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Details

Stereochemistry ACHIRAL
Molecular Formula C7H14O2
Molecular Weight 130.1849
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,1-DIMETHYLETHYL PROPIONATE

SMILES

CCC(=O)OC(C)(C)C

InChI

InChIKey=JAELLLITIZHOGQ-UHFFFAOYSA-N
InChI=1S/C7H14O2/c1-5-6(8)9-7(2,3)4/h5H2,1-4H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Lewis base activation of lewis acids. Addition of silyl ketene acetals to aldehydes.
2002 Nov 13
Palladium-catalyzed alpha-arylation of esters and amides under more neutral conditions.
2003 Sep 17
On the mechanism of Lewis base catalyzed aldol addition reactions: kinetic and spectroscopic investigations using rapid-injection NMR.
2009 Aug 26
Use of a robust dehydrogenase from an archael hyperthermophile in asymmetric catalysis-dynamic reductive kinetic resolution entry into (S)-profens.
2010 May 5
Patents
Name Type Language
1,1-DIMETHYLETHYL PROPIONATE
Systematic Name English
PROPANOIC ACID, 1,1-DIMETHYLETHYL ESTER
Common Name English
Code System Code Type Description
CAS
20487-40-5
Created by admin on Sat Dec 16 09:35:19 GMT 2023 , Edited by admin on Sat Dec 16 09:35:19 GMT 2023
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PUBCHEM
88561
Created by admin on Sat Dec 16 09:35:19 GMT 2023 , Edited by admin on Sat Dec 16 09:35:19 GMT 2023
PRIMARY
EPA CompTox
DTXSID20174459
Created by admin on Sat Dec 16 09:35:19 GMT 2023 , Edited by admin on Sat Dec 16 09:35:19 GMT 2023
PRIMARY
FDA UNII
43953CC10D
Created by admin on Sat Dec 16 09:35:19 GMT 2023 , Edited by admin on Sat Dec 16 09:35:19 GMT 2023
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