CAS 1885-14-9
:Chloroformiate de phényle
- Chlorameisensaeure-Phenylester
- Chlorocarbonic acid phenyl ester
- Chloroformate, Phenyl
- Chloroformiate de phenyle
- Chloroformic acid phenyl ester
- Cloroformiato De Fenilo
- Formic acid, chloro-, phenyl ester
- Nsc 210946
- Phenyl Chloroformate
- Phenyl carbonochloridate
- Phenyl chlorocarbonate
- Phenylchlorformiat
- Phenylchloroformic acid
- Phenyloxycarbonyl chloride
- Voir plus de synonymes
Phenyl Chloroformate
CAS :Formule :C7H5ClO2Degré de pureté :>98.0%(GC)(T)Couleur et forme :Colorless to Light yellow clear liquidMasse moléculaire :156.57Phenyl chloroformate, 99%
CAS :Phenyl chloroformate is used in the synthesis of poly(2-(phenoxycarbonyloxy)ethyl methacrylate) and phenyl-(4-vinylphenyl) carbonate. It acts as a precursor of phenyl mixed anhydrides which are used in peptide coupling reactions. It serves as a dehydrating reagent for the conversion of primary amide
Formule :C7H5ClO2Degré de pureté :99%Couleur et forme :Clear colorless, LiquidMasse moléculaire :156.57Phenyl Chloroformate
CAS :Produit contrôléApplications Phenyl chloroformate is a corrosive liquid that is used to synthesize Urazole, a five membered heterocyclic compound that reacts with aldoses to form α and β pyranosides and furanosides. Phenyl chloroformate is also used as a reagent to prepare Sorafenib (S676850), a multikinase inhibitor that targets the tumour and tumour vasculature in patients with melanoma.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Boettecher, B. & Meister, A.: Anal. Biochem., 138, 449 (1984); Chai, W., et al.: Tetrahedron Lett., 53, 3514 (20112); Eisen, T., et al.: Brit. J. Cancer, 95, 581 (2006); Kolb, V., et al.: J. Mol. Evol., 38, 549 (1994); Llovet, J., et al.: Engl. J. Med., 359, 378 (2008)Formule :C7H5ClO2Couleur et forme :NeatMasse moléculaire :156.57Phenyl chloroformate
CAS :Phenyl chloroformate is a phenyl compound that is used as a reagent for cationic polymerization. This chemical reacts with amines to form an N-substituted amide in the presence of hydrogen chloride. The mechanism of this reaction is based on nucleophilic substitutions by the hydroxyl group of the phenyl group. Phenyl chloroformate has been used in the synthesis of fatty acids, which are important components of metabolic disorders such as diabetes mellitus type 2.Formule :C7H5ClO2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :156.57 g/mol





