Phenyl chloroformate
Phenyl chloroformate structure
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Common Name | Phenyl chloroformate | ||
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| CAS Number | 1885-14-9 | Molecular Weight | 156.566 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 186.5±9.0 °C at 760 mmHg | |
| Molecular Formula | C7H5ClO2 | Melting Point | -28 °C | |
| MSDS | Chinese USA | Flash Point | 79.0±12.1 °C | |
| Symbol |
GHS05, GHS06 |
Signal Word | Danger | |
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Kinetic study in water-ethylene glycol cationic, zwitterionic, nonionic, and anionic micellar solutions.
Langmuir 20(23) , 9945-52, (2004) The spontaneous hydrolysis of phenyl chloroformate was studied in water-ethylene glycol, EG, cationic, zwitterionic, nonionic, and anionic micellar solutions, the surfactants being tetradecyltrimethylammonium bromide, tetradecyl-N,N-dimethyl-3-ammonio-1-propa... |
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Preparation of 8,5'-O-cycloadenosine derivatives by reaction of 2',3'-O-isopropylideneadenosine with phenyl chloroformate or p-toluyl chloride.
Nucleic Acids Symp. Ser. (15) , 49-52, (1984) Reaction of 2',3'-O-isopropylideneadenosine with p-toluyl chloride in a mixture of methylene chloride and triethylamine afforded 2',3'-O-isopropylidene-N,N,5'-O-tri-p-toluyladenosine (8)(30%), 8,5'-O-cycloadenosine derivatives 9 (34%) and 10 (11%), and a cyan... |
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Ionizing power and nucleophilicity in water in oil AOT-based microemulsions.
Langmuir 21(17) , 7672-9, (2005) A study was carried out on the solvolysis of substituted phenyl chloroformates in AOT/isooctane/water microemulsions. (AOT is the sodium salt of bis(2-ethyhexyl)sulfosuccinate.) The results obtained have been interpreted by taking into account the distributio... |
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Development of quantitative assay for tissue levels of dolichyl phosphate.
Biochemistry 20(20) , 5831-6, (1981) A sensitive assay is described for quantitating dolichyl phosphate (Dol-P), the polyprenyl phospholipid which participates in N-linked glycosylation. The assay is based on a novel reaction of alkyl phosphates with phenyl chloroformate in which a monosubstitut... |
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Synthesis of L-2-oxothiazolidine-4-carboxylic acid.
Anal. Biochem. 138(2) , 449-50, (1984) An improved synthesis of L-2- oxothiazolidine -4-carboxylic acid is described. The new procedure, which leads to excellent yields of product, does not require the use of phosgene. The new method is thus less hazardous than the original one, and is readily ada... |
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Functional polymethacrylates as bacteriostatic polymers. Adelmann R, et al.
Eur. Polymer J. 45(11) , 3093-3107, (2009)
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Synthesis and ligand recognition of paracetamol selective polymers: semi-covalent versus non-covalent molecular imprinting. Rosengren-Holmberg JP, et al.
Org. Biomol. Chem. 7(15) , 3148-55, (2009)
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