Phenyl carbamate

Phenyl carbamate Basic information
Product Name:Phenyl carbamate
Synonyms:PHENYL CARBAMATE;o-Phenyl carbamate;Phenyl carbamate,97%;Phenylcarbamate,98+%;CARBAMICACID,PHENYLESTER;Phenyl carbaMate 97%;Phenyl carbamate ISO 9001:2015 REACH
CAS:622-46-8
MF:C7H7NO2
MW:137.14
EINECS:210-737-1
Product Categories:Nitrogen Compounds;Organic Building Blocks;Protected Amines
Mol File:622-46-8.mol
Phenyl carbamate Structure
Phenyl carbamate Chemical Properties
Melting point 149-152 °C(lit.)
Boiling point 251.96°C (rough estimate)
density 1.2528 (rough estimate)
refractive index 1.5030 (estimate)
storage temp. Sealed in dry,Room Temperature
pka12.33±0.50(Predicted)
Water Solubility Soluble in water.
BRN 2042627
CAS DataBase Reference622-46-8(CAS DataBase Reference)
Safety Information
Safety Statements 24/25
WGK Germany 3
HS Code 29242998
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
Phenyl carbamate Usage And Synthesis
Chemical Propertieswhite to very slightly pink crystalline flakes
UsesPhenyl carbamate is used as various phenyl carbamate esters derived from amino acids, a dipeptide and amino acid esters and amides were prepared and assessed as potential prodrugs with the aim of protecting phenolic drugs against first-pass metabolism following per oral administration.
A tin-catalyzed transcarbamoylation
A tin-catalyzed transcarbamoylation of primary and secondary alcohols with phenyl carbamate proceeds smoothly in toluene at 90℃ to generate the corresponding carbamates in good yields. This mild method exhibits a broad functional-group tolerance.
Y. Ichikawa, Y. Morishita, S. Kusaba, N. Sakiyama, Y. Matsuda, K. Nakano, H. Kotsuki, Synlett, 2010, 1815-1818.
http://dx.doi.org/10.1055/s-0030-1258102
UsesPhenyl Carbamate is a robust, inert to Pd-catalysis reagent which are useful for arene functionalization/site-selective cross-coupling reactions.
DefinitionChEBI: Phenyl carbamate is an aromatic ether.
DIPHENYL AZO DICARBOXYLATE 1-NAPHTHYL N-PROPYLCARBAMATE 4-[(1,3,5-TRIMETHYL-1H-PYRAZOL-4-YL)METHYL]PHENYL N-[4-(TRIFLUOROMETHOXY)PHENYL]CARBAMATE 2-[[5-CHLORO-1-(4-METHOXYPHENYL)-6-OXO-1,6-DIHYDRO-4-PYRIDAZINYL](METHYL)AMINO]ETHYL N-[3-(TRIFLUOROMETHYL)PHENYL]CARBAMATE 4-(acetylamino)phenyl methyl(phenyl)carbamate 3-NITRO-4-PHENOXYBENZYL N-[3-(TRIFLUOROMETHYL)PHENYL]CARBAMATE PHENYL ISOCYANATOFORMATE 2-CHLOROPHENYL PHENYL URETHANE PHENYL N-(4-CHLOROPHENYL)CARBAMATE BDMC phenyl piperidine-1-carboxylate phenyl N-(4-bromophenyl)carbamate TERT-BUTYL [4-(CHLOROSULFONYL)PHENYL]CARBAMATE [2-(PHENYLSULFANYL)-3-PYRIDINYL]METHYL N-[3-(TRIFLUOROMETHYL)PHENYL]CARBAMATE 3-(Boc-amino)phenylboronic acid pinacol ester, tert-Butyl-N-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamate PHENYL 3-NITROPHENYLCARBAMATE Phenyl carbamate N,N-DIMETHYL-2,4,5-TRICHLOROPHENYL CARBAMATE

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