N-Methyl-N-phenylcarbamic chloride
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N-Methyl-N-phenylcarbamic chloride
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CAS No:
4285-42-1
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Formula:
C8H8ClNO
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Chemical Name:
N-Methyl-N-phenylcarbamic chloride
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Synonyms:
Carbamic chloride,N-methyl-N-phenyl-;Carbaniloyl chloride,N-methyl-;Carbamic chloride,methylphenyl-;N-Methyl-N-phenylcarbamic chloride;Methylphenylcarbamoyl chloride;N-Methyl-N-phenylcarbamoyl chloride;N-Methyl-N-phenylcarbamic acid chloride;NSC 165671;(Methyl)phenylcarbamic chloride;1301139-25-2
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CAS No:
N-Methyl-N-phenylcarbamic chloride Basic Attributes
169.61
169.61
224-288-4
165671
DTXSID7063396
29242998
Safety Information
UN 3261 8/PG 2
3
34-36/37
26-27-28-36/37/39-45
C
P261-P280-P305 + P351 + P338-P310
H314-H335
|Danger|H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]|P260, P261, P264, P271, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 39 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
N-Methyl-N-phenylcarbamic chloride Use and Manufacturing
Derived from the reaction of N-methylaniline and phosgene. First, phosgene was introduced into ethyl acetate until saturated, and then the N-methylaniline-ethyl acetate solution was slowly added while continuing to introduce phosgene. After the reaction was completed, the ethyl acetate was distilled off, and the obtained crude product was recrystallized from ethanol. The yield is about 80%.
Used in organic synthesis.
Carbamic chloride, N-methyl-N-phenyl-: INACTIVE
Computed Properties
Molecular Weight:169.61
XLogP3:2.2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:169.0294416
Monoisotopic Mass:169.0294416
Topological Polar Surface Area:20.3
Heavy Atom Count:11
Complexity:143
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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N-Methyl-N-phenylcarbamic chloride
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