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4-METHYL-3-NITROBENZAMIDE
- Name 4-METHYL-3-NITROBENZAMIDE
- CAS 19013-11-7
- Purity 99%
Product Details
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1.What is the 4-METHYL-3-NITROBENZAMIDE ?
Used in Organic Synthesis:
4-METHYL-3-NITROBENZAMIDE is used as a building block for the synthesis of other chemical compounds, playing a crucial role in the development of new organic molecules.
Used in Pharmaceutical Industry:
4-METHYL-3-NITROBENZAMIDE is used as a precursor in the synthesis of pharmaceutical compounds, contributing to the discovery and development of new drugs.
Used in Agrochemical Industry:
4-METHYL-3-NITROBENZAMIDE is used as a starting material for the production of agrochemicals, such as pesticides and herbicides, to improve crop protection and yield.
Used in Materials Science:
4-METHYL-3-NITROBENZAMIDE is used as a component in the development of new materials with specific properties, such as polymers, coatings, and adhesives.
Used as a Reagent in Chemical Reactions:
4-METHYL-3-NITROBENZAMIDE is used as a reagent to facilitate various chemical reactions, enabling the synthesis of target compounds and improving reaction efficiency.
Used as a Precursor for Synthesis of Organic Compounds:
4-METHYL-3-NITROBENZAMIDE is used as a precursor in the synthesis of a wide range of organic compounds, including intermediates and final products in various chemical processes.
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96-98-0
4-methyl-3-nitrobenzoic acid
-
-
19013-11-7
4-methyl-3-nitrobenzamide
| Conditions | Yield |
|---|---|
|
With
phosphorus pentachloride;
Behandlung des erhaltenen Chlorids mit konz. Ammoniak;
|
|
|
4-methyl-3-nitrobenzoic acid;
With
N,N-dimethyl-formamide; 1,1'-carbonyldiimidazole;
In
tetrahydrofuran;
for 0.75h;
With
ammonia;
In
tetrahydrofuran; water;
at 20 ℃;
for 24h;
|
|
|
4-methyl-3-nitrobenzoic acid;
With
1,1'-carbonyldiimidazole;
In
tetrahydrofuran; N,N-dimethyl-formamide;
for 0.75h;
With
ammonia;
In
tetrahydrofuran; water; N,N-dimethyl-formamide;
at 20 ℃;
for 24h;
|
-
-
41252-97-5
4-iodo-2-nitrotoluene
-
-
potassium ferrocyanide
-
-
19013-11-7
4-methyl-3-nitrobenzamide
| Conditions | Yield |
|---|---|
|
With
water; potassium carbonate;
In
dimethyl sulfoxide;
at 110 ℃;
for 12h;
|
80%
|
2.What is the CAS number for 4-METHYL-3-NITROBENZAMIDE ?
The CAS number of 4-METHYL-3-NITROBENZAMIDE is 19013-11-7.
More information of 4-METHYL-3-NITROBENZAMIDE 19013-11-7 are:
|
CAS?Number |
19013-11-7 |
|
Density |
1.322 g/cm3 |
|
Melting Point |
164-165°C |
|
Boiling Point |
291.7 °C at 760 mmHg |
|
Flash Point |
130.2 °C |
|
Vapor Pressure |
0.00192mmHg at 25°C |
|
Refractive Index |
1.599 |
|
HS CODE |
2924299090 |
|
PSA |
88.91000 |
|
LogP |
2.22560 |
3.What are another words for 4-METHYL-3-NITROBENZAMIDE ?
Synonyms?for?4-METHYL-3-NITROBENZAMIDE 19013-11-7:p-Toluamide,3-nitro- (8CI);4-Methyl-3-nitrobenzamide;
4.What is the molecular formula of 4-METHYL-3-NITROBENZAMIDE?
The chemical formula of ?4-METHYL-3-NITROBENZAMIDE is?C8H8N2O3 which containing 8 Carbon atoms,8 Hydrogen atoms,2 Nitrogen atoms and 3 Oxygen atoms,and the molecular weight of??4-METHYL-3-NITROBENZAMIDE?is 180.163.
5.What is 4-METHYL-3-NITROBENZAMIDE (19013-11-7) used for?
4-METHYL-3-NITROBENZAMIDE, a chemical compound with the molecular formula C8H8N2O3, is a derivative of benzamide featuring a methyl group and a nitro group attached to the benzene ring. It is widely utilized in organic synthesis and research as a building block for creating other chemical compounds, with potential applications in pharmaceuticals, agrochemicals, and materials science. Additionally, it serves as a reagent in chemical reactions and a precursor for the synthesis of various organic compounds. Due to its moderate toxicity, it should be handled with caution in laboratory settings.
InChI:InChI=1/C8H8N2O3/c1-5-2-3-6(8(9)11)4-7(5)10(12)13/h2-4H,1H3,(H2,9,11)
Relevant articles related to 4-METHYL-3-NITROBENZAMIDE:
|
Article |
Source |
|
1-(PIPERIDIN-4-YL)-1H-INDOLE DERIVATIVE |
- Page/Page column 32, (2010/11/28) |
|
Labelled compounds of interest as antitumour agents - VI. Isotopically efficient syntheses of [15N]-nitrothiophenecarboxamides |
Shinkwin, Anne E.,Threadgill, Michael D. , p. 1015 - 1020 (2007/10/03) |
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