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Details

Stereochemistry ACHIRAL
Molecular Formula C6H12O2
Molecular Weight 116.1583
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TERT-BUTYL ACETATE

SMILES

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

InChI

InChIKey=WMOVHXAZOJBABW-UHFFFAOYSA-N
InChI=1S/C6H12O2/c1-5(7)8-6(2,3)4/h1-4H3

HIDE SMILES / InChI

Molecular Formula C6H12O2
Molecular Weight 116.1583
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Induction of CYP3A4 by 1 alpha,25-dihydroxyvitamin D3 is human cell line-specific and is unlikely to involve pregnane X receptor.
2001 Nov
Polymorphic behavior of an NK1 receptor antagonist.
2002 Aug 28
Tailoring fatty food simulants made from solvent mixtures (2): determining the equivalent migration behaviour of olive oil and of solvents in the case of polyolefins.
2002 Jun
Antimicrobial and bactericidal activities of esters of 2-endo-hydroxy-1,8-cineole as new aroma chemicals.
2002 Jun 5
Fluorogenic stereochemical probes for transaldolases.
2003 Feb 17
Palladium-catalyzed alpha-arylation of esters and amides under more neutral conditions.
2003 Sep 17
Interfacial reactions in confinement: kinetics and temperature dependence of the surface hydrolysis of polystyrene-block-poly(tert-butyl acrylate) thin films.
2005 Mar 15
Synthesis of 2H-1,2-benzothiazine 1,1-dioxides via heteroannulation reactions of 2-iodobenzenesulfonamide with ketone enolates under S(RN)1 conditions.
2005 Nov 11
Asymmetric synthesis of orthogonally protected trans-cyclopropane gamma-amino acids via intramolecular ring closure.
2006 Aug 21
Effects of tert-butyl acetate on maternal toxicity and embryo-fetal development in Sprague-Dawley rats.
2007 Oct
Palladium-catalyzed alpha-arylation of esters with chloroarenes.
2008 Apr 17
Amphiphilic hyperbranched fluoropolymers as nanoscopic 19F magnetic resonance imaging agent assemblies.
2008 Oct
An efficient and scalable Ritter reaction for the synthesis of tert-butyl amides.
2009 Mar 6
[H2O2 oxidation of 1,4-dihydropyridines over Mg2+ ion exchanged clinoptilolite and solventless solid state acid decomposition of ester to 3,5-pyridinedicarboxylic acid].
2009 Oct
Iridium-catalyzed alpha-alkylation of acetates with primary alcohols and diols.
2010 Mar 3
Nucleophilic addition to 2,3-disubstituted butanal derivatives and their application to natural product synthesis.
2010 Oct
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:50:43 GMT 2023
Edited
by admin
on Fri Dec 15 17:50:43 GMT 2023
Record UNII
76N22HKP3X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TERT-BUTYL ACETATE
HSDB   MI  
Systematic Name English
BUTYL ACETATE, TERT-
Systematic Name English
TERT-BUTYL ACETATE [HSDB]
Common Name English
T-BUTYL ACETATE
INCI  
INCI  
Official Name English
T-BUTYL ACETATE [INCI]
Common Name English
NSC-59719
Code English
TERT-BUTYL ACETATE [MI]
Common Name English
Code System Code Type Description
PUBCHEM
10908
Created by admin on Fri Dec 15 17:50:43 GMT 2023 , Edited by admin on Fri Dec 15 17:50:43 GMT 2023
PRIMARY
MERCK INDEX
m2809
Created by admin on Fri Dec 15 17:50:43 GMT 2023 , Edited by admin on Fri Dec 15 17:50:43 GMT 2023
PRIMARY Merck Index
FDA UNII
76N22HKP3X
Created by admin on Fri Dec 15 17:50:43 GMT 2023 , Edited by admin on Fri Dec 15 17:50:43 GMT 2023
PRIMARY
EPA CompTox
DTXSID1022055
Created by admin on Fri Dec 15 17:50:43 GMT 2023 , Edited by admin on Fri Dec 15 17:50:43 GMT 2023
PRIMARY
NSC
59719
Created by admin on Fri Dec 15 17:50:43 GMT 2023 , Edited by admin on Fri Dec 15 17:50:43 GMT 2023
PRIMARY
CAS
540-88-5
Created by admin on Fri Dec 15 17:50:43 GMT 2023 , Edited by admin on Fri Dec 15 17:50:43 GMT 2023
PRIMARY
WIKIPEDIA
TERT-BUTYL ACETATE
Created by admin on Fri Dec 15 17:50:43 GMT 2023 , Edited by admin on Fri Dec 15 17:50:43 GMT 2023
PRIMARY
ECHA (EC/EINECS)
208-760-7
Created by admin on Fri Dec 15 17:50:43 GMT 2023 , Edited by admin on Fri Dec 15 17:50:43 GMT 2023
PRIMARY
MESH
C089834
Created by admin on Fri Dec 15 17:50:43 GMT 2023 , Edited by admin on Fri Dec 15 17:50:43 GMT 2023
PRIMARY
HSDB
835
Created by admin on Fri Dec 15 17:50:43 GMT 2023 , Edited by admin on Fri Dec 15 17:50:43 GMT 2023
PRIMARY