Compounds > bis(tert-butoxycarbonyl)oxide
Page last updated: 2024-12-07

bis(tert-butoxycarbonyl)oxide

Description

bis(tert-butoxycarbonyl)oxide: reagent fortert-butylcarbonylating amino acids [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID90495
CHEBI ID48500
SCHEMBL ID5452
MeSH IDM0089565

Synonyms (200)

Synonym
carbonic acid tert-butoxycarbonyl tert-butyl ester
di(tert-butyl) carbonate
pyrocarbonic acid di-tert-butyl ester
di-tert-butyldicarbonate
bis(tert-butoxycarbonyl)oxide
dicarbonic acid, bis(1,1-dimethylethyl) ester
einecs 246-240-1
di-tert-butyl dicarbonate
tert-butoxycarbonyl anhydride
ccris 2598
boc-anhydride
CHEBI:48500
24424-99-5
boc2o
di-tert-butyl dicarbonate, reagentplus(r), 99%
di-tert-butyl dicarbonate, reagentplus(r), >=99%
D3880
di-tert-butyl pyrocarbonate
D3879
D3878
di-t-butyl pyrocarbonate
di-t-butyl dicarbonate
D1547
diboc
boc anhydride
tert-butyl (2-methylpropan-2-yl)oxycarbonyl carbonate
AKOS000121490
di-tert-butyl dicarbonate 2.0m in ethyl acetate
di-tert-butyl dicarbonate 1.0m in thf
di-tert-butyl dicarbonate 2.0m in thf
di-tert-butyl dicarbonate 2.0m in dichloromethane
z10q236c3g ,
ec 246-240-1
dicarbonic acid, 1,3-bis(1,1-dimethylethyl) ester
unii-z10q236c3g
di-tert-butyl pyrocarbonate; dicarbonic acid bis(1,1-dimethylethyl)ester; pyrocarbonic acid di-tert-butyl ester
BP-20551
FT-0625356
AM20090273
tert-butyl (tert-butoxycarbonyloxy)formate
di-tert-butyl dicarbonate [mi]
dicarbonic acid c,c'-bis(1,1-dimethylethyl) ester
di-tert-butyl oxydiformate
SCHEMBL5452
tert-butoxycarbonyl tert-butyl carbonate
di-tert-butyidicarbonate
di(1,1-dimethylethyl)dicarbonate
bis(1,1-dimethylethyl) dicarbonoate
di-tert-butyldicarbonat
di (tert-butyl)dicarbonate
t-boc2o
di-tert. butyl pyrocarbonate
di(tert-butyl)pyrocarbonate
di-tertbutylpyrocarbonate
ditertiary-butyldicarbonate
ditert butyldicarbonate
di-tert-butly-dicarbonate
di-tert-buyldicarbonate
di-tertiarybutyl dicarbonate
ditertiary butyl dicarbonate
di-tert-butlydicarbonate
di-tert. butyl-dicarbonate
di-tertiarybutyldicarbonate
di-tertiary-butyldicarbonate
di-tert.-butylpyrocarbonate
di-tert.-butyldicarbonate
di(tert-butyl) dicarbonate
di tert.-butyldicarbonate
di-tert-butyl di carbonate
di tert butyl dicarbonate
bis(tert-butyl)dicarbonate
di-tert-butyl-pyrocarbonate
bis(t-butoxycarbonyl) oxide
di-(t-butyl)dicarbonate
pyrocarbonic acid di-tert.butyl ester
bis(t-butyl)pyrocarbonate
bis(tert-butyl) dicarbonate
di-tert-butyl dicarbonat
di-ter-butyl dicarbonate
di-terbutyl dicarbonate
di(t-butyl)dicarbonate
ditertiary butyldicarbonate
ditert-butyl-dicarbonate
diterbutyldicarbonate
tert-butyl(tert-butoxycarbonyloxy)formate
di-tert -butyldicarbonate
pyrocarbonic acid-di-tert-butyl ester
bis (1,1-dimethylethyl) dicarbonate
ditert-butyldicarbonate
di-tertiary-butyl dicarbonate
di t-butyl dicarbonate
(tboc)2o
tboc2o
ditertiarybutyl dicarbonate
di-t -butyldicarbonate
di-tert.-butyldicarbonat
bis(1,1-dimethylethyl)dicarbonoate
di-tert.butylpyrocarbonate
(2-methylpropan-2-yl)oxycarbonyl tert-butyl carbonate
di-(tert-butyl) dicarbonate
di-tert.butyldicarbonate
ditert butyl dicarbonate
dicarbonic acid di(t-butyl) ester
di-tertiary butyl-dicarbonate
bis(1,1-dimethylethyl) dicarbonate
di-tert butyl dicarbonate
di tert-butyldicarbonate
di-tert.butyl pyrocarbonate
di-t-butyldicarbonate
di-tert.-butyl-dicarbonate
di-tert.butyl-dicarbonat
ditertbutyldicarbonate
di-tertbutyl dicarbonate
di-tert-butylpyrocarbonate
di-tert.butyl-dicarbonate
di-tert-butydicarbonate
diterbutyl-dicarbonate
di-tertbutyl-pyrocarbonate
di-t-butyl-dicarbonate
di-(tert-butyl)dicarbonate
di-tert.butyl dicarbonate
ditert-butyl dicarbonate
di-t butyl dicarbonate
di(tert-butyl)dicarbonate
di tert butyldicarbonate
o(boc)2
di-tertbutyl-dicarbonate
(tbuo2c)2o
tert-butoxycarboxylic acid anhydride
ditertbutyl dicarbonate
diterbutyl dicarbonate
ditert.butyl dicarbonate
di-t-butylpyrocarbonate
bis(1,1-dimethylethyl)dicarbonate
di-tert.-butyl dicarbonate
di tertiary butyl dicarbonate
tert-butyl [(tert-butyl)oxycarbonyloxy]formate
di-tert butyldicarbonate
di-tertiary-butyl-dicarbonate
di-tert-butyl-dicarbonate
di(1,1-dimethylethyl) dicarbonate
di-t butyldicarbonate
di-(t-butyl) dicarbonate
bis(1,1'-dimethylethyl)dicarbonate
di t butyl dicarbonate
di(t-butoxycarbonyl)ether
di(t-butyl) dicarbonate
di-tertiary butyl dicarbonate
di-t-butyidicarbonate
(boc)2o
tert-butoxycarboxylic anhydride
ditertbutyl-dicarbonate
tert-butyl[(tert-butyl)oxycarbonyloxy]formate
di(tert-butyl)-dicarbonate
ditert.-butyl pyrocarbonate
di(-tert.butyl) dicarbonate
di-t butyl-dicarbonate
di-tert -butyl dicarbonate
di-tert-butyldicarbon-ate
pyrocarbonic acid di-t-butyl ester
di-ter-butyldicarbonate
di-ter-butyl-dicarbonate
di-tert.-butyl-dicarbonat
di-tert. butyl dicarbonate
(t-boc)2o
di-tert-butyl dicabonate
1,1-dimethylethoxycarboxylic anhydride
(di-tert-butyl)dicarbonate
t-butoxycarboxylic anhydride
di(tert.butyl) dicarbonate
di tert.butyldicarbonate
di-tertbutyldicarbonate
di-tert-butyl- dicarbonate
bis(1,1-dimethylethyl)-dicarbonate
pyrocarbonic acid-di-tert-butylester
di(tertiarybutyl) dicarbonate
di-tert.-butyl pyrocarbonate
bis(t-butoxycarbonyl)oxide
di t-butyldicarbonate
di tert-butyl dicarbonate
di-tert-buty dicarbonate
di-tert. -butyl pyrocarbonate
di-tert-butyl-dicarbonat
pyrocarbonic acid ditertiary butyl ester
DTXSID4051904
STR01939
mfcd00008805
J-520400
F0001-0830
di-tert-butyl dicarbonate, >=98.0% (gc)
C90704
CS-0017817
di-tert-butyl dicarbote
(boc)2o?boc anhydride
BCP26395
Q175718
A14905
(boc)2o boc anhydride
EN300-17516
PD118138
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
acyclic carboxylic anhydride
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (10)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (10.00)18.7374
1990's0 (0.00)18.2507
2000's3 (30.00)29.6817
2010's6 (60.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 11.91

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index11.91 (24.57)
Research Supply Index2.48 (2.92)
Research Growth Index4.40 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.91)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other11 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
hydrogen
Hydrogen: The first chemical element in the periodic table with atomic symbol H, and atomic number 1. Protium (atomic weight 1) is by far the most common hydrogen isotope. Hydrogen also exists as the stable isotope DEUTERIUM (atomic weight 2) and the radioactive isotope TRITIUM (atomic weight 3). Hydrogen forms into a diatomic molecule at room temperature and appears as a highly flammable colorless and odorless gas.. dihydrogen : An elemental molecule consisting of two hydrogens joined by a single bond.		2.0210elemental hydrogen;
elemental molecule;
gas molecular entity		antioxidant;
electron donor;
food packaging gas;
fuel;
human metabolite
trifluoroacetic acid
Trifluoroacetic Acid: A very strong halogenated derivative of acetic acid. It is used in acid catalyzed reactions, especially those where an ester is cleaved in peptide synthesis.. trifluoroacetic acid : A monocarboxylic acid that is the trifluoro derivative of acetic acid.		1.9510fluoroalkanoic acidhuman xenobiotic metabolite;
NMR chemical shift reference compound;
reagent
carbonates
Carbonates: Salts or ions of the theoretical carbonic acid, containing the radical CO2(3-). Carbonates are readily decomposed by acids. The carbonates of the alkali metals are water-soluble; all others are insoluble. (From Grant & Hackh's Chemical Dictionary, 5th ed). carbonates : Organooxygen compounds that are salts or esters of carbonic acid, H2CO3.		3.74100carbon oxoanion
ruthenium
Ruthenium: A hard, brittle, grayish-white rare earth metal with an atomic symbol Ru, atomic number 44, and atomic weight 101.07. It is used as a catalyst and hardener for PLATINUM and PALLADIUM.		2.110iron group element atom;
platinum group metal atom
quinone methide
quinone methide: intermediate in eumelanin biosynthesis; structure given in first source. quinomethane : A methylidenecyclohexadienone, formally derived from a benzoquinone by replacement of one of the quinone oxygens by a methylidene group.		2.0610quinomethane
curcudiol
curcudiol: RN given for (S)-isomer; structure in first source		2.0610
sesquiterpenes
[no description available]		2.0610
indigo carmine
Indigo Carmine: Indolesulfonic acid used as a dye in renal function testing for the detection of nitrates and chlorates, and in the testing of milk.. indigo carmine : An organic sodium salt resulting from the formal condensation of indigo carmine (acid form) with two equivalents of sodium hydroxide. It is an indicator at pH 11.5-14, changing from blue to yellow.		2.1110
tempo
TEMPO: structure. TEMPO : A member of the class of aminoxyls that is piperidine that carries an oxidanediyl group at position 1 and methyl groups at positions 2, 2, 6, and 6, respectively.		2.110aminoxyls;
piperidines		catalyst;
ferroptosis inhibitor;
radical scavenger
ConditionIndicatedRelationship StrengthStudiesTrials
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