Buy High Grade Chinese Manufacturer Supply 2,6-Dichloropyridine 2402-78-0 with Low Price
- Molecular Formula:C5H3Cl2N
- Molecular Weight:147.992
- Appearance/Colour:White to light yellow solid
- Vapor Pressure:0.349mmHg at 25°C
- Melting Point:83-86 °C(lit.)
- Refractive Index:1.553
- Boiling Point:206 °C at 760 mmHg
- PKA:-3.02±0.10(Predicted)
- Flash Point:97.5 °C
- PSA：12.89000
- Density:1.388 g/cm3
- LogP:2.38840
2,6-Dichloropyridine(Cas 2402-78-0) Usage
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Purification Methods
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It crystallises from EtOH. [Beilstein 20/5 V 416.]
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Consumer Uses
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ECHA has no public registered data indicating whether or in which chemical products the substance might be used. ECHA has no public registered data on the routes by which this substance is most likely to be released to the environment.
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InChI:InChI=1/C5H3Cl2N/c6-4-2-1-3-5(7)8-4/h1-3H
2402-78-0 Relevant articles
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McKendry,Muelder
, p. 87,94 (1978)
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Highly Chemoselective Deoxygenation of N-Heterocyclic N-Oxides Using Hantzsch Esters as Mild Reducing Agents
An, Ju Hyeon,Kim, Kyu Dong,Lee, Jun Hee
supporting information, p. 2876 - 2894 (2021/02/01)
Herein, we disclose a highly chemoselect...
Production method of 2, 6-dichloropyridine
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Paragraph 0027-0060, (2020/05/01)
The invention discloses a production met...
Catalyst-Free N-Deoxygenation by Photoexcitation of Hantzsch Ester
Cardinale, Luana,Jacobi Von Wangelin, Axel,Konev, Mikhail O.
supporting information, (2020/02/15)
A mild and operationally simple protocol...
Method for preparing 2,6-dichloropyridine by pyridine liquid-phase photochlorination
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Paragraph 0016-0027; 0028; 0029; 0031, (2019/01/23)
The invention relates to a method for pr...
2402-78-0 Process route
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- 1073-67-2,24991-47-7
4-vinylbenzyl chloride
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- 2587-00-0
2,6-dichloropyridine N-oxide
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- 2402-78-0
2,6-dichloropyridine
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- 2788-86-5,53649-47-1,97466-49-4,21019-51-2
(R)-2-(4-chlorophenyl)oxirane
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- 2788-86-5,21019-51-2,53649-47-1,97466-49-4
(2S)-2-(4-chlorophenyl)oxirane
Conditions
| Conditions |
Yield |
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chiral ruthenium porphyrin complex catalyst; In toluene; at -10 ℃; for 48h; Title compound not separated from byproducts.;
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- 614-45-9
tert-Butyl peroxybenzoate
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- 626-60-8
3-Chloropyridine
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- 109-09-1
2-chloropyridine
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- 626-61-9
4-Chloropyridine
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- 2402-78-0
2,6-dichloropyridine
Conditions
| Conditions |
Yield |
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pyridine; With chlorine; di-tert-butyl peroxide; In tetrachloromethane; water; at 231 - 244 ℃; for 0.00361111 - 0.00722222h;
tert-Butyl peroxybenzoate; Product distribution / selectivity;
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35% |
2402-78-0 Upstream products
2402-78-0 Downstream products
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45644-21-1
6-chloropyridin-2-amine
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35299-71-9
2,6-bis(thiophen-2-yl)pyridine
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3980-49-2
2,6-di(piperidine-1-yl)pyridine
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19946-28-2
2-chloro-6-(1-piperidyl)pyridine
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