T-butyl Carbonate
14418 Adapted Stein Brown method Melting Pt deg C. Carbonic acid tert-butyl ester.
Allyl Tert Butyl Carbonate C8h14o3 Pubchem
Carbonic Acid tert-Butyl Phenyl Ester.
T-butyl carbonate. Dicarbonate de bis 2-méthyl-2-propanyl e French ACDIUPAC Name di-t-Butyl dicarbon ate. The BOC group can be added to the amine under aqueous conditions using di-tert-butyl dicarbonate in the presence of a base such as sodium carbonate. Carbonic acidtert-butyl esterphenyl ester.
Structure properties spectra suppliers and links for. Find t-butyl carbonate and related products for scientific research at MilliporeSigma. The unsymmetrical dialkyl carbonate may be methyl t-butyl carbonate ethyl t-butyl carbonate methyl t-amyl carbonate or ethyl t-amyl carbonate.
525 Mean VP of Antoine. Tert -Butyl alcohol is a colorless solid which melts near room temperature and has a camphor -like odor. The mixture is stirred for 15 minutes.
Di- tert -butyl pyrocarbonate Boc anhydride Di-tert-butyl dicarbonate. T-butyl phenyl carbonate tert-butylphenylcarbonate 2-methyl-2-propanyl phenyl carbonate carbonic acid 11-dimethylethyl phenyl ester pubchem13300 acmc-209nuo phenyl t-butyl carbonate uxwvqhxkkogtsy-uhfffaoysa tert-butyl phenyl carbonate carbonic acid tert-butylphenyl ester. Boiling Pt deg C.
Log Octanol-Water Partition Coef SRC. Pyrocarbonic acid di-tert-butyl ester. Carbonic acid 11-dimethylethoxycarbonyl 11-dimethylethyl ester ACDIndex Name di tert-butyl carbonate.
It is miscible with water ethanol and diethyl ether. Tert-Butyl phenyl carbonate was used in determination of octanol-water partition coefficients by microemulsion electrokinetic chromatographyIt was also used in the synthesis of 2-nitroindoles. 5 ml of 2-methyl-2-propanol t-butyl alcohol is put in an Erlenmeyer flask the flask is put over a stir motor with stir bar and commence stirring.
-8845 Mean or Weighted MP VPmm Hg25 deg C. Butyl chloride washed with aqueous sodium hydrogen carbonate. Chemsrc provides tert-Butyl phenyl carbonateCAS6627-89-0 MSDS density melting point boiling point structure formula molecular weight.
Di-tert-butyl dicarbonate can be analyzed by this reverse phase RP HPLC method with simple conditions. Protection of the amine can also be accomplished in acetonitrile solution using 4. For Mass-Spec MS compatible applications the phosphoric acid needs to be replaced with formic acid.
The mobile phase contains an acetonitrile MeCN water and phosphoric acid. Log Kow KOWWIN v167 estimate 160 Boiling Pt Melting Pt Vapor Pressure Estimations MPBPWIN v142. Tert-Butyl alcohol is the simplest tertiary alcohol with a formula of CH 3 3 COH sometimes represented as t -BuOH.
OO-t-Butyl O-2-ethylhexyl monoperoxy carbonate. Dicarbonic acid bis11-dimethylethyl ester. LuperoxR TBEC tert-Butylperoxy 2-ethylhexyl carbonate 95.
Why was the tert-butyl chloride washed with aqueous sodium hydrogen carbonate. Tert-Butyl methyl carbonate C6H12O3 CID 545995 - structure chemical names physical and chemical properties classification patents literature biological. Unsymmetrical dialkyl carbonates are blended with hydrocarbon liquid fuels such as gasoline to provide fuel compositions having improved octane number and anti-knock characteristics.
Molbase found 10 di-tert-butyl carbonate product information for you including di-tert-butyl carbonate formula di-tert-butyl carbonate CAS number di-tert-butyl carbonate supplier information. TButyl 2Pyridon1yl Carbonate and Benzyl 2Pyridon1yl Carbonate. Tert-Butylperoxy 2-ethylhexyl carbonate CAS 34443-12-4 plays a role as initiator for the solution copolymerization of acrylates and methcrylates in the temperature range of 100-170.
13mL of concentrated HCl is added into the flask. It was used as reagent for mono-Boc protection of αω-diamines. Slightly soluble in water.
Predicted data is generated using the US Environmental Protection Agencys EPISuite. Tert-Butyl phenyl carbonate 98. What is the mechanism of the reaction between tert-butyl alcohol and HCl.
New Amino Protective Reagents for tButoxycarbonylation and Benzyloxycarbonylation of Amines and Amino Acids. A strong acid probably HCl was used in the synthesis of the t-butyl chloride. It is one of the four isomers of butanol.
Tert-Butylperoxy 2-ethylhexyl carbonate CAS 34443-12-4 can also be applied as an initiator for the bulk and suspension copolymerization of acrylates and methcrylates. NaHCO3 neutralizes the excess HCl. The tert-butyloxycarbonyl protecting group or tert-butoxycarbonyl protecting group BOC group is a protecting group used in organic synthesis.
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