68835-89-2

Usage

Uses

Used in Pharmaceutical Industry:
DI-TERT-AMYL DICARBONATE is used as a protecting group for amines in organic synthesis for the reason that it facilitates the synthesis of complex organic compounds by temporarily masking the amine functional groups in drug molecules.
Used in Carbon Capture Technologies Research:
DI-TERT-AMYL DICARBONATE is used as a subject of study for its potential application in carbon capture technologies, with the aim of exploring its effectiveness in capturing and storing carbon dioxide to mitigate climate change.

InChI:InChI=1/C12H22O5/c1-7-11(3,4)16-9(13)15-10(14)17-12(5,6)8-2/h7-8H2,1-6H3

Upstream product

• 124-38-9 carbon dioxide 

Downstream Products

• 114779-81-6 N-Amoc-DL-α-methyl tryptophan 
• 82882-70-0 N^α-tert-amyloxycarbonyl-N^im-tritylhistidine 
• 1053629-62-1 C₄₈H₆₁Cl₆NO₁₈ 
• 1206968-10-6 1,1-Dimethylpropyl 4-[2-(4-methanesulfonylphenoxymethyl)-pyridin-5-yl]piperidine-1-carboxylate 
• 114779-60-1 N-Amoc-DL-α-methyl tryptophanyl-L-phenylalaninepiperidineamide 
• 114779-52-1 N-Amoc-DL-α-methyl tryptophanyl-2-(3,4-dichlorophenyl)ethylamide 
• 114779-39-4 N-Amoc-DL-α-methyl tryptophanyl-L-(1-hydroxymethyl-2-phenyl)ethylamide 
• 114779-50-9 N-Amoc-DL-α-methyl tryptophanyl-2-(4-methoxyphenyl)ethylamide 
• 114779-51-0 N-Amoc-DL-α-methyl tryptophanyl-2-(4-chlorophenyl)ethylamide 
• 129397-53-1 N-Amoc-DL-α-methyl tryptophanyl-2-(4-methylphenyl)ethylamide 
• 129397-52-0 1,1-dimethylpropyl (+/-)-<1-(1H-indol-3-ylmethyl)-1-methyl-2-oxo-2-<(phenylethyl)amino>ethyl>carbamate 

Relevant academic research and scientific papers

Pyrocarbonic acid diesters and the preparation and use thereof

The invention relates to the preparation of pyrocarbonic acid diesters by an improved process and to the novel pyrocarbonic acid diesters prepared according to said process as well as to the use thereof.The core of the invention is a process for the preparation of a pyrocarbonic acid diester of formula (I) wherein R1 and R1′ are each independently of the other branched or straight-chain C1-C24alkyl, C3-C24alkenyl, C3-C24alkynyl, C4-C12cycloalkyl, C4-C12cycloalkenyl or C7-C24aralkyl, each of which is unsubstituted or substituted by one or more than one substituent which is inert under the reaction conditions,by reacting at least one ester carbonate of formula (II) ?with 40-50 mol % of a sulfochloride of formula (IV) ?in the presence of 0.8-5 mol % of a catalyst of formula (V) and with minor amounts of a heterocyclic aromatic amine in a nonpolar inert solvent,in which process the amount of heterocyclic aromatic amine is 1-3 mol % and the reaction is carried out in the temperature range from ?10° C. to ±25° C., all molar amounts being based on 100 mol % of ester carbonate of formula (II).