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328766

N-Methyl-N-phenylcarbamoyl chloride

98%

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About This Item

Linear Formula:
C6H5N(CH3)COCl
CAS Number:
4285-42-1
Molecular Weight:
169.61
NACRES:
NA.22
PubChem Substance ID:
24859745
UNSPSC Code:
12352100
EC Number:
224-288-4
MDL number:
MFCD00000634
Assay:
98%

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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

100

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N-Methyl-N-phenylcarbamoyl chloride 98%

Sigma-Aldrich

328766

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4-Morpholinecarbonyl chloride 98%

Sigma-Aldrich

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4-Morpholinecarbonyl chloride

3,5-Dimethoxybenzoyl chloride 97%

Sigma-Aldrich

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3,5-Dimethoxybenzoyl chloride

4-Chloropyridine N-oxide 98%

Sigma-Aldrich

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4-Chloropyridine N-oxide

assay

98%

assay

98%

assay

97%

assay

98%

Quality Level

100

Quality Level

200

Quality Level

100

Quality Level

100

bp

280 °C (lit.)

bp

137-138 °C/33 mmHg (lit.)

bp

157-158 °C/16 mmHg (lit.)

bp

-

mp

87-90 °C (lit.)

mp

-

mp

43-46 °C (lit.)

mp

160 °C (dec.) (lit.)

storage temp.

2-8°C

storage temp.

-

storage temp.

-

storage temp.

2-8°C

functional group

amine

functional group

chloro, ether

functional group

acyl chloride

functional group

chloro

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.[1] Iridium-catalyzed annulation of N-methyl-N-phenylcarbamoyl chloride with internal alkyne was reported.[2]

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

hcodes

H314,H335

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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Certificates of Analysis (COA)

Lot/Batch Number
MKCS0072
MKCS7279
MKCK3595
MKCK0458
MKCC0036

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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)
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

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