Di-tert-butyl dicarbonate

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 Search

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

Title	Date	PubMed
tert-Butyl 4-cyano-phenyl carbonate.	2010-09-30	21587649
tert-Butyl 3-(8-bromo-4H,10H-1,2-oxazolo[4,3-c][1]benzoxepin-10-yl)-2-methyl-1H-indole-1-carboxyl-ate.	2010-07-17	21588344
Peptide-catalyzed kinetic resolution of formamides and thioformamides as an entry to nonracemic amines.	2010-03-10	20158213
Synthesis and conformational analysis of locked carbocyclic analogues of 1,3-diazepinone riboside, a high-affinity cytidine deaminase inhibitor.	2009-08-21	19618900
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.	2006-12-22	17168573
Curtius rearrangement of aromatic carboxylic acids to access protected anilines and aromatic ureas.	2006-12-07	17134255
Boronated protohaemins: synthesis and in vivo antitumour efficacy.	2006-10-21	17024289
HClO4-SiO2 as a new, highly efficient, inexpensive and reusable catalyst for N-tert-butoxycarbonylation of amines.	2006-07-21	16826301
Detection and elimination of product inhibition from the asymmetric catalytic hydrogenation of enamines.	2005-10-27	16235926
Boc-protected amines via a mild and efficient one-pot Curtius rearrangement.	2005-09-15	16146363
1,3-Alternate calix[4]arenes, selectively functionalized by amino groups.	2005-01-07	15602613
Alkylation of alkenes: ethylaluminum sesquichloride-mediated hydro-alkyl additions with alkyl chloroformates and di-tert-butylpyrocarbonate.	2004-08-25	15315446
An efficient sequence for the preparation of small secondary amine hydrochloride salts for focused library generation without need for distillation or chromatographic purification.	2004-06-21	15149663
Reactions on a solid surface. A simple, economical, and efficient acylation of alcohols and amines over Al2O3.	2004-01-23	14725479
Quantitative estimation of the degree of derivatization: an alternative methodology using 1-D and 2-D NMR experiments.	2004-01	14745821

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:20:48 GMT 2025` Edited by `admin` on `Mon Mar 31 21:20:48 GMT 2025`
Record UNII	Z10Q236C3G
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

Di-tert-butyl dicarbonate

Systematic Name

English

Boc anhydride

Preferred 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-butyloxy diformate

Systematic Name

English

Bis(tert-butoxycarbonyl)oxide

Systematic Name

English

Boc2O

Common Name

English

Code System Code Type Description

FDA UNII

Z10Q236C3G