carbaniloyl chloride, n-methyl-

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Names

[ Name ]:
carbaniloyl chloride, n-methyl-

[Synonym ]:
N-methyl-N-phenylcarbamyl chloride
Carbamic chloride, methyl(phenyl)-
N-phenyl-N-methylcarbamoyl chloride
MFCD00000634
N-METHYL-N-PHENYLCARBAMOYLCHLORIDE
Carbamoyl chloride,methylphenyl
Carbaniloyl chloride,N-methyl
EINECS 224-288-4
Carbamoyl chloride, methylphenyl-
Methyl(phenyl)carbamic chloride
N-methyl-N-phenyl-carbamic acid chloride
Carbamic chloride, methylphenyl-
carbaniloyl chloride, n-methyl-
1-phenylcyclopropanecarbonyl chloride
N-phenyl-N-methylcarbamyl chloride
Carbamic chloride,methylphenyl
Methylphenylcarbamoyl chloride

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
280.0±9.0 °C at 760 mmHg

[ Melting Point ]:
87-90ºC(lit.)

[ Molecular Formula ]:
C₈H₈ClNO

[ Molecular Weight ]:
169.608

[ Flash Point ]:
123.1±18.7 °C

[ Exact Mass ]:
169.029449

[ PSA ]:
20.31000

[ LogP ]:
1.99

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.583

[ Storage condition ]:
2-8°C

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS05, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314-H335

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges

[ Hazard Codes ]:
C: Corrosive;

[ Risk Phrases ]:
34-36/37

[ Safety Phrases ]:
26-27-28-36/37/39-45

[ RIDADR ]:
UN 3261 8/PG 2

[ WGK Germany ]:
3

[ HS Code ]:
2903999090

Synthetic Route

Click to get detail synthetic route

Customs

[ HS Code ]: 2903999090

[ Summary ]:
2903999090 halogenated derivatives of aromatic hydrocarbons VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

Iridium-catalyzed annulation of N-arylcarbamoyl chlorides with internal alkynes.

J. Am. Chem. Soc. 132(28) , 9602-3, (2010)

An iridium complex successfully catalyzed the annulation of various N-arylcarbamoyl chlorides with internal alkynes to afford 2-quinolones in good to excellent yields. The present reaction is widely a...

Solvolyses of N-Methyl-N-phenylcarbamoyl Chlorides with Electron Acceptor Substituents in Aqueous Binary Mixtures. Koo IS, et al

Bull. Korean Chem. Soc. 22(8) , 842-46, (2001)

Cyclopropaneethanimidoyl chloride, N-methyl-alpha-oxo- (9CI)
N-methyltrifluoroacetimidoyl chloride
N-methylacetamidinium chloride
N-phenacylcarbamoyl chloride
ISOBUTYL(METHYL)SULFAMOYL CHLORIDE
methyl-trioctyl-azanium chloride
2-(Difluoromethoxy)-5-(difluoromethyl)benzo[d]oxazole
2-(Difluoromethyl)-3-fluoro-4-hydroxypyridine-6-carboxamide
5-(2-Bromoethoxy)-2-methylquinazoline
5-((3,5-Dichloropyridin-4-yl)thio)-N-(4-methylbenzyl)-4-nitrothiazole-2-carboxamide
5-((3,5-Dichloropyridin-4-yl)thio)-N-(3-fluorobenzyl)-4-nitrothiazole-2-carboxamide
N-Benzyl-1-(5-((3,5-dichloropyridin-4-yl)thio)-4-nitrothiazol-2-yl)ethanamine
2-(Difluoromethyl)naphthalene-6-acetic acid
1-(5-((3,4-Dimethoxyphenyl)thio)-4-nitrothiazol-2-yl)ethanone
1-(5-((2,6-Dichlorophenyl)thio)-4-nitrothiazol-2-yl)ethanone
N-Benzyl-5-((3,5-dichloropyridin-4-yl)thio)-4-nitrothiazole-2-carboxamide

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