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N-Methylbenzamide

N-Methylbenzamide Structure
CAS No.
613-93-4
Chemical Name:
N-Methylbenzamide
Synonyms
1MVR;N-Methylbenzenamide;Benzamide, N-methyl-;n-methyl-benzamid;N-METHYLBENZAMIDE;N-METHYLBENZAMIDE, 99+%;n-methylbenzenecarboxamide;N-MethylbenzaMide, 99+% 10GR;Benzamide, N-methyl- (6CI,7CI,8CI,9CI)
CBNumber:
CB0273752
Molecular Formula:
C8H9NO
Molecular Weight:
135.16
MOL File:
613-93-4.mol
MSDS File:
SDS
Modify Date:
2024/8/21 22:41:43

N-Methylbenzamide Properties

Melting point 76-78 °C (lit.)
Boiling point 167 °C/11 mmHg (lit.)
Density 1.1031 (rough estimate)
refractive index 1.5589 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility ethanol: soluble50mg/mL, clear, yellow-green
pka 15.00±0.46(Predicted)
form Solid
color White to off-white
Water Solubility Insoluble in water.
InChI InChI=1S/C8H9NO/c1-9-8(10)7-5-3-2-4-6-7/h2-6H,1H3,(H,9,10)
InChIKey NCCHARWOCKOHIH-UHFFFAOYSA-N
SMILES C(NC)(=O)C1=CC=CC=C1
CAS DataBase Reference 613-93-4(CAS DataBase Reference)
EPA Substance Registry System N-Methylbenzamide (613-93-4)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P305+P351+P338-P405-P501a
Hazard Codes  Xn
Risk Statements  20/21/22-22
Safety Statements  24/25
WGK Germany  1
RTECS  CV5570000
TSCA  Yes
HS Code  29242990
NFPA 704
0
1 0

N-Methylbenzamide price More Price(6)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 222798 N-Methylbenzamide ≥99% 613-93-4 5G ₹7112.03 2022-06-14 Buy
Sigma-Aldrich(India) 222798 N-Methylbenzamide ≥99% 613-93-4 5G ₹7112.03 2022-06-14 Buy
Sigma-Aldrich(India) 222798 N-Methylbenzamide ≥99% 613-93-4 10G ₹10803.35 2022-06-14 Buy
ALFA India ALF-A18057-22 N-Methylbenzamide, 99% 613-93-4 100g ₹61590 2022-05-26 Buy
ALFA India ALF-A18057-14 N-Methylbenzamide, 99% 613-93-4 25g ₹8479 2022-05-26 Buy
Product number Packaging Price Buy
222798 5G ₹7112.03 Buy
222798 5G ₹7112.03 Buy
222798 10G ₹10803.35 Buy
ALF-A18057-22 100g ₹61590 Buy
ALF-A18057-14 25g ₹8479 Buy

N-Methylbenzamide Chemical Properties,Uses,Production

Chemical Properties

N-methylbenzamide is an off-white crystalline solid.

Uses

N-Methylbenzamide is an important pesticide intermediate. It acts as a potent PDE10A (phosphodiesterase with a remarkable localization as the protein is abundant only in brain tissue) inhibitor.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

N-METHYLBENZAMIDE is an amide. Amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).

Fire Hazard

Flash point data concerning N-METHYLBENZAMIDE are not available, however, N-METHYLBENZAMIDE is probably combustible.

Synthesis

Add benzoic acid (977 mg, 8 mmol), dry DCM (20 mL) and catalytic amount of DMF in a 100 mL round-bottom flask. Cool the reaction mixture to 0°C and stir for 5 minutes. Add (COCl)2 (0.89 mL, 1.3 equiv.) dropwise to the reaction mixture and stir at room temperature for 4 hours. Concentrate the resulting mixture under reduced pressure to obtain acid chloride. Add catalytic amount of 4-dimethylaminopyridine, dry DCM (15 mL), MeNH2 (2 (M) in THF) (5.19 mL, 1.3 equiv.) and Et3N (1.56 mL, 1.4 equiv.) to the mixture in a 100 mL round-bottom flask. Cool the reaction mixture to 0°C. Add acid chloride (1.0 equiv.) dropwise at 0°C. Stir the reaction mixture at room temperature for 12 hours. Add water (40 mL) and seperate the organic layer. Extract the aqueous layer with DCM (3 x 30 mL). Wash the combined organic layer with saturated aqueous NaHCO3 (30 mL) solution followed by water (30 mL). Dry the organic layer over Na2SO4 and concentrated under reduced pressure. Purify the crude mass by silica gel column chromatography (20% ethyl acetate in hexane as eluent) to obtain N-methylbenzamide. DOI: 10.1002/anie.202203539

N-Methylbenzamide Preparation Products And Raw materials

Raw materials

Preparation Products

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