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N-Methylbenzamide

Product Name
N-Methylbenzamide
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
Formula Weight
135.16
MOL File
613-93-4.mol
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N-Methylbenzamide Property

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)
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Safety

Hazard Codes 
Xn
Risk Statements 
20/21/22-22
Safety Statements 
24/25
WGK Germany 
1
RTECS 
CV5570000
TSCA 
Yes
HS Code 
29242990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P405Store locked up.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
222798
Product name
N-Methylbenzamide
Purity
≥99%
Packaging
5g
Price
$68.1
Updated
2023/01/07
Sigma-Aldrich
Product number
222798
Product name
N-Methylbenzamide
Purity
≥99%
Packaging
10g
Price
$116
Updated
2023/01/07
Alfa Aesar
Product number
A18057
Product name
N-Methylbenzamide, 99%
Packaging
5g
Price
$57.65
Updated
2024/03/01
Alfa Aesar
Product number
A18057
Product name
N-Methylbenzamide, 99%
Packaging
25g
Price
$189.65
Updated
2024/03/01
Alfa Aesar
Product number
A18057
Product name
N-Methylbenzamide, 99%
Packaging
100g
Price
$745
Updated
2023/06/20
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N-Methylbenzamide Chemical Properties,Usage,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.

Synthesis Reference(s)

Synthetic Communications, 7, p. 549, 1977 DOI: 10.1080/00397917709409275
Tetrahedron Letters, 30, p. 451, 1989 DOI: 10.1016/S0040-4039(00)95225-0

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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N-Methylbenzamide Suppliers

Wako Pure Chemical Industries, Ltd.
Tel
--
Fax
--
Email
labchem-tec@wako-chem.co.jp
Country
Japan
ProdList
6819
Advantage
80
Kanto Chemical Co., Inc.
Tel
--
Fax
--
Email
reag-info@gms.kanto.co.jp
Country
Japan
ProdList
6756
Advantage
74
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View Lastest Price from N-Methylbenzamide manufacturers

Hebei Longbang Technology Co., Ltd
Product
N-Methylbenzamide 613-93-4
Price
US $6.00/kg
Min. Order
1kg
Purity
More than 99%
Supply Ability
2000KG/Month
Release date
2024-06-07
Hebei Yanxi Chemical Co., Ltd.
Product
N-METHYLBENZAMIDE 613-93-4
Price
US $10.00-8.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
2000kg
Release date
2024-03-21
Hebei Chuanghai Biotechnology Co,.LTD
Product
N-Methylbenzamide 613-93-4
Price
US $10.70/kg
Min. Order
10kg
Purity
99%
Supply Ability
10000kg
Release date
2024-08-20

613-93-4, N-MethylbenzamideRelated Search:


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