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ChemicalBook >> CAS DataBase List >>6-Chloro-2-methyl-3-nitropyridine

6-Chloro-2-methyl-3-nitropyridine

CAS No.
22280-60-0
Chemical Name:
6-Chloro-2-methyl-3-nitropyridine
Synonyms
2-CHLORO-6-METHYL-3-NITROPYRIDINE;2-CHLORO-5-NITRO-6-METHYLPYRIDINE;TIMTEC-BB SBB003830;TIMTEC-BB SBB003832;2-CHLORO-5-NITRO-6-PICOLINE;6-CHLORO-3-NITRO-2-PICOLINE;6-Chloro-2-Methyl-3-nitro...;2-CHLORO-6-METHYL-5-NITROPYRI;6-Chloro-2-methyl-3-nitropyrid;6-Chloro-3-nitro-2-picoline,98%
CBNumber:
CB6466200
Molecular Formula:
C6H5ClN2O2
Molecular Weight:
172.57
MDL Number:
MFCD00234160
MOL File:
22280-60-0.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 02:57:31
Product description Number Pack Size Price
6-Chloro-2-methyl-3-nitropyridine >98.0%(GC) C2434 1g $30
6-Chloro-2-methyl-3-nitropyridine >98.0%(GC) C2434 5g $62
6-Chloro-2-methyl-3-nitropyridine Asreported 270286 10g $232
6-Chloro-2-methyl-3-nitropyridine Asreported 270286 25g $343
2-CHLORO-5-NITRO-6-METHYLPYRIDINE 97% 57634 25G $45
More product size

6-Chloro-2-methyl-3-nitropyridine Properties

Melting point 54-58 °C
Boiling point 200°C (rough estimate)
Density 1.5610 (rough estimate)
refractive index 1.5500 (estimate)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form Powder
pka -3.26±0.10(Predicted)
color Light beige to brown
InChI InChI=1S/C6H5ClN2O2/c1-4-5(9(10)11)2-3-6(7)8-4/h2-3H,1H3
InChIKey GHSRMSJVYMITDX-UHFFFAOYSA-N
SMILES C1(C)=NC(Cl)=CC=C1[N+]([O-])=O
CAS DataBase Reference 22280-60-0(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)Skull and Crossbones (GHS06)
GHS07,GHS06
Signal word  Warning
Hazard statements  H315-H319-H301-H335
Precautionary statements  P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P261-P280a-P301+P310a-P305+P351+P338-P405-P501a
Hazard Codes  Xn,Xi
Risk Statements  36/37/38-20/21/22-22
Safety Statements  36/37/39-26
Hazard Note  Harmful
HazardClass  IRRITANT
HS Code  29333990
NFPA 704
1
2 0

6-Chloro-2-methyl-3-nitropyridine price More Price(76)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical C2434 6-Chloro-2-methyl-3-nitropyridine >98.0%(GC) 22280-60-0 1g $30 2026-04-30 Buy
TCI Chemical C2434 6-Chloro-2-methyl-3-nitropyridine >98.0%(GC) 22280-60-0 5g $62 2026-04-30 Buy
Usbiological 270286 6-Chloro-2-methyl-3-nitropyridine Asreported 22280-60-0 10g $232 2026-06-03 Buy
Usbiological 270286 6-Chloro-2-methyl-3-nitropyridine Asreported 22280-60-0 25g $343 2026-06-03 Buy
AstaTech 57634 2-CHLORO-5-NITRO-6-METHYLPYRIDINE 97% 22280-60-0 25G $45 2026-04-30 Buy
Product number Packaging Price Buy
C2434 1g $30 Buy
C2434 5g $62 Buy
270286 10g $232 Buy
270286 25g $343 Buy
57634 25G $45 Buy

6-Chloro-2-methyl-3-nitropyridine Chemical Properties,Uses,Production

Chemical Properties

Light yellow Cryst

Uses

6-Chloro-2-methyl-3-nitropyridine has been used as a reactant for the synthesis of fluorine-containing pyridinealdoxime derivatives as treatment of organophosphorus nerve-agent poisoning.

Preparation

A mixture of 2-oxo-5-nitro-6-methyl-1,2-dihydropyridine, phosphorous oxychloride, and phosphorous pentachloride was heated at 110° C for 2 hours, whereupon the reaction mixture was charged with an additional portion of phosphorous pentachloride and phosphorous oxychloride. The reaction was stirred for 1 hour and then poured into ice water. The brown solid was filtered and washed with cold water, to give 6-Chloro-2-methyl-3-nitropyridine (94%).
6-Chloro-2-methyl-3-nitropyridine

Synthesis

2-Hydroxy-6-methyl-5-nitropyridine

28489-45-4

6-Chloro-2-methyl-3-nitropyridine

22280-60-0

General procedure for the synthesis of 2-chloro-5-nitro-6-methylpyridine from 2-hydroxy-6-methyl-5-nitropyridine: 1. 2-Hydroxy-6-methyl-5-nitropyridine (500 mg, 3.24 mmol), phosphorus trichloride (POCl3, 0.5 mL) and phosphorus pentachloride (PCl5, 200 mg) were mixed and the reaction was stirred for 2 hours at 150 °C. After completion of the reaction, it was cooled to room temperature, the reaction mixture was poured into ice water and extracted with dichloromethane (DCM, 3 x 20 mL). The organic phases were combined, washed with water to pH 7, dried over anhydrous sodium sulfate (Na2SO4) and concentrated under reduced pressure. The resulting residue was dried under reduced pressure to give 6-chloro-2-methyl-3-nitropyridine (430 mg, 78% yield) as a light brown solid. 2. 3-Ethynyl-7,7-dimethyl-7,8-dihydroquinolin-5(6H)-one (199 mg, 1.00 mmol) was mixed with 6-chloro-2-methyl-3-nitropyridine (172 mg, 1.00 mmol) in the presence of PdCl2(PPh3)2 (42 mg, 0.06 mmol), P(t-Bu)3 (16 mg , 0.08 mmol) and triethylamine (TEA, 1.5 mL) in a solution of N,N-dimethylformamide (DMF, 3 mL), and the reaction was stirred at 100 °C for 3 hours. The crude product was purified by silica gel column chromatography to afford the intermediate 7,7-dimethyl-3-((6-methyl-5-nitropyridin-2-yl)ethynyl)-7,8-dihydroquinolin-5(6H)-one (80 mg, 16% yield) as a yellow solid. 3. 7,7-Dimethyl-3-((6-methyl-5-nitropyridin-2-yl)ethynyl)-7,8-dihydroquinolin-5(6H)-one (194 mg, 0.58 mmol) was dissolved in ethyl acetate (EtOAc, 10 mL) and cooled to 0°C. A concentrated aqueous hydrochloric acid solution (1 mL) of stannous chloride dihydrate (SnCl2-2H2O, 650 mg, 2.90 mmol) was slowly added. The reaction mixture was stirred at room temperature for 3 h. The reaction mixture was poured into ice water, adjusted to pH 9-10 with 15% aqueous sodium hydroxide and extracted with ethyl acetate (EtOAc, 3 × 25 mL). The organic phases were combined, dried over anhydrous sodium sulfate (Na2SO4) and concentrated under reduced pressure. The resulting residue was purified by preparative thin layer chromatography (silica gel, dichloromethane/ethanol, 40:1) to afford the target product 2-chloro-5-nitro-6-methylpyridine (34 mg, 19% yield). Product characterization: 1H NMR (DMSO-d6) δH: 1.05 (s, 6H), 2.29 (s, 3H), 2.59 (s, 2H), 3.03 (s, 2H), 5.51 (br s, 2H), 6.92 (d, 1H), 7.24 (d, 1H), 8.15 (s, 1H), 8.83 (s, 1H). LC/MS (M+H)+ = 306.

References

[1] Journal of Fluorine Chemistry, 2011, vol. 132, # 8, p. 541 - 547
[2] Patent: WO2012/52451, 2012, A1. Location in patent: Page/Page column 113
[3] Patent: CN105906621, 2016, A. Location in patent: Paragraph 0021
[4] Patent: WO2005/42464, 2005, A1. Location in patent: Page/Page column 33
[5] Journal of the American Chemical Society, 1952, vol. 74, p. 3828,3830

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View Lastest Price from 6-Chloro-2-methyl-3-nitropyridine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
6-Chloro-2-methyl-3-nitropyridine pictures 2026-03-20 6-Chloro-2-methyl-3-nitropyridine
22280-60-0
$10.00 1KG 99% 10 mt Hebei Chuanghai Biotechnology Co., Ltd
6-Chloro-2-methyl-3-nitropyridine pictures 2026-02-02 6-Chloro-2-methyl-3-nitropyridine
22280-60-0
$1.00 1g 98% 50tons Shaanxi Dideu Medichem Co. Ltd
6-Chloro-2-methyl-3-nitropyridine pictures 2025-12-01 6-Chloro-2-methyl-3-nitropyridine
22280-60-0
1KG 98.0% 10000KGS Shaanxi Dideu New Materials Co. Ltd

6-Chloro-2-methyl-3-nitropyridine Spectrum

TIMTEC-BB SBB003832 TIMTEC-BB SBB003830 2-CHLORO-6-METHYL-5-NITROPYRIDINE 2-CHLORO-5-NITRO-6-PICOLINE 6-CHLORO-3-NITRO-2-METHYLPYRIDINE 6-CHLORO-3-NITRO-2-PICOLINE 6-CHLORO-2-METHYL-3-NITROPYRIDINE 2-CHLORO-5-NITRO-6-PICOLINE (2-CHLORO-6-METHYL-5-NITROPYRIDINE) 2-Chloro-5-Nitro-6-methylpyrdine 6-Chloro-2-methyl-3-nitro-pyridine ,97% 6-Chloro-3-nitro-2-picoline,98% 6-Chloro-2-methyl-3-nitropyrid 6-Chloro-2-Methyl-3-nitro... Pyridine, 6-chloro-2-methyl-3-nitro- 2-CHLORO-6-METHYL-5-NITROPYRI 6-Chloro-2-methyl-3-nitropyridine > 6-Chloro-2-methyl-3-nitropyridine ISO 9001:2015 REACH 2-CHLORO-6-METHYL-3-NITROPYRIDINE 2-CHLORO-5-NITRO-6-METHYLPYRIDINE 22280-60-0 Pyridine compounds of pyridine Heterocycle-Pyridine series pyridine series Chlorinated heterocyclic series Boronic Acid Pyridines
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