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100-69-6

Basic Information
CAS No.: 100-69-6
Name: Pyridine,2-ethenyl-
Molecular Structure:
Molecular Structure of 100-69-6 (Pyridine,2-ethenyl-)
Formula: C7H7N
Molecular Weight: 105.15
Synonyms: Pyridine,2-vinyl- (8CI);2-Ethenylpyridine;2-Pyridylethylene;NSC18255;a-Vinylpyridine;
EINECS: 202-879-8
Density: 0.968 g/cm3
Melting Point: -50 °C
Boiling Point: 160.3 °C at 760 mmHg
Flash Point: 46.7 °C
Solubility: 2.5 g/100 mL (20 °C) in water
Appearance: dark brown liquid with an unpleasant odour
Hazard Symbols: ToxicT,CorrosiveC,FlammableF
Risk Codes: 10-20-25-34-42/43
Safety: 16-23-26-36/37/39-45-28A
Transport Information: UN 3073 6.1/PG 2
PSA: 12.89000
LogP: 1.72460
Synthetic route
1945-84-2

2-ethynylpyridine

100-69-6

2-vinylpyridine

Conditions
ConditionsYield
With hydrogen In toluene at 20℃; under 22801.5 Torr; for 12h; Autoclave; chemoselective reaction;99%
With hydrogen In toluene at 110℃; under 760.051 Torr; for 24h; Schlenk technique;87%
With ammonium formate In N,N-dimethyl-formamide at 80℃; Green chemistry;76%
25877-30-9

diethyl-(2-pyridin-2-yl-ethyl)-amine

100-69-6

2-vinylpyridine

Conditions
ConditionsYield
92.3%
1121-60-4

pyridine-2-carbaldehyde

18107-18-1

diazomethyl-trimethyl-silane

100-69-6

2-vinylpyridine

Conditions
ConditionsYield
With (IMes)CuCl; triphenylphosphine; isopropyl alcohol In 1,4-dioxane; diethyl ether at 60℃; for 16h;86%
109-09-1

2-chloropyridine

7486-35-3

tri-n-butyl(vinyl)tin

100-69-6

2-vinylpyridine

Conditions
ConditionsYield
With cesium fluoride In ethanol; water at 50℃; for 5h; Stille coupling; Inert atmosphere;82%
138428-37-2

2-(pyridin-2-yl)ethyl methanesulfonate

100-69-6

2-vinylpyridine

Conditions
ConditionsYield
With N-benzyl-N,N,N-triethylammonium chloride; sodium hydroxide In water at 40℃; for 2h;80%
With sodium carbonate
593-60-2

Vinyl bromide

81745-83-7

pyridin-2-ylzinc(ll) bromide

100-69-6

2-vinylpyridine

Conditions
ConditionsYield
With tetrakis(triphenylphosphine) palladium(0) In tetrahydrofuran for 6h; Ambient temperature;73%
103-74-2

2-(2-Hydroxyethyl)pyridine

100-69-6

2-vinylpyridine

Conditions
ConditionsYield
With acetic acid for 12h; Heating;70%
With sodium tetrafluoroborate; acetic acid In N,N-dimethyl acetamide at 150℃; for 24h; Reagent/catalyst;64%
With tris(triphenylphosphine)ruthenium(II) chloride; 1,3-bis-(diphenylphosphino)propane; sodium t-butanolate In toluene at 111℃; for 24h; Inert atmosphere;41%
107-13-1

acrylonitrile

74-86-2

acetylene

100-69-6

2-vinylpyridine

Conditions
ConditionsYield
borininato-cobalt-COD catalyst at 120℃; under 38253.1 Torr; for 2h;62%
With (η-1,5-cyclooctadien(<1-6-η-(1-phenylborinato)>cobalt at 120℃; under 38253.1 Torr; for 2.08333h;61.5%
103-74-2

2-(2-Hydroxyethyl)pyridine

501-65-5

diphenyl acetylene

A

100-69-6

2-vinylpyridine

B

3,4-diphenylquinolizin-5-ium tetrafluoroborate

Conditions
ConditionsYield
With sodium tetrafluoroborate; dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; copper diacetate; acetic acid In N,N-dimethyl acetamide at 150℃; for 24h; Time;A 26%
B 53%
4833-24-3

2-ethylpyridine 1-oxide

100-69-6

2-vinylpyridine

Conditions
ConditionsYield
at 800℃; under 0.1 Torr;45%
82198-70-7

1,2-bis(2-pyridyl)ethane N-oxide

A

110-86-1

pyridine

B

100-69-6

2-vinylpyridine

C

109-06-8

α-picoline

D

4916-40-9

1,2-bis(pyridin-2-yl)ethane

E

1437-15-6

1,2-bis(2-pyridyl)ethylene

Conditions
ConditionsYield
at 800℃; under 0.05 - 0.2 Torr; Product distribution; Mechanism;A 11%
B 39%
C 11%
D 7%
E 20%
56983-98-3

(2-pyridyl)acetaldoxime

A

110-86-1

pyridine

B

100-69-6

2-vinylpyridine

C

109-06-8

α-picoline

D

100-71-0

2-Ethylpyridine

E

73177-35-2

2-methyl-1H-pyrrolo<3,2-b>pyridine

F

4916-40-9

1,2-bis(pyridin-2-yl)ethane

Conditions
ConditionsYield
at 800℃; under 0.001 - 0.01 Torr; approximate contact time: 0.002-0.03 s;A 18%
B 5%
C 32%
D 11%
E 4%
F 32%
109-06-8

α-picoline

67-56-1

methanol

A

100-69-6

2-vinylpyridine

B

108-48-5

2,6-dimethylpyridine

C

100-71-0

2-Ethylpyridine

D

108-47-4

2,4-lutidine

Conditions
ConditionsYield
Cs exchanged zeolite at 450℃; Product distribution; investigation of the heterogeneous vapor-phase alkylation of α-picoline with methanol over Na+, K+, Rb+, or Cs+ exchanged X- or Y-type zeolite in an atmosphere of nitrogen;A 3.1%
B 7.3%
C 30.2%
D 3.6%
931-19-1

2-methylpyridine N-oxide

A

110-86-1

pyridine

B

100-69-6

2-vinylpyridine

C

109-06-8

α-picoline

D

1132-37-2

bis(2-pyridyl)methane

E

4916-40-9

1,2-bis(pyridin-2-yl)ethane

F

1437-15-6

1,2-bis(2-pyridyl)ethylene

Conditions
ConditionsYield
at 800℃; under 0.1 - 1 Torr; Product distribution; Mechanism; other temperatures; other pressure; different carriers; various alkyl derivatives of pyridine N-oxides;A 24%
B 7%
C 17%
D 8%
E 26%
F 11%
54856-82-5

3-methyl-[1,2,3]triazolo[1,5-a]pyridine

100-69-6

2-vinylpyridine

Conditions
ConditionsYield
With palladium on activated charcoal In ethanol at 150℃; for 24h; Autoclave;23%
110-86-1

pyridine

67-56-1

methanol

A

100-69-6

2-vinylpyridine

B

109-06-8

α-picoline

C

108-89-4

picoline

D

100-71-0

2-Ethylpyridine

E

536-75-4

4-Ethylpyridine

F

108-99-6

3-Methylpyridine

Conditions
ConditionsYield
Cs exchanged zeolite at 450℃; Product distribution; investigation of the heterogeneous vapor-phase alkylation of pyridine with methanol over Na+, K+, Rb+, or Cs+ exchanged X- or Y-type zeolite in an atmosphere of nitrogen;A 5.5%
B 6.5%
C 5%
D 22.2%
E 5.3%
F 3.1%
54856-82-5

3-methyl-[1,2,3]triazolo[1,5-a]pyridine

98-09-9

benzenesulfonyl chloride

67-64-1

acetone

A

100-69-6

2-vinylpyridine

B

10445-92-8

2-(1-chloroethyl)pyridine

C

127-63-9

diphenyl sulphone

D

2116-62-3

2-(2-phenylethyl)pyridine

E

882-33-7

diphenyldisulfane

F

103-79-7

1-phenyl-acetone

Conditions
ConditionsYield
for 80h; Mechanism; Heating;A n/a
B 4%
C 6%
D n/a
E 1%
F 3%
110-86-1

pyridine

64-17-5

ethanol

A

100-69-6

2-vinylpyridine

B

108-48-5

2,6-dimethylpyridine

C

536-78-7

3-ethylpyridine

D

100-71-0

2-Ethylpyridine

E

536-75-4

4-Ethylpyridine

Conditions
ConditionsYield
Cs exchanged zeolite at 450℃; Product distribution; investigation of the heterogeneous vapor-phase alkylation of pyridine with ethanol over Na+, K+, Rb+, or Cs+ exchanged X- or Y-type zeolite in an atmosphere of nitrogen;A 1.3%
B 1.1%
C 1.1%
D 5.9%
E 3.2%
931-19-1

2-methylpyridine N-oxide

A

110-86-1

pyridine

B

100-69-6

2-vinylpyridine

C

109-06-8

α-picoline

D

4916-40-9

1,2-bis(pyridin-2-yl)ethane

Conditions
ConditionsYield
at 800℃; under 1 - 5 Torr;A n/a
B 5%
C n/a
D n/a
109-06-8

α-picoline

50-00-0

formaldehyd

A

100-69-6

2-vinylpyridine

B

100-71-0

2-Ethylpyridine

Conditions
ConditionsYield
With water at 275℃; beim Leiten ueber mit Zinkfluorid impraegniertes Al2O3;
K-ZSM-5 at 300℃; Conversion of starting material;
109-06-8

α-picoline

50-00-0

formaldehyd

A

100-69-6

2-vinylpyridine

B

103-74-2

2-(2-Hydroxyethyl)pyridine

Conditions
ConditionsYield
With sulfuric acid; water; hydrogen at 160℃;
100-71-0

2-Ethylpyridine

100-69-6

2-vinylpyridine

Conditions
ConditionsYield
With chromium(III) oxide; iron(III) oxide; potassium hydroxide at 700℃; mit Wasserdampf;
With nitrogen; iodine; oxygen at 700℃; beim Leiten ueber Quarz;
With binary vanadium-magnesium catalyst; water; oxygen at 480℃; Product distribution; oxidative dehydrogenation; other alkylpyridines, also in the presence sulfur dioxide, variously modified catalysts, var. temp.;
109-04-6

2-bromo-pyridine

754-05-2

ethenyltrimethylsilane

A

100-69-6

2-vinylpyridine

B

2857-97-8

trimethylsilyl bromide

C

107-46-0

Hexamethyldisiloxane

D

106-99-0

buta-1,3-diene

Conditions
ConditionsYield
bis(η3-allyl-μ-chloropalladium(II)) In tetralin; water; N,N-dimethyl-formamide at 100℃; for 5h; other catalysts: (Ph3P)4Pd, LiPdCl3, (PhCN)2PdCl2, (MeCN)2PdCl2, Pd/C; Et3N presence; Further byproducts given;A 30 % Chromat.
B n/a
C n/a
D n/a
5029-67-4

2-iodopyridine

754-05-2

ethenyltrimethylsilane

A

100-69-6

2-vinylpyridine

B

16029-98-4

trimethylsilyl iodide

C

107-46-0

Hexamethyldisiloxane

D

106-99-0

buta-1,3-diene

Conditions
ConditionsYield
bis(η3-allyl-μ-chloropalladium(II)) In tetralin; water; N,N-dimethyl-formamide at 100℃; for 5h; other catalysts: (Ph3P)4Pd, LiPdCl3, (PhCN)2PdCl2, (MeCN)2PdCl2, Pd/C; Et3N presence; Further byproducts given;A 23 % Chromat.
B n/a
C n/a
D n/a
931-19-1

2-methylpyridine N-oxide

A

110-86-1

pyridine

B

100-69-6

2-vinylpyridine

C

109-06-8

α-picoline

D

1132-37-2

bis(2-pyridyl)methane

E

4916-40-9

1,2-bis(pyridin-2-yl)ethane

Conditions
ConditionsYield
at 550 - 800℃; Product distribution; flash vacuum pyrolysis;
931-19-1

2-methylpyridine N-oxide

A

100-69-6

2-vinylpyridine

B

100-71-0

2-Ethylpyridine

C

586-98-1

2-Hydroxymethylpyridine

D

1132-37-2

bis(2-pyridyl)methane

E

4916-40-9

1,2-bis(pyridin-2-yl)ethane

F

1437-15-6

1,2-bis(2-pyridyl)ethylene

Conditions
ConditionsYield
at 500 - 800℃; under 0.01 - 0.1 Torr; Product distribution; other pyridine and pyridazine N-oxides;
107-13-1

acrylonitrile

74-86-2

acetylene

A

100-69-6

2-vinylpyridine

B

71-43-2

benzene

Conditions
ConditionsYield
With η6-borinato cobalt complexes at 120 - 160℃; under 37503 Torr; Product distribution;
110232-64-9

2-[2-([1,3,2]Dioxaphospholan-2-yloxy)-ethyl]-pyridine

100-69-6

2-vinylpyridine

Conditions
ConditionsYield
at 800℃;
at 700℃; under 0.001 Torr;
31656-92-5

1-azido-2-methyl-benzene

A

100-69-6

2-vinylpyridine

B

16118-22-2

benzylidenamine

C

64372-87-8

6-Methylene-2,4-cyclohexadien-1-imine

D

100-47-0

benzonitrile

Conditions
ConditionsYield
at 800℃;
100-69-6

2-vinylpyridine

108-98-5

thiophenol

21070-71-3

phenyl 2-(2-pyridyl)ethyl sulfide

Conditions
ConditionsYield
at 60℃; for 2.5h; Alkylation;100%
With zinc(II) nitrate hexahydrate In acetonitrile at 25℃; for 0.166667h; Sealed tube; Green chemistry;92%
In water at 20℃;84%
With benzene
unter Zusatz von wenig wss. Benzyl-trimethyl-ammonium-hydroxid-Loesung auf 100grad;
100-69-6

2-vinylpyridine

100-71-0

2-Ethylpyridine

Conditions
ConditionsYield
With 5% Pd/C; hydrogen In ethanol at 20℃; for 0.5h; chemoselective reaction;100%
With 6C53H32O8(4-)*13Zr(4+)*18O(2-)*8Co(2+)*8H(1-); hydrogen In tetrahydrofuran at 20℃; under 30003 Torr; for 36h; Catalytic behavior;99%
With cobalt In tetrahydrofuran Heating; High pressure; chemoselective reaction;99%
100-69-6

2-vinylpyridine

956472-60-9

2-(4′-vinylbiphenyl-4-yl)pyridine

poly(2-(4'-vinylbiphenyl-4-yl)pyridine-co-2-vinylpyridine)

poly(2-(4'-vinylbiphenyl-4-yl)pyridine-co-2-vinylpyridine)

Conditions
ConditionsYield
Stage #1: 2-vinylpyridine With (diphenylmethyl)potassium
Stage #2: 2-(4′-vinylbiphenyl-4-yl)pyridine at -78℃;
100%
100-69-6

2-vinylpyridine

tris(pentafluorophenyl)aluminum*(toluene)0.5

1632067-27-6

(2-vinylpyridine)Al(C6F5)3

Conditions
ConditionsYield
In toluene at 25℃;100%
100-69-6

2-vinylpyridine

5747-23-9

2-phenyl-1,3,2-benzodioxaborole

100-71-0

2-Ethylpyridine

Conditions
ConditionsYield
With oxygen; hydrazine hydrate In acetonitrile at 32℃; under 760.051 Torr; for 3h; Schlenk technique;100%
100-69-6

2-vinylpyridine

75-15-0

carbon disulfide

109-73-9

N-butylamine

2-(pyridin-2-yl)ethyl butylcarbamodithioate

Conditions
ConditionsYield
In neat (no solvent) at 20℃; for 6h; Green chemistry; regioselective reaction;100%
100-69-6

2-vinylpyridine

75-15-0

carbon disulfide

124-02-7

diallylamine

2-(pyridin-2-yl)ethyl diallylcarbamodithioate

Conditions
ConditionsYield
In neat (no solvent) at 20℃; for 6h; Green chemistry; regioselective reaction;100%
100-69-6

2-vinylpyridine

75-15-0

carbon disulfide

156-87-6

propan-1-ol-3-amine

2-(pyridin-2-yl)ethyl 3-hydroxypropylcarbamodithioate

Conditions
ConditionsYield
In neat (no solvent) at 20℃; for 6h; Green chemistry; regioselective reaction;100%
100-69-6

2-vinylpyridine

75-15-0

carbon disulfide

2393-23-9

4-methoxy-benzylamine

2-(pyridin-2-yl)ethyl 4-methoxybenzylcarbamodithioate

Conditions
ConditionsYield
In neat (no solvent) at 20℃; for 6h; Green chemistry; regioselective reaction;100%
100-69-6

2-vinylpyridine

75-15-0

carbon disulfide

3886-69-9

(R)-1-phenyl-ethyl-amine

2-(pyridin-2-yl)ethyl (R)-1-phenylethylcarbamodithioate

Conditions
ConditionsYield
In neat (no solvent) at 20℃; for 6h; Green chemistry; regioselective reaction;100%
100-69-6

2-vinylpyridine

75-15-0

carbon disulfide

109-89-7

diethylamine

2-(pyridin-2-yl)ethyl diethylcarbamodithioate

Conditions
ConditionsYield
In neat (no solvent) at 20℃; for 6h; Green chemistry; regioselective reaction;100%
110-89-4

piperidine

100-69-6

2-vinylpyridine

75-15-0

carbon disulfide

2-(pyridin-2-yl)ethyl piperidine-1-carbodithioate

Conditions
ConditionsYield
In neat (no solvent) at 20℃; for 6h; Green chemistry; regioselective reaction;100%
123-75-1

pyrrolidine

100-69-6

2-vinylpyridine

75-15-0

carbon disulfide

2-(pyridin-2-yl)ethyl pyrrolidine-1-carbodithioate

Conditions
ConditionsYield
In neat (no solvent) at 20℃; for 6h; Green chemistry; regioselective reaction;100%
100-69-6

2-vinylpyridine

75-15-0

carbon disulfide

107-11-9

1-amino-2-propene

2-(pyridin-2-yl)ethyl allylcarbamodithioate

Conditions
ConditionsYield
In neat (no solvent) at 20℃; for 6h; Green chemistry; regioselective reaction;100%
100-69-6

2-vinylpyridine

75-15-0

carbon disulfide

75-04-7

ethylamine

2-(pyridin-2-yl)ethyl ethylcarbamodithioate

Conditions
ConditionsYield
In neat (no solvent) at 20℃; for 6h; Green chemistry; regioselective reaction;100%
100-69-6

2-vinylpyridine

75-15-0

carbon disulfide

75-31-0

isopropylamine

2-(pyridin-2-yl)ethyl isopropylcarbamodithioate

Conditions
ConditionsYield
In neat (no solvent) at 20℃; for 6h; Green chemistry; regioselective reaction;100%
100-69-6

2-vinylpyridine

75-15-0

carbon disulfide

78-81-9

isobutylamine

2-(pyridin-2-yl)ethyl isobutylcarbamodithioate

Conditions
ConditionsYield
In neat (no solvent) at 20℃; for 6h; Green chemistry; regioselective reaction;100%
100-69-6

2-vinylpyridine

696-62-8

para-iodoanisole

19036-99-8

2-(4-Methoxy-styryl)-pyridin

Conditions
ConditionsYield
With potassium phosphate; sodium chloride In water; N,N-dimethyl-formamide at 45℃; for 16h; Catalytic behavior; Reagent/catalyst; Micellar solution;99%
With potassium carbonate; palladium on activated charcoal In N,N-dimethyl-formamide at 100℃;44%
100-69-6

2-vinylpyridine

Reaxys ID: 15741156

Reaxys ID: 15741156

Conditions
ConditionsYield
With ethyl 2-methyl-2-methyl tellurium propionate; 2,2'-azobis(isobutyronitrile) at 60℃; for 3h; Product distribution / selectivity;99%
100-69-6

2-vinylpyridine

626-55-1

3-Bromopyridine

13362-75-9

trans-1-(2-pyridyl)-2-(3-pyridyl)ethylene

Conditions
ConditionsYield
With dicyclohexyl(2',4',6'-triisopropyl-[1,1':3',1''-terphenyl]-2-yl)phosphane; palladium diacetate; sodium hydrogencarbonate In N,N-dimethyl-formamide at 120℃; for 8h; Sealed tube; Inert atmosphere; Glovebox; Schlenk technique;99%
With monophosphine 1,2,3,4,5-pentaphenyl-1'-(di-tert-butylphosphino)ferrocene; palladium diacetate; sodium hydrogencarbonate In N,N-dimethyl-formamide at 120℃; for 4h; Reagent/catalyst; Heck Reaction; Inert atmosphere;99%
With C18H21N3O2Pd; tetrabutylammomium bromide; caesium carbonate In N,N-dimethyl acetamide at 150℃; for 15h; Heck Reaction; Sealed tube;60%
100-69-6

2-vinylpyridine

(E)-1-(pyridin-2-yl)-N-(4-styrylbenzyl)methanamine

(E)-2-(pyridin-2-yl)-N-(pyridin-2-ylmethyl)-N-(4-styrylbenzyl)-ethanamine

Conditions
ConditionsYield
With acetic acid In ethanol for 36h; Reflux;99%
100-69-6

2-vinylpyridine

23516-84-9

2,2,2-trifluoro-1-(4-iodophenyl)ethan-1-one

1,1,1-trifluoro-2-(4-iodophenyl)-4-(pyridin-2-yl)butan-2-ol

Conditions
ConditionsYield
With diphenyl hydrogen phosphate; diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate In dichloromethane at 20℃; Irradiation; Inert atmosphere;99%
100-69-6

2-vinylpyridine

4559-70-0

Diphenylphosphine oxide

25898-97-9

α-<2-(diphenylphosphinyl)ethyl>pyridine

Conditions
ConditionsYield
With pyridine; lanthanum tris(N,N-dimethylbenzylamine) at 80℃; for 16h; Glovebox; regioselective reaction;98%
at 120℃; for 1h; microwave irradiation;88%
With silver fluoride In N,N-dimethyl-formamide at 110℃; for 24h;80%
In benzene at 140℃; for 3.5h;78%
With oxygen at 80℃; for 12h;95 % Spectr.
100-69-6

2-vinylpyridine

696-63-9

4-Methoxybenzenethiol

4-methoxyphenyl 2-(2-pyridyl)ethyl sulfide

Conditions
ConditionsYield
at 60℃; for 2.5h; Alkylation;98%
100-69-6

2-vinylpyridine

106-54-7

p-Chlorothiophenol

2-(2-((4-chlorophenyl)thio)ethyl)pyridine

Conditions
ConditionsYield
In neat (no solvent) at 40℃; for 0.5h;98%
at 60℃; for 2.5h; Alkylation;93%
100-69-6

2-vinylpyridine

75-15-0

carbon disulfide

100-46-9

benzylamine

21172-92-9

2-(pyridin-2-yl)ethyl benzylcarbamodithioate

Conditions
ConditionsYield
In neat (no solvent) at 20℃; for 6h; Green chemistry; regioselective reaction;98%
100-69-6

2-vinylpyridine

C17H16BN2(1+)*C24BF20(1-)

C24H23BN3(1+)*C24BF20(1-)

Conditions
ConditionsYield
In chloroform Inert atmosphere; Schlenk technique;98%
100-69-6

2-vinylpyridine

254454-54-1

tert-butyl-3-iodoazetidine-1-carboxylate

tert-butyl 3-(2-(pyridin-2-yl)ethyl)azetidine-1-carboxylate

Conditions
ConditionsYield
With triethylamine In water; acetonitrile at 20℃; for 16h; Irradiation; chemoselective reaction;98%
123-75-1

pyrrolidine

100-69-6

2-vinylpyridine

6311-90-6

2-[2-(pyrrolidin-1-yl)ethyl]pyridine

Conditions
ConditionsYield
With (dpp-BIAN)Mg(THF)3 In benzene-d6 at 20℃; for 4.1h; Reagent/catalyst; Time; Inert atmosphere; Schlenk technique;97%
With NPs-Fe3O4-DE-bmim3PW In dichloromethane at 20℃; for 2h;90%
With ferrocene; C42H48N2Si2Y(1-)*C16H32LiO4(1+) In benzene-d6 at 130℃; for 0.08h; Inert atmosphere; Glovebox;84%
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    Min.Order: 1 Kilogram

    FOB Price:  USD $ 3.0-3.0/Kilogram

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    Business Type:Lab/Research institutions

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    100-69-6

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    Address:No.200 Zhenhua Rd.Xihu Industrial Park, Hangzhou 310030, China

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    100-69-6

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    100-69-6

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    Siwei Development Group Ltd. is a reputed professional enterprise in China dedicated to the Amino Acids production and sales of fine chemical products.Over the years we have been m

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    100-69-6

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    100-69-6

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    100-69-6

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    Min.Order: 1 Gram

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    100-69-6

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    Business Type:Manufacturers

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    The company is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds,

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    Business Type:Lab/Research institutions

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    Address:32 Room, 5th Floor, Building 11, No. 6 Yinxing Road, High-tech Industrial Development Zone, Zhengzhou City, Henan Province

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    100-69-6

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     China (Mainland)  |  Contact Details

    Business Type:Lab/Research institutions

    Tel:18917157435

    Address:No. 3377, Kang Xin Road, Pudong New Area, Shanghai

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  • Casno:

    100-69-6

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    Min.Order: 1 Kilogram

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    Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard

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  • 2-vinylpyridine

  • Casno:

    100-69-6

    2-vinylpyridine

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Reported in EPA TSCA Inventory.

Specification

The 2-Vinylpyridine, with the CAS registry number 100-69-6, is also known as 2VP. It belongs to the product categories of Pyridines Derivates; Monomers; Polymer Science; Vinyl Halides, Amines, Amides, and Other Vinyl Monomers; C7 and C8; Heterocyclic Building Blocks; Pyridines. Its EINECS registry number is 202-879-8. This chemical's molecular formula is C7H7N and molecular weight is 105.13718. Its IUPAC name is called 2-ethenylpyridine. The product can be used to prepare modification latex of vinyl pyridine with butadiene or styrene copolymerization. In addition, it also can be used for binder. 2-Vinylpyridine is a useful intermediate for the production of polymers.

Physical properties of 2-Vinylpyridine: (1)ACD/LogP: 1.34; (2)ACD/LogD (pH 5.5): 1.23; (3)ACD/LogD (pH 7.4): 1.34; (4)ACD/BCF (pH 5.5): 4.78; (5)ACD/BCF (pH 7.4): 6.1; (6)ACD/KOC (pH 5.5): 99.31; (7)ACD/KOC (pH 7.4): 126.9; (8)#H bond acceptors: 1; (9)#Freely Rotating Bonds: 1; (10)Index of Refraction: 1.562; (11)Molar Refractivity: 35.26 cm3; (12)Molar Volume: 108.6 cm3; (13)Surface Tension: 36.1 dyne/cm; (14)Density: 0.968 g/cm3; (15)Flash Point: 46.7 °C; (16)Enthalpy of Vaporization: 38.05 kJ/mol; (17)Boiling Point: 160.3 °C at 760 mmHg; (18)Vapour Pressure: 3.13 mmHg at 25°C.

Preparation of 2-Vinylpyridine: this chemical can be obtained from 2-hydroxyethyl pyridine by dehydration.

2-Vinylpyridine can be obtained from 2-hydroxyethyl pyridine by dehydration

Uses of 2-Vinylpyridine: it can be used to produce 4-chlorophenyl 2-(2-pyridyl)ethyl sulfide at temperature of 60 °C. This reaction is a kind of Alkylation. It will need 2.5 hours. The yield is about 93%.

2-Vinylpyridine can be used to produce 4-chlorophenyl 2-(2-pyridyl)ethyl sulfide

When you are using this chemical, please be cautious about it as the following:
This chemical may destroy living tissue on contact and may cause burns. In case of contact with eyes, you should rinse immediately with plenty of water and seek medical advice. Whenever you will contact it, please wear suitable protective clothing, gloves and eye/face protection.

You can still convert the following datas into molecular structure:
(1)Canonical SMILES: C=CC1=CC=CC=N1
(2)InChI: InChI=1S/C7H7N/c1-2-7-5-3-4-6-8-7/h2-6H,1H2
(3)InChIKey: KGIGUEBEKRSTEW-UHFFFAOYSA-N

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
guinea pig LDLo skin 500mg/kg (500mg/kg)   "Prehled Prumyslove Toxikologie; Organicke Latky," Marhold, J., Prague, Czechoslovakia, Avicenum, 1986Vol. -, Pg. 845, 1986.
mammal (species unspecified) LD50 oral 415mg/kg (415mg/kg)   Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 39(4), Pg. 86, 1974.
mouse LC50 inhalation 460mg/m3 (460mg/m3)   Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 10(3), Pg. 9, 1966.
mouse LD50 oral 420mg/kg (420mg/kg)   Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 10(3), Pg. 9, 1966.
rat LC50 inhalation 610mg/m3 (610mg/m3)   Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 57(9-10), Pg. 64, 1992.
rat LD50 oral 100mg/kg (100mg/kg)   "Prehled Prumyslove Toxikologie; Organicke Latky," Marhold, J., Prague, Czechoslovakia, Avicenum, 1986Vol. -, Pg. 845, 1986.