• Product NameSecnidazole
  • CasNo. 3366-95-8
  • MFC7H11N3O3
  • MW185.183
  • Purity
  • AppearanceCrystalline solid
  • Packing
  • Contact usInquiry

Product Details

CasNo: 3366-95-8

MF: C7H11N3O3

Appearance: Crystalline solid

Manufacturers supply cost-effective and customizable Secnidazole 3366-95-8

  • Molecular Formula:C7H11N3O3
  • Molecular Weight:185.183
  • Appearance/Colour:Crystalline solid 
  • Vapor Pressure:5.49E-07mmHg at 25°C 
  • Melting Point:76 °C 
  • Refractive Index:1.597 
  • Boiling Point:396.1 °C at 760 mmHg 
  • PKA:14.50±0.20(Predicted) 
  • Flash Point:193.4 °C 
  • PSA:83.87000 
  • Density:1.39 g/cm3 
  • LogP:1.00370 

alpha,2-Dimethyl-5-nitro-1H-imidazole-1-ethanol(Cas 3366-95-8) Usage

Pharmaceutical Applications

A 5-nitroimidazole with properties similar to those of metronidazole. It is rapidly absorbed after oral administration and is distinguished by having the longest plasma half-life (18 h) of clinically used nitroimidazole drugs. It is used in the treatment of intestinal amebiasis, giardiasis, trichomoniasis and bacterial vaginosis.

InChI:InChI=1/C7H11N3O3/c1-5(11)4-9-6(2)8-3-7(9)10(12)13/h3,5,11H,4H2,1-2H3

3366-95-8 Relevant articles

Process for preparing 5-nitroimidazole medicine through catalysis of small organic molecules

-

Paragraph 0041-0046; 0051-0052, (2020/08/09)

The invention provides a process for pre...

Synthesis method of 5-nitroimidazole drugs

-

Paragraph 0041; 0042; 0043; 0051; 0052, (2020/04/06)

The invention provides a synthesis metho...

NITRATION

-

Page/Page column 36; 44; 73, (2020/05/28)

The present invention relates to a proce...

Synthetic Secnidazole method and Secnidazole

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Paragraph 0036-0042, (2016/10/07)

The invention discloses a method for syn...

3366-95-8 Process route

2-methyl-5-nitro-1H-imidazole
696-23-1,88054-22-2

2-methyl-5-nitro-1H-imidazole

methyloxirane
75-56-9,16033-71-9

methyloxirane

secnidazole
3366-95-8

secnidazole

Conditions
Conditions Yield
With 1-[3,5-bis(trifluoromethyl)phenyl]-3-[2-(dimethylamino)cyclohexyl]thiourea; In ethyl acetate; at 25 - 30 ℃; for 6h; Solvent; Temperature; Reagent/catalyst;
80.5%
With aluminum (III) chloride; In ethyl acetate; at 45 - 50 ℃; for 1.5h; Temperature;
75%
1-bromo-2-propanol
19686-73-8

1-bromo-2-propanol

2-methyl-5-nitro-1H-imidazole
696-23-1,88054-22-2

2-methyl-5-nitro-1H-imidazole

secnidazole
3366-95-8

secnidazole

Conditions
Conditions Yield
With potassium carbonate; In acetone; at 70 ℃; for 5h; Reagent/catalyst; Temperature;
89.1%

3366-95-8 Upstream products

  • 19686-73-8
    19686-73-8

    1-bromo-2-propanol

  • 696-23-1
    696-23-1

    2-methyl-5-nitro-1H-imidazole

  • 75-56-9
    75-56-9

    methyloxirane

  • 34091-34-4
    34091-34-4

    1-(2-methyl-imidazol-1-yl)-propan-2-ol

3366-95-8 Downstream products

  • 1146349-32-7
    1146349-32-7

    1-[4-(4-fluorobenzenesulfonylmethyl)-2-methyl-5-nitroimidazol-1-yl]propan-2-ol

  • 1326302-64-0
    1326302-64-0

    1-(2-methyl-5-nitro-1H-imidazol-1-yl)propan-2-yl (E)-3-p-tolylacrylate

  • 1326302-58-2
    1326302-58-2

    1-(2-methyl-5-nitro-1H-imidazol-1-yl)propan-2-yl (E)-3-(3-fluorophenyl)acrylate

  • 1326302-55-9
    1326302-55-9

    1-(2-methyl-5-nitro-1H-imidazol-1-yl)propan-2-yl (E)-3-(2-chlorophenyl)acrylate

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