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3,4,5-TRIHYDROXYBENZAMIDE

  • CAS:618-73-5
  • purity:99%
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1.What is the 3,4,5-TRIHYDROXYBENZAMIDE ?

Used in Pharmaceutical Industry:
3,4,5-TRIHYDROXYBENZAMIDE is used as a chelating agent for metal-ion complexation, which is crucial in the production of pharmaceuticals. Its ability to bind with metal ions aids in the development of drugs that require metal ion interaction for their therapeutic effects.
Used in Metal Poisoning Treatment:
In the medical field, 3,4,5-TRIHYDROXYBENZAMIDE is utilized as a chelating agent for the treatment of metal poisoning. Its capacity to form stable complexes with toxic metal ions helps in reducing their harmful effects on the body and facilitates their safe elimination.
Used in Organic Synthesis:
3,4,5-TRIHYDROXYBENZAMIDE serves as a building block in the synthesis of various organic compounds. Its structural features make it a key component in the creation of new molecules with potential applications in different industries.
Used in Antioxidant and Anti-Inflammatory Applications:
3,4,5-TRIHYDROXYBENZAMIDE has demonstrated potential as an antioxidant and anti-inflammatory agent. In the field of medicinal chemistry, it is being explored for its ability to combat oxidative stress and inflammation, which are implicated in various diseases and conditions. Its properties make it a promising candidate for the development of new therapeutic drugs targeting these pathways.

N,N-dimethyl-formamide
68-12-2,33513-42-7

N,N-dimethyl-formamide

p-chloroacetophenone phenylhydrazone
57845-08-6

p-chloroacetophenone phenylhydrazone

1-phenyl-3-(4-chlorophenyl)-4-pyrazolecarboxaldehyde
36663-00-0

1-phenyl-3-(4-chlorophenyl)-4-pyrazolecarboxaldehyde

Conditions
Conditions Yield
With trichlorophosphate; for 11h; Reflux;
90%
With trichlorophosphate;
89.6%
With trichlorophosphate; at 70 - 80 ℃; for 1h;
87%
With trichlorophosphate; for 1h; Cooling; Reflux;
87%
N,N-dimethyl-formamide; With trichlorophosphate; at 0 ℃;
p-chloroacetophenone phenylhydrazone; at 20 ℃; Reflux;
85%
With trichlorophosphate; at 60 ℃; for 6h;
70%
With trichlorophosphate; at 50 - 60 ℃;
With trichlorophosphate; at 50 - 60 ℃;
With trichlorophosphate; Reflux;
With trichlorophosphate;
N,N-dimethyl-formamide; p-chloroacetophenone phenylhydrazone; With trichlorophosphate;
With sodium hydrogencarbonate; In water;
With trichlorophosphate; Inert atmosphere;
With trichlorophosphate;
With trichlorophosphate; at 0 - 80 ℃; for 5h;
With trichlorophosphate; at 90 ℃; for 4h;
N,N-dimethyl-formamide; With trichlorophosphate; at 0 - 5 ℃; for 0.5h;
p-chloroacetophenone phenylhydrazone; In N,N-dimethyl-formamide; at 50 ℃; for 3h;
With trichlorophosphate; at 0 - 90 ℃; for 2h;
With trichlorophosphate; at 50 - 60 ℃; for 6h; Cooling;
p-chloroacetophenone phenylhydrazone; With trichlorophosphate;
N,N-dimethyl-formamide; at 60 - 70 ℃;
With trichlorophosphate; at 0 - 85 ℃; for 6h;
With trichlorophosphate; at 70 - 80 ℃;
With trichlorophosphate; at 50 - 60 ℃;
With trichlorophosphate; at 90 ℃; for 4h;
With trichlorophosphate; at 80 ℃; for 5h;
N,N-dimethyl-formamide; p-chloroacetophenone phenylhydrazone; With trichlorophosphate;
With sodium hydrogencarbonate; In water;
With trichlorophosphate; at 60 - 70 ℃; for 6h; Reflux;
With trichlorophosphate; In N,N-dimethyl-formamide; at 60 - 70 ℃; for 12h;
With trichlorophosphate; at 50 - 60 ℃; for 5h;
With potassium carbonate; trichlorophosphate; at 0 - 80 ℃; for 6h;
N,N-dimethyl-formamide; With trichlorophosphate; at 0 ℃; for 1.5h;
p-chloroacetophenone phenylhydrazone; at 0 - 20 ℃; for 6h; Reflux;
With trichlorophosphate; In ethanol; at 50 - 60 ℃; for 6h;
With trichlorophosphate; at 50 - 60 ℃; for 6h;
With trichlorophosphate; at 50 - 60 ℃;
With trichlorophosphate;
With trichlorophosphate; at 50 - 60 ℃;
N,N-dimethyl-formamide; With trichlorophosphate; at 0 - 5 ℃;
p-chloroacetophenone phenylhydrazone; at 70 - 80 ℃;
With trichlorophosphate; at 50 - 60 ℃;
With trichlorophosphate; at 0 - 80 ℃; for 6.5h;
With trichlorophosphate; at 50 - 60 ℃; for 5h;
With trichlorophosphate; In N,N-dimethyl-formamide;
With trichlorophosphate; at 50 - 60 ℃; for 5h;
With trichlorophosphate; at 50 - 60 ℃;
With trichlorophosphate; at 70 ℃; for 5h;
With trichlorophosphate; at 50 - 60 ℃; for 5h;
With trichlorophosphate; at 50 - 60 ℃; for 5h;
N,N-dimethyl-formamide; p-chloroacetophenone phenylhydrazone; With trichlorophosphate; at 80 ℃;
With water; sodium hydrogencarbonate;
With trichlorophosphate; at 80 - 85 ℃; for 5h;
With trichlorophosphate; at 0 - 90 ℃; for 1h;
With trichlorophosphate; at 70 - 75 ℃;
With trichlorophosphate; at 80 ℃;
N,N-dimethyl-formamide; p-chloroacetophenone phenylhydrazone; With trichlorophosphate; at 80 ℃;
With water; sodium hydrogencarbonate;
With trichlorophosphate; Heating;
With trichlorophosphate; at 10 - 90 ℃; for 8.5h;
With trichlorophosphate; at 70 - 80 ℃; for 1h;
N,N-dimethyl-formamide; With trichlorophosphate; at 0 ℃;
p-chloroacetophenone phenylhydrazone; at 85 ℃; for 6h;
N,N-dimethyl-formamide; p-chloroacetophenone phenylhydrazone; With trichlorophosphate; at 80 ℃;
With sodium hydrogencarbonate; In water;
With trichlorophosphate; at 90 ℃; for 2h;
N,N-dimethyl-formamide; p-chloroacetophenone phenylhydrazone; With trichlorophosphate; at 80 ℃;
With sodium hydrogencarbonate; In water;
With trichlorophosphate; Heating;
With trichlorophosphate; at 0 - 5 ℃;
With trichlorophosphate; at 0 - 20 ℃; for 12h;
With trichlorophosphate; at 0 - 70 ℃; for 6.5h;
N,N-dimethyl-formamide; p-chloroacetophenone phenylhydrazone; With trichlorophosphate; at 0 - 5 ℃; for 0.5h;
N,N-dimethyl-formamide; at 50 ℃;
With trichlorophosphate; at 0 - 65 ℃; for 5.5h;
With trichlorophosphate;
N,N-dimethyl-formamide; p-chloroacetophenone phenylhydrazone; With trichlorophosphate; at 0 - 70 ℃; for 3h;
With sodium hydrogencarbonate; In water;
With trichlorophosphate; at 90 ℃;
With trichlorophosphate; at 60 ℃; for 6h;
With trichlorophosphate; In N,N-dimethyl-formamide; at 50 - 60 ℃; for 5h;
With trichlorophosphate;
N,N-dimethyl-formamide; With trichlorophosphate;
p-chloroacetophenone phenylhydrazone; at 0 - 65 ℃; for 5.5h;
With trichlorophosphate; at 70 - 80 ℃;
With trichlorophosphate; for 5h; Reflux;
N,N-dimethyl-formamide; With trichlorophosphate; for 1h; Cooling with ice;
p-chloroacetophenone phenylhydrazone; at 20 ℃; for 0.5h;
at 80 ℃; for 4h;
N,N-dimethyl-formamide; p-chloroacetophenone phenylhydrazone; With trichlorophosphate; at 70 ℃; for 3h;
With water; sodium hydroxide;
With trichlorophosphate; at 50 - 60 ℃;
N,N-dimethyl-formamide; With trichlorophosphate; at -5 - 0 ℃; for 0.666667h;
p-chloroacetophenone phenylhydrazone; at -5 - 20 ℃; for 1.75h;
With trichlorophosphate; at 80 ℃; for 5h;
N,N-dimethyl-formamide; With trichlorophosphate; at 0 - 5 ℃;
p-chloroacetophenone phenylhydrazone; at 90 ℃; for 8h;
With trichlorophosphate; at 70 - 80 ℃;
With trichlorophosphate; at 60 ℃;
With trichlorophosphate; at 50 - 60 ℃;
With trichlorophosphate; at 50 - 60 ℃; for 6h;
With trichlorophosphate; at 0 - 60 ℃;
With trichlorophosphate;
5-amino-3-(4-chlorophenyl)-1-phenyl-1H-pyrazole-4-carbaldehyde
873913-39-4

5-amino-3-(4-chlorophenyl)-1-phenyl-1H-pyrazole-4-carbaldehyde

1-phenyl-3-(4-chlorophenyl)-4-pyrazolecarboxaldehyde
36663-00-0

1-phenyl-3-(4-chlorophenyl)-4-pyrazolecarboxaldehyde

Conditions
Conditions Yield
With hydrogenchloride; sodium nitrite; In methanol; water; for 3h; Cooling with ice; Inert atmosphere;
79%

2.What is the CAS number for 3,4,5-TRIHYDROXYBENZAMIDE ?

The CAS number of 3,4,5-TRIHYDROXYBENZAMIDE is 618-73-5.

More information of 3,4,5-TRIHYDROXYBENZAMIDE 618-73-5 are:

CAS?Number

618-73-5

Density

1.635 g/cm3

Melting Point

224-229 °C

Boiling Point

365 °C at 760 mmHg

Flash Point

174.6 °C

Vapor Pressure

7.68E-06mmHg at 25°C

Refractive Index

1.5500 (estimate)

HS CODE

2924299090

PSA

103.78000

LogP

0.60260

Pka

8.33±0.23(Predicted)

3.What are another words for 3,4,5-TRIHYDROXYBENZAMIDE ?

Synonyms?for?3,4,5-TRIHYDROXYBENZAMIDE 618-73-5:Gallamide(6CI,7CI,8CI);3,4,5-Trihydroxybenzamide;3,4,5-Trihydroxybenzoic acid amide;Gallic acid amide;NSC 1124;Gallamide;

4.What is the molecular formula of 3,4,5-TRIHYDROXYBENZAMIDE?

The chemical formula of ?3,4,5-TRIHYDROXYBENZAMIDE is?C7H7NO4 which containing 7 Carbon atoms,7 Hydrogen atoms,1 Nitrogen atoms and 4 Oxygen atoms,and the molecular weight of??3,4,5-TRIHYDROXYBENZAMIDE?is 169.137.

5.What is 3,4,5-TRIHYDROXYBENZAMIDE (618-73-5) used for?

3,4,5-TRIHYDROXYBENZAMIDE is a chemical compound characterized by a benzene ring with three hydroxyl groups and an amide functional group. It is known for its chelating properties, which make it a versatile agent in metal-ion complexation and a valuable building block in the synthesis of organic compounds. Its applications span across various fields, including pharmaceuticals, metal poisoning treatment, and as a potential antioxidant and anti-inflammatory agent in medicinal chemistry.

InChI:InChI=1/C7H7NO4/c8-7(12)3-1-4(9)6(11)5(10)2-3/h1-2,9-11H,(H2,8,12)

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6.Buy 3,4,5-TRIHYDROXYBENZAMIDE with the best price .

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