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ChemicalBook >> CAS DataBase List >>2-METHYL-5-NITRO-2H-INDAZOLE

2-METHYL-5-NITRO-2H-INDAZOLE

CAS No.
5228-48-8
Chemical Name:
2-METHYL-5-NITRO-2H-INDAZOLE
Synonyms
Methylnitroindazole;2-methyl-5-nitroindazole;2-methyl-5-nitro-indazole;2-METHYL-5-NITRO-2H-INDAZOLE;2-Methyl-5-nitro-1H-indazole;2H-Indazole, 2-methyl-5-nitro-;2-Methyl-5-nitro-2H-indazole, 98+%;2H-Benzopyrazole, 2-methyl-5-nitro-
CBNumber:
CB8375377
Molecular Formula:
C8H7N3O2
Molecular Weight:
177.16
MDL Number:
MFCD00051809
MOL File:
5228-48-8.mol
MSDS File:
SDS
Last updated:2025-07-24 18:13:52

2-METHYL-5-NITRO-2H-INDAZOLE Properties

Melting point 129-131°C
storage temp. Sealed in dry,Room Temperature
form powder
color Yellow
BRN 167044
FDA UNII H3B9KJ36AQ
UNSPSC Code 12352200

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
Hazard Codes  Xi
HazardClass  IRRITANT
HS Code  2933998090
NFPA 704
1
0 0

2-METHYL-5-NITRO-2H-INDAZOLE price More Price(15)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC M339265 2-Methyl-5-nitro-2H-indazole 5228-48-8 50mg $60 2021-12-16 Buy
SynQuest Laboratories 4H54-1-V6 2-Methyl-5-nitro-2H-indazole 5228-48-8 5G $138 2021-12-16 Buy
Matrix Scientific 042645 2-Methyl-5-nitro-2H-indazole >95% 5228-48-8 500mg $599 2021-12-16 Buy
Matrix Scientific 042645 2-Methyl-5-nitro-2H-indazole >95% 5228-48-8 1g $756 2021-12-16 Buy
AK Scientific W6705 2-Methyl-5-nitro-2H-indazole 5228-48-8 1g $104 2021-12-16 Buy
Product number Packaging Price Buy
M339265 50mg $60 Buy
4H54-1-V6 5G $138 Buy
042645 500mg $599 Buy
042645 1g $756 Buy
W6705 1g $104 Buy

2-METHYL-5-NITRO-2H-INDAZOLE Chemical Properties,Uses,Production

Synthesis

5-Nitroindazole

5401-94-5

Iodomethane

74-88-4

2-METHYL-5-NITRO-2H-INDAZOLE

5228-48-8

1-METHYL-5-NITRO-1H-INDAZOLE

5228-49-9

GENERAL METHOD: Cesium carbonate (12.26 mmol) was added to a tetrahydrofuran (THF; 25 mL) solution of 5-nitroindazole (6.13 mmol) cooled at 0 °C. After stirring for 15 min at 0 °C, iodomethane or allyl bromide (6.13 mmol) was added dropwise. The reaction was monitored by thin layer chromatography (TLC) until the starting material disappeared. Subsequently, the reaction mixture was concentrated by evaporation. The crude product was dissolved in ethyl acetate (EtOAc; 50 mL), washed sequentially with water and brine, and dried over anhydrous magnesium sulfate (MgSO?). After removal of the solvent under reduced pressure, the resulting residue was purified by silica gel column chromatography with ethyl acetate/hexane (3:7, v/v) as eluent to afford 1-alkyl-5-nitroindazole and 2-alkyl-5-nitroindazole, respectively.

References

[1] Synthetic Communications, 2015, vol. 45, # 17, p. 2005 - 2013
[2] Tetrahedron, 2008, vol. 64, # 28, p. 6711 - 6723
[3] Patent: US2014/371219, 2014, A1. Location in patent: Paragraph 0659; 0660; 0661
[4] Patent: WO2016/57834, 2016, A1. Location in patent: Paragraph 000406

2-METHYL-5-NITRO-2H-INDAZOLE Preparation Products And Raw materials

2-METHYL-5-NITRO-2H-INDAZOLE Suppliers

Global( 78)Suppliers
Supplier Tel Email Country ProdList Advantage
Jinan Carbotang Biotech Co.,Ltd.
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Alchem Pharmtech,Inc.
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Fuxin Pharmaceutical
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Career Henan Chemica Co
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Dayang Chem (Hangzhou) Co.,Ltd.
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GIHI CHEMICALS CO.,LIMITED
+8618058761490 info@gihichemicals.com China 49983 58
Aceschem Inc.
+1-817863-6948 +1-(817)863-6948 sales@aceschem.com United States 19632 58

2-METHYL-5-NITRO-2H-INDAZOLE Spectrum

2-METHYL-5-NITRO-2H-INDAZOLE Methylnitroindazole 2-Methyl-5-nitro-2H-indazole, 98+% 2-methyl-5-nitroindazole 2-methyl-5-nitro-indazole 2-Methyl-5-nitro-1H-indazole 2H-Benzopyrazole, 2-methyl-5-nitro- 2H-Indazole, 2-methyl-5-nitro- 5228-48-8 5228-48-2 Indazoles