328766
N-Methyl-N-phenylcarbamoyl chloride
98%
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About This Item
Linear Formula:
C6H5N(CH3)COCl
CAS Number:
Molecular Weight:
169.61
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
224-288-4
MDL number:
Assay:
98%
Product Name
N-Methyl-N-phenylcarbamoyl chloride, 98%
InChI key
CPGWSLFYXMRNDV-UHFFFAOYSA-N
InChI
1S/C8H8ClNO/c1-10(8(9)11)7-5-3-2-4-6-7/h2-6H,1H3
SMILES string
CN(C(Cl)=O)c1ccccc1
assay
98%
bp
280 °C (lit.)
mp
87-90 °C (lit.)
functional group
amine
chloro
storage temp.
2-8°C
Quality Level
Related Categories
General description
Solvolyses of N-methyl-N-phenylcarbamoyl chlorides in aqueous binary mixtures of acetone, ethanol, methanol and in water, D2O and 50% D2O-CH3OD were investigated. Iridium-catalyzed annulation of N-methyl-N-phenylcarbamoyl chloride with internal alkyne was reported.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Tomohiro Iwai et al.
Journal of the American Chemical Society, 132(28), 9602-9603 (2010-06-30)
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 applicable to substrates with various functionalities. An amide-iridacycle complex was isolated, and it
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), 842-846 (2001)
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