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Thermo Scientific Chemicals
Phenyl carbamate, 98+%
CAS: 622-46-8 | C7H7NO2 | 137.138 g/mol
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化學識別
CAS622-46-8
IUPAC Namephenyl carbamate
Molecular FormulaC7H7NO2
InChI KeyBSCCSDNZEIHXOK-UHFFFAOYSA-N
SMILESNC(=O)OC1=CC=CC=C1
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規格
規格表
規格表Appearance (Color)White
FormCrystals or powder or crystalline powder or fused solid
Assay (HPLC)≥98.0%
Identification (FTIR)Conforms
Phenyl 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.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Phenyl 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.
Solubility
Soluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from oxidizing agents. Stable under recommended storage conditions.
Phenyl 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.
Solubility
Soluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from oxidizing agents. Stable under recommended storage conditions.
RUO – Research Use Only
General References:
- ZH Fu.; Y Ono. Synthesis of methyl N-phenyl carbamate by methoxycarbonylation of aniline with dimethyl carbonate using Pb compounds as catalysts. Journal of molecular catalysis. 199491(3) , 399-405.
- RA Coss.; JD Pickett-Heaps. The effects of isopropyl N-phenyl carbamate on the green alga Oedogonium cardiacum I. Cell Division. The Journal of cell biology. 197463(1) , 84-98 .