2,3,4,6-Tetrachloropyridine
2,3-dichloro-pyridine
Conditions | Yield |
---|---|
With hydrogen; triethylamine; urea; citric acid In ethyl acetate at 50℃; under 7500.75 Torr; for 7h; Solvent; Temperature; Pressure; Reagent/catalyst; Autoclave; | 98.1% |
Conditions | Yield |
---|---|
With carbonylhydridetris(triphenylphosphine)rhodium(I); hydrogen; triethylamine In methanol at 60℃; under 450045 Torr; Temperature; Solvent; Pressure; Autoclave; | 98% |
With methanol; palladium 10% on activated carbon; 3-p-menthene at 60℃; for 4h; Temperature; Reagent/catalyst; | 95% |
With hydrogen In methanol at 75℃; under 750.075 Torr; for 8h; Reagent/catalyst; Autoclave; | 95.3% |
Conditions | Yield |
---|---|
In dimethyl sulfoxide | A 96.3% B n/a |
Conditions | Yield |
---|---|
Stage #1: 2-chloro-3-aminopyridine With hydrogenchloride; sodium nitrite In water at 5 - 15℃; for 0.75h; Stage #2: With hydrogenchloride; aminosulfonic acid; copper(II) chloride dihydrate In water at 55 - 62℃; Product distribution / selectivity; | 95% |
With hydrogenchloride; thionyl chloride; nitric acid In water at 0 - 5℃; | 91% |
With hydrogenchloride; sodium nitrite In water at -5 - 40℃; for 1h; Sandmeyer Reaction; Cooling with ice; Inert atmosphere; | 83% |
2-hydroxy-3-chloropyridine
2,3-dichloro-pyridine
Conditions | Yield |
---|---|
With phosphorus pentachloride In 1,2-dichloro-ethane at 60 - 65℃; for 10h; Reagent/catalyst; Temperature; Solvent; | 94.9% |
With phosphorus pentachloride In 1,2-dichloro-ethane at 60 - 65℃; for 10h; Reagent/catalyst; Temperature; | 94.9% |
With trichlorophosphate In 1,2-dichloro-ethane; N,N-dimethyl-formamide Reflux; | 43g |
Conditions | Yield |
---|---|
With hydrogenchloride; copper dichloride; sodium nitrite In water at 20 - 45℃; for 5h; Reagent/catalyst; Large scale; | 89.5% |
Conditions | Yield |
---|---|
With trichlorophosphate In N,N-dimethyl-formamide at 0 - 30℃; for 9h; Reagent/catalyst; | 88% |
With chlorine In dichloromethane at 35 - 40℃; for 4h; Solvent; Temperature; | 126 g |
With sulfolane; phosphorus pentachloride; trichlorophosphate at 150℃; for 6h; Reagent/catalyst; |
Conditions | Yield |
---|---|
With pyridine; hydrogen In water at 40 - 60℃; under 2250.23 - 3750.38 Torr; Reagent/catalyst; Temperature; Pressure; Large scale; | 86.6% |
With pyridine; hydrogen In water at 40 - 60℃; under 2250.23 - 3750.38 Torr; Temperature; Pressure; Reagent/catalyst; Large scale; | 86.6% |
Conditions | Yield |
---|---|
With Dichlorophenylphosphine In various solvent(s) at 170℃; for 5h; | 81% |
With sulfolane; phosphorus pentachloride; trichlorophosphate at 150℃; for 6h; Reagent/catalyst; |
2,3-dichloro-pyridine
Conditions | Yield |
---|---|
Stage #1: 3-chloro-2-pyridinesulfonic acid With hydrogenchloride; water In water at 103℃; for 5h; Stage #2: With sodium chlorate for 5h; Temperature; Reflux; | 80.3% |
Conditions | Yield |
---|---|
With dichloromethane | 80% |
3-chloropyridine-2-carboxylic acid
2,3-dichloro-pyridine
Conditions | Yield |
---|---|
With tert-butylhypochlorite; dichloromethane; sodium hydrogencarbonate at 60℃; for 20h; Green chemistry; | 80% |
With tert-butylhypochlorite; sodium carbonate; sodium chloride In dichloromethane at 30℃; for 20h; Schlenk technique; | 50% |
2-Ethoxy-3-chloropyridine
2,3-dichloro-pyridine
Conditions | Yield |
---|---|
With N,N-dimethyl-formamide; trichlorophosphate at 95℃; for 12h; | 66% |
2,3-dichloro-pyridine
Conditions | Yield |
---|---|
With N,N-dimethyl-formamide; trichlorophosphate at 95℃; for 12h; | 66% |
Conditions | Yield |
---|---|
With chlorine In cyclohexane at 75℃; for 1h; | A 9% B 62% C 4.5% |
Conditions | Yield |
---|---|
Stage #1: 3-Chloropyridine With n-butyllithium In hexane at -60℃; for 1h; Stage #2: With hexachloroethane In tetrahydrofuran; hexane at -60 - 20℃; | 60% |
Multi-step reaction with 3 steps 1: 3-chloro-benzenecarboperoxoic acid / chloroform / 20 °C 2: 30 h / Reflux 3: trichlorophosphate / 6 h / 100 °C View Scheme |
2-methoxy,3-chloropyridine
2,3-dichloro-pyridine
Conditions | Yield |
---|---|
With trichlorophosphate In N,N-dimethyl-formamide at 95℃; for 12h; | 59% |
With N,N-dimethyl-formamide; trichlorophosphate at 95℃; for 12h; | 59% |
5,6-dichloronicotinic acid
2,3-dichloro-pyridine
Conditions | Yield |
---|---|
at 150℃; bei vorsichtiger Destillation unter vermindertem Druck; |
3-chloropyridine-N-oxide
A
2,5 dichloropyridine
B
2,3-dichloro-pyridine
C
3,4-dichloropyridine
Conditions | Yield |
---|---|
With trichlorophosphate at 110℃; for 2h; Yield given. Yields of byproduct given; |
2-Chloro-pyridine-3-diazonium; chloride
2,3-dichloro-pyridine
Conditions | Yield |
---|---|
With hydrogenchloride; copper(II) oxide In n-BuCl; water at 55 - 62℃; Product distribution / selectivity; | |
With hydrogenchloride; copper dichloride In n-Butyl chloride; water at 60℃; for 1.5h; Product distribution / selectivity; |
2-chloro-3-aminopyridine
A
2,3-dichloro-pyridine
B
3,3'-dithiobis(2-chloropyridine)
C
2-chloro-3-pyridinesulfonyl chloride
D
2-chloropyridine-3-sulfonic acid
Conditions | Yield |
---|---|
Stage #1: 2-chloro-3-aminopyridine With hydrogenchloride; acetic acid; sodium nitrite In water at 0℃; Sandmeyer reaction; Stage #2: With sulfur dioxide; water; acetic acid; copper(l) chloride at 0℃; Sandmeyer reaction; |
Conditions | Yield |
---|---|
Stage #1: pyridin-3-ylamine With hydrogenchloride; iron(III) chloride; chlorine; sodium nitrite In water at -8 - 20℃; Stage #2: With hydrogenchloride; copper(l) chloride In water at 60 - 70℃; | |
Multi-step reaction with 2 steps 1: iron(III) chloride; hydrogenchloride; chlorine / water / 25 °C 2: iron(III) chloride; sodium nitrite / water / 30 °C View Scheme | |
Stage #1: pyridin-3-ylamine With hydrogenchloride; dihydrogen peroxide In water at 5℃; for 2h; Stage #2: With sodium nitrite In water at -5℃; for 0.416667h; Stage #3: With copper(l) chloride In dichloromethane; water at 15 - 30℃; for 1.33333h; | |
Multi-step reaction with 2 steps 1: dihydrogen peroxide / 1 h / 5 - 15 °C 2: copper(l) chloride; sodium nitrite / water / 0.5 h / 33 - 38 °C View Scheme |
2-Chloronicotinoyl chloride
2,3-dichloro-pyridine
Conditions | Yield |
---|---|
With oxalyl dichloride; palladium 10% on activated carbon In chlorobenzene at 380 - 395℃; for 1h; Time; Reagent/catalyst; Temperature; Solvent; Concentration; Inert atmosphere; | 43 %Spectr. |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: sodium hydroxide; sodium hypochlorite / 2 h / 10 - 95 °C 2: iron(III) chloride; hydrogenchloride; chlorine / water / 25 °C 3: iron(III) chloride; sodium nitrite / water / 30 °C View Scheme | |
Multi-step reaction with 3 steps 1: sodium hypochlorite / water / 2.5 h / 0 - 100 °C 2: dihydrogen peroxide / 1 h / 5 - 15 °C 3: copper(l) chloride; sodium nitrite / water / 0.5 h / 33 - 38 °C View Scheme |
2-acetyloxy-3-chloropyridine
2,3-dichloro-pyridine
Conditions | Yield |
---|---|
With trichlorophosphate at 100℃; for 6h; Reagent/catalyst; |
Conditions | Yield |
---|---|
With dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; hydrogen; triethylamine In isopropyl alcohol at 85℃; under 3750.38 Torr; for 3h; |
Conditions | Yield |
---|---|
With Wilkinson's catalyst; hydrogen; triethylamine In isopropyl alcohol at 85℃; under 3750.38 Torr; for 1h; |
Conditions | Yield |
---|---|
Stage #1: pyridine With iron(III) chloride; chlorine In tetrachloromethane Large scale; Stage #2: With palladium on activated charcoal In tetrachloromethane; ethanol at 80℃; under 750.075 Torr; Reagent/catalyst; Solvent; Pressure; Temperature; Large scale; | A 8 kg B 1840.8 kg |
3-pyridyl acetate
2,3-dichloro-pyridine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: chlorine / dichloromethane; water / 4 h / 20 - 30 °C 2: water / dichloromethane / 2 h / 35 - 40 °C 3: chlorine / dichloromethane / 4 h / 35 - 40 °C View Scheme |
2,3-dichloro-pyridine
bis(triphenylphosphine)nickel(II) chloride
[NiCl(ClC5H3N)(P(C6H5)3)]2
Conditions | Yield |
---|---|
With Zn; azabis(isobutyronitrile) In tetrahydrofuran (Ar); stirring (25°C, 1 h); solvent removal, extracting (CH2Cl2), filtn., solvent removal, stirring (Et2O), filtn., recrystallization (CH2Cl2); elem. anal.; | 99% |
Conditions | Yield |
---|---|
Stage #1: pyrrole With sodium hydride In N,N-dimethyl-formamide at 0 - 20℃; for 0.5h; Stage #2: 2,3-dichloro-pyridine In N,N-dimethyl-formamide at 80℃; for 3h; | 99% |
2,3-dichloro-pyridine
(3-chloro-2-pyridyl)hydrazine
Conditions | Yield |
---|---|
With N-Methyldiethanolamine; hydrazine hydrate at 102 - 105℃; under 2250.23 - 3000.3 Torr; for 8h; Inert atmosphere; Autoclave; Large scale; | 98.12% |
With hydrazine hydrate In ethanol for 25h; Reflux; | 97.6% |
With hydrazine hydrate In ethanol for 25h; Reflux; | 96% |
Conditions | Yield |
---|---|
With copper(l) iodide; potassium phosphate tribasic heptahydrate; palladium diacetate; nixantphos In N,N-dimethyl-formamide at 120℃; for 12h; Inert atmosphere; | 98% |
2,3-dichloro-pyridine
tri(p-tolyl)bismuth
3-chloro-2-(4-methylphenyl)pyridine
Conditions | Yield |
---|---|
With tetrakis(triphenylphosphine) palladium(0); caesium carbonate In N,N-dimethyl acetamide at 90℃; for 4h; Inert atmosphere; Schlenk technique; regioselective reaction; | 97% |
2,3-dichloro-pyridine
2,3-dichloropyridine 1-oxide
Conditions | Yield |
---|---|
With trifluoromethylsulfonic anhydride; urea hydrogen peroxide adduct In dichloromethane at 10 - 20℃; | 96% |
With 3-chloro-benzenecarboperoxoic acid In dichloromethane at 0 - 30℃; for 32h; Inert atmosphere; | 74% |
With dihydrogen peroxide; acetic anhydride 1.)r.t., 5 h 2.)60-65 deg C, 30 h; | |
With urea hydrogen peroxide adduct; trifluoroacetic anhydride In dichloromethane at 0 - 20℃; | 11 g |
Conditions | Yield |
---|---|
Stage #1: 2,3-dichloro-pyridine With n-butyllithium; diisopropylamine In tetrahydrofuran; hexane at -75℃; for 2h; Stage #2: carbon dioxide at -78℃; | 96% |
Stage #1: 2,3-dichloro-pyridine With n-butyllithium; diisopropylamine In tetrahydrofuran; hexane at -78 - -25℃; for 3h; Stage #2: carbon dioxide In tetrahydrofuran; hexane at 20℃; for 18h; Stage #3: With hydrogenchloride; water In tetrahydrofuran; diethyl ether; hexane at 0 - 20℃; | 80% |
2,3-dichloro-pyridine
2,2,3,3-tetrafluoropropanol
3-chloro-2-(2,2,3,3-tetrafluoropropyl)pyridine
Conditions | Yield |
---|---|
Stage #1: 2,2,3,3-tetrafluoropropanol With sodium hydride In tetrahydrofuran; mineral oil at 0 - 20℃; for 1h; Stage #2: 2,3-dichloro-pyridine In tetrahydrofuran; mineral oil for 16h; Reflux; | 96% |
Stage #1: 2,2,3,3-tetrafluoropropanol With sodium hydride In tetrahydrofuran; mineral oil at 0 - 20℃; for 1h; Stage #2: 2,3-dichloro-pyridine In tetrahydrofuran; mineral oil for 16h; Reflux; | 96% |
2,3-dichloro-pyridine
2-(prop-2-yloxycarbonyl)-5-trfluoromethylphenylboronic acid
lithium hydroxide
2-(3-chloro-pyridin-2-yl)-4-trifluoromethyl-benzoic acid
Conditions | Yield |
---|---|
Stage #1: 2,3-dichloro-pyridine; 2-(prop-2-yloxycarbonyl)-5-trfluoromethylphenylboronic acid With tetrakis(triphenylphosphine) palladium(0); sodium carbonate In 1,4-dioxane; water at 30 - 110℃; for 20h; Inert atmosphere; Stage #2: lithium hydroxide In 1,4-dioxane; water at 70℃; | 96% |
2,3-dichloro-pyridine
5-bromo-2-(3-chloro-pyridin-2-yl)-3,4-dihydro-2H-pyrazole-3-carboxylic acid ethyl ester
Conditions | Yield |
---|---|
With sodium ethanolate In ethanol at 83℃; for 3h; | 94.9% |
Conditions | Yield |
---|---|
In butan-1-ol for 3h; Reflux; | 94% |
In butan-1-ol for 18h; Reflux; | 92% |
In ethanol 1.) ice bath, 2.) room temperature; | 90.8% |
2,3-dichloro-pyridine
2-(adamantan-1-yloxy)ethan-1-amine
Conditions | Yield |
---|---|
With 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; bis(dibenzylideneacetone)-palladium(0); sodium t-butanolate In 1,4-dioxane Reagent/catalyst; Solvent; Temperature; Inert atmosphere; Reflux; | 94% |
2-aminopyridine
2,3-dichloro-pyridine
3-chloro-N-(pyridin-2-yl)pyridin-2-amine
Conditions | Yield |
---|---|
With potassium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; palladium diacetate In toluene for 18h; Heating; | 93% |
With palladium diacetate; potassium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In toluene at 180℃; for 0.5h; Buchwald-Hartwig amination; Inert atmosphere; Microwave irradiation; regioselective reaction; | 81% |
With palladium diacetate; triphenylphosphine; sodium t-butanolate In toluene at 120℃; for 17h; Inert atmosphere; | 61.7% |
2,3-dichloro-pyridine
4-methoxy-aniline
3-chloro-N-(4-methoxyphenyl)pyridin-2-amine
Conditions | Yield |
---|---|
With potassium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; palladium diacetate In toluene for 18h; Heating; | 93% |
With palladium diacetate; potassium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In toluene for 18h; Buchwald-Hartwig reaction; Reflux; regioselective reaction; | 93% |
Stage #1: 2,3-dichloro-pyridine With palladium diacetate; triphenylphosphine; sodium t-butanolate In toluene under 20 Torr; for 0.166667h; Buchwald-Hartwig Coupling; Inert atmosphere; Stage #2: 4-methoxy-aniline In toluene at 100℃; for 16h; Buchwald-Hartwig Coupling; Inert atmosphere; | 91% |
With palladium diacetate; potassium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In toluene at 180℃; for 0.5h; Buchwald-Hartwig amination; Inert atmosphere; Microwave irradiation; regioselective reaction; | 82% |
Conditions | Yield |
---|---|
Stage #1: 2,3-dichloro-pyridine With palladium diacetate; triphenylphosphine; sodium t-butanolate In toluene under 20 Torr; for 0.166667h; Buchwald-Hartwig Coupling; Inert atmosphere; Stage #2: 3.5-dimethoxyaniline In toluene at 100℃; for 16h; Buchwald-Hartwig Coupling; Inert atmosphere; | 93% |
Stage #1: 2,3-dichloro-pyridine; 3.5-dimethoxyaniline With palladium diacetate; triphenylphosphine; sodium t-butanolate In o-xylene at 120℃; for 3h; Inert atmosphere; Stage #2: With palladium diacetate; 1,8-diazabicyclo[5.4.0]undec-7-ene; tricyclohexylphosphine tetrafluoroborate In N,N-dimethyl acetamide; o-xylene at 145℃; for 16h; Inert atmosphere; | 66% |
With palladium diacetate; triphenylphosphine; sodium t-butanolate Inert atmosphere; Heating; |
2,3-dichloro-pyridine
sodium 4-methylbenzenesulfinate
3-chloro-2-(toluene-4-sulfonyl)-pyridine
Conditions | Yield |
---|---|
With hydrogenchloride; tetrabutyl-ammonium chloride In N,N-dimethyl acetamide; water at 100℃; for 24h; | 93% |
4-HYDROXYPIPERIDINE
2,3-dichloro-pyridine
1-(3-chloropyridin-2-yl)piperidin-4-ol
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 120℃; | 93% |
In N,N-dimethyl-formamide at 80 - 90℃; for 3h; | 1.76 g |
2,3-dichloro-pyridine
Conditions | Yield |
---|---|
With sodium methylate In methanol at 80℃; for 3h; | 92.7% |
Conditions | Yield |
---|---|
With potassium carbonate In dimethyl sulfoxide at 150℃; for 16h; | 92.5% |
With triethylamine In ethanol at 160℃; | |
With N-ethyl-N,N-diisopropylamine In dimethyl sulfoxide at 125℃; for 12h; |
2,3-dichloro-pyridine
tris(4-methoxyphenyl)bismuth
Conditions | Yield |
---|---|
With tetrakis(triphenylphosphine) palladium(0); caesium carbonate In N,N-dimethyl acetamide at 90℃; for 4h; Inert atmosphere; Schlenk technique; regioselective reaction; | 92% |
Conditions | Yield |
---|---|
With potassium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; palladium diacetate In toluene for 18h; Heating; | 91% |
2,3-dichloro-pyridine
2-methoxy-phenylamine
3-chloro-N-(2-methoxyphenyl)pyridin-2-amine
Conditions | Yield |
---|---|
With palladium diacetate; potassium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In toluene for 18h; Buchwald-Hartwig reaction; Reflux; regioselective reaction; | 91% |
Stage #1: 2,3-dichloro-pyridine With palladium diacetate; triphenylphosphine; sodium t-butanolate In toluene under 20 Torr; for 0.166667h; Buchwald-Hartwig Coupling; Inert atmosphere; Stage #2: 2-methoxy-phenylamine In toluene at 100℃; for 16h; Buchwald-Hartwig Coupling; Inert atmosphere; | 82% |
With potassium carbonate; palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In toluene at 120℃; for 2h; | 81% |
Conditions | Yield |
---|---|
With palladium diacetate; potassium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In toluene at 130℃; for 16h; Inert atmosphere; | 91% |
With palladium diacetate; potassium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In toluene at 130℃; for 16h; Buchwald-Hartwig Coupling; Inert atmosphere; | 91% |
With palladium diacetate; potassium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In toluene at 130℃; for 16h; Inert atmosphere; | 91% |
With palladium diacetate; potassium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In toluene at 130℃; for 16h; Inert atmosphere; | 90% |
With palladium diacetate; potassium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In toluene at 180℃; for 0.5h; Buchwald-Hartwig amination; Inert atmosphere; Microwave irradiation; regioselective reaction; | 52% |
Conditions | Yield |
---|---|
With palladium diacetate; potassium carbonate; nixantphos In tetrahydrofuran; water at 20℃; for 6h; Suzuki-Miyaura Coupling; | 91% |
Conditions | Yield |
---|---|
With tetrakis(triphenylphosphine) palladium(0) In tetrahydrofuran at 70℃; for 18h; Inert atmosphere; | 91% |
Molecular Structure of 2,3-Dichloropyridine (CAS NO.2402-77-9):
IUPAC Name: 2,3-Dichloropyridine
Canonical SMILES: C1=CC(=C(N=C1)Cl)Cl
InChI: InChI=1S/C5H3Cl2N/c6-4-2-1-3-8-5(4)7/h1-3H
InChIKey: MAKFMOSBBNKPMS-UHFFFAOYSA-N
Molecular Weight: 147.99002 [g/mol]
Molecular Formula: C5H3Cl2N
XLogP3: 2.1
H-Bond Donor: 0
H-Bond Acceptor: 1
EINECS: 219-281-8
Index of Refraction: 1.553
Molar Refractivity: 34.13 cm3
Molar Volume: 106.5 cm3
Surface Tension: 43.1 dyne/cm
Density: 1.388 g/cm3
Flash Point: 87.5 °C
Enthalpy of Vaporization: 41.11 kJ/mol
Boiling Point: 192.5 °C at 760 mmHg
Vapour Pressure: 0.679 mmHg at 25 °C
Appearance: White to slightly beige crystalline powder
Melting Point: 64-67 °C(lit.)
Water Solubility: slightly soluble
Product Categories: blocks; Pyridines; Pyridine; Halides; Heterocycles; Pyridines, Pyrimidines, Purines and Pteredines; Pyridine series; Pyridines derivates; Chloropyridines; Halopyridines; Boronic Acid; C5Heterocyclic Building Blocks; Halogenated Heterocycles; Heterocyclic Building Blocks; Chlorinated heterocyclic series
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LD50 | intraperitoneal | 135mg/kg (135mg/kg) | BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) BEHAVIORAL: ANTIPSYCHOTIC LIVER: FATTY LIVER DEGERATION | Toxicology and Applied Pharmacology. Vol. 11, Pg. 361, 1967. |
Safety Information of 2,3-Dichloropyridine (CAS NO.2402-77-9):
Hazard Codes: Xi,Xn
Risk Statements: 36/37/38-22
R36/37/38:Irritating to eyes, respiratory system and skin.
R22:Harmful if swallowed.
Safety Statements: 26-36-37/39
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36:Wear suitable protective clothing.
S37/39:Wear suitable gloves and eye/face protection.
WGK Germany: 3
RTECS: US8050000
Hazard Note: Irritant
HazardClass: IRRITANT
2,3-Dichloropyridine (CAS NO.2402-77-9), its Synonyms are Pyridine, 2,3-dichloro- ; 2,3-Dichlopyridine ; 2,3-Dichloro-pyridine .
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