U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C10H18O5
Molecular Weight 218.2469
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DI-TERT-BUTYL DICARBONATE

SMILES

CC(C)(C)OC(=O)OC(=O)OC(C)(C)C

InChI

InChIKey=DYHSDKLCOJIUFX-UHFFFAOYSA-N
InChI=1S/C10H18O5/c1-9(2,3)14-7(11)13-8(12)15-10(4,5)6/h1-6H3

HIDE SMILES / InChI

Molecular Formula C10H18O5
Molecular Weight 218.2469
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Alkylation of alkenes: ethylaluminum sesquichloride-mediated hydro-alkyl additions with alkyl chloroformates and di-tert-butylpyrocarbonate.
2004 Aug 25
Quantitative estimation of the degree of derivatization: an alternative methodology using 1-D and 2-D NMR experiments.
2004 Jan
Reactions on a solid surface. A simple, economical, and efficient acylation of alcohols and amines over Al2O3.
2004 Jan 23
An efficient sequence for the preparation of small secondary amine hydrochloride salts for focused library generation without need for distillation or chromatographic purification.
2004 Jun 21
1,3-Alternate calix[4]arenes, selectively functionalized by amino groups.
2005 Jan 7
Detection and elimination of product inhibition from the asymmetric catalytic hydrogenation of enamines.
2005 Oct 27
Boc-protected amines via a mild and efficient one-pot Curtius rearrangement.
2005 Sep 15
Alcohols and di-tert-butyl dicarbonate: how the nature of the Lewis acid catalyst may address the reaction to the synthesis of tert-butyl ethers.
2006 Dec 22
Curtius rearrangement of aromatic carboxylic acids to access protected anilines and aromatic ureas.
2006 Dec 7
HClO4-SiO2 as a new, highly efficient, inexpensive and reusable catalyst for N-tert-butoxycarbonylation of amines.
2006 Jul 21
Boronated protohaemins: synthesis and in vivo antitumour efficacy.
2006 Oct 21
Synthesis and conformational analysis of locked carbocyclic analogues of 1,3-diazepinone riboside, a high-affinity cytidine deaminase inhibitor.
2009 Aug 21
tert-Butyl 3-(8-bromo-4H,10H-1,2-oxazolo[4,3-c][1]benzoxepin-10-yl)-2-methyl-1H-indole-1-carboxyl-ate.
2010 Jul 17
Peptide-catalyzed kinetic resolution of formamides and thioformamides as an entry to nonracemic amines.
2010 Mar 10
tert-Butyl 4-cyano-phenyl carbonate.
2010 Sep 30
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 04:02:29 UTC 2023
Edited
by admin
on Sat Dec 16 04:02:29 UTC 2023
Record UNII
Z10Q236C3G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DI-TERT-BUTYL DICARBONATE
MI  
Systematic Name English
DICARBONIC ACID C,C'-BIS(1,1-DIMETHYLETHYL) ESTER
Common Name English
DI-TERT-BUTYL PYROCARBONATE
Systematic Name English
DI-TERT-BUTYL DICARBONATE [MI]
Common Name English
DICARBONIC ACID, BIS(1,1-DIMETHYLETHYL) ESTER
Common Name English
DI-TERT-BUTYL OXYDIFORMATE
Systematic Name English
BIS(TERT-BUTOXYCARBONYL)OXIDE
Systematic Name English
BOC2O
Common Name English
BOC ANHYDRIDE
Common Name English
Code System Code Type Description
FDA UNII
Z10Q236C3G
Created by admin on Sat Dec 16 04:02:29 UTC 2023 , Edited by admin on Sat Dec 16 04:02:29 UTC 2023
PRIMARY
PUBCHEM
90495
Created by admin on Sat Dec 16 04:02:29 UTC 2023 , Edited by admin on Sat Dec 16 04:02:29 UTC 2023
PRIMARY
ECHA (EC/EINECS)
246-240-1
Created by admin on Sat Dec 16 04:02:29 UTC 2023 , Edited by admin on Sat Dec 16 04:02:29 UTC 2023
PRIMARY
WIKIPEDIA
DI-TERT-BUTYL DICARBONATE
Created by admin on Sat Dec 16 04:02:29 UTC 2023 , Edited by admin on Sat Dec 16 04:02:29 UTC 2023
PRIMARY
EPA CompTox
DTXSID4051904
Created by admin on Sat Dec 16 04:02:29 UTC 2023 , Edited by admin on Sat Dec 16 04:02:29 UTC 2023
PRIMARY
MERCK INDEX
m4308
Created by admin on Sat Dec 16 04:02:29 UTC 2023 , Edited by admin on Sat Dec 16 04:02:29 UTC 2023
PRIMARY Merck Index
CHEBI
48500
Created by admin on Sat Dec 16 04:02:29 UTC 2023 , Edited by admin on Sat Dec 16 04:02:29 UTC 2023
PRIMARY
CAS
24424-99-5
Created by admin on Sat Dec 16 04:02:29 UTC 2023 , Edited by admin on Sat Dec 16 04:02:29 UTC 2023
PRIMARY