoxypyridine

(E)-N’-(4-(1-((3,4-dimethoxypyridin-2-yl)methyl)-1H-1,2,3-triazol-4-yl)benzylidene)-4-methoxybenzohydrazide

(E)-N’-(4-(1-((3,4-dimethoxypyridin-2-yl)methyl)-1H-1,2,3-triazol-4-yl)benzylidene)-4-methoxybenzohydrazide

Conditions
ConditionsYield
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
169905-10-6

2-(chloromethyl)-3,4-dimethoxypyridine

(E)-N’-(4-(1-((3,4-dimethoxypyridin-2-yl)methyl)-1H-1,2,3-triazol-4-yl)benzylidene)-4-(methylsulfonyl)benzohydrazide

(E)-N’-(4-(1-((3,4-dimethoxypyridin-2-yl)methyl)-1H-1,2,3-triazol-4-yl)benzylidene)-4-(methylsulfonyl)benzohydrazide

Conditions
ConditionsYield
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
169905-10-6

2-(chloromethyl)-3,4-dimethoxypyridine

(E)-N’-(4-(1-((3,4-dimethoxypyridin-2-yl)methyl)-1H-1,2,3-triazol-4-yl)benzylidene)-3,4,5-trimethoxybenzohydrazide

(E)-N’-(4-(1-((3,4-dimethoxypyridin-2-yl)methyl)-1H-1,2,3-triazol-4-yl)benzylidene)-3,4,5-trimethoxybenzohydrazide

Conditions
ConditionsYield
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 Specification

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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