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Details

Stereochemistry RACEMIC
Molecular Formula C6H12O3
Molecular Weight 132.1577
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SOLKETAL

SMILES

CC1(C)OCC(CO)O1

InChI

InChIKey=RNVYQYLELCKWAN-UHFFFAOYSA-N
InChI=1S/C6H12O3/c1-6(2)8-4-5(3-7)9-6/h5,7H,3-4H2,1-2H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Membrane plasmalogen composition and cellular cholesterol regulation: a structure activity study.
2010-06-14
(2,2-Dimethyl-1,3-dioxolan-4-yl)methyl 3-carboxy-propanoate.
2009-05-07
2,3-O-Isopropyl-idene-1-O-p-tolyl-sulfonylglycerol.
2009-05-07
A genetic selection system for evolving enantioselectivity of enzymes.
2008-11-21
Photocytotoxicity of mTHPC (temoporfin) loaded polymeric micelles mediated by lipase catalyzed degradation.
2008-09
A novel genetic selection system for improved enantioselectivity of Bacillus subtilis lipase A.
2008-05-05
Purification and characterization of the enantioselective esterase from Kluyveromyces marxianus CBS 1553.
2008-01-01
Cardiovascular effects of selected water-miscible solvents for pharmaceutical injections and embolization materials: a comparative hemodynamic study using a sheep model.
2007-05-08
Peripheral and axial substitution of phthalocyanines with solketal groups: synthesis and in vitro evaluation for photodynamic therapy.
2007-04-05
Fourier transform near-infrared vibrational circular dichroism used for on-line monitoring the epimerization of 2,2-dimethyl-1,3-dioxolane-4-methanol: A pseudo racemization reaction.
2006-11
Organic solvents as vehicles for precipitating liquid embolics: a comparative angiotoxicity study with superselective injections of swine rete mirabile.
2006-10
Practical enantiospecific syntheses of lysobisphosphatidic acid and its analogues.
2006-02-03
Synthesis of acyclic analogs of adenosine.
2005-10
Racemic and optically active 2-methoxy-4-oxatetradecanoic acids: novel synthetic fatty acids with selective antifungal properties.
2005-07
Enhancement of enzyme activity and enantioselectivity by cyclopentyl methyl ether in the transesterification catalyzed by Pseudomonas cepacia lipase co-lyophilized with cyclodextrins.
2005-03
Newly isolated Streptomyces spp. as enantioselective biocatalysts: hydrolysis of 1,2-O-isopropylidene glycerol racemic esters.
2005
Extension of fourier transform vibrational circular dichroism into the near-infrared region: continuous spectral coverage from 800 to 10 000 cm(-1).
2004-09
Stereochemistry of a diastereoisomeric amphiphile and the species of the lipase influence enzyme activity in the transesterification catalyzed by a lipase-co-lyophilizate with the amphiphile in organic media.
2003-11
Deuterium isotope effect on enantioselectivity in the Comamonas testosteroni quinohemoprotein alcohol dehydrogenase-catalyzed kinetic resolution of rac-2,2-dimethyl-4-hydroxymethyl-1,3-dioxolane, solketal.
2003-04-11
Novel trifluoromethyl ketones as potent gastric lipase inhibitors.
2003-01-03
Enhanced enzyme activity and enantioselectivity of lipases in organic solvents by crown ethers and cyclodextrins.
2003
Facile synthesis of plasmalogens via Barbier-type reactions of vinyl dioxanes and vinyl dioxolanes with alkyl halides in LiDBB solution.
2002-09-06
In vitro toxicities of experimental jet fuel system ice-inhibiting agents.
2001-07-02
Comparative hemolytic activity of undiluted organic water-miscible solvents for intravenous and intra-arterial injection.
2001-02-24
2-Hydroxymethyl-1,4-dioxane: synthesis, resolution and determination of the absolute configurations of the enantiomers.
2001
Patents
Name Type Language
ISOPROPYLIDENE GLYCEROL
MI  
Preferred Name English
SOLKETAL
Common Name English
GLYCEROL ACETONIDE
Systematic Name English
ISOPROPYLIDENE GLYCEROL [MI]
Common Name English
ACETONE GLYCERIN KETAL
Common Name English
2,2-DIMETHYL-1,3-DIOXOLANE-4-METHANOL
Systematic Name English
GLYCEROL DIMETHYLKETAL
Common Name English
NSC-59720
Code English
2,3-ISOPROPYLIDENEGLYCEROL
Common Name English
Classification Tree Code System Code
Food Contact Sustance Notif, (FCN No.) FCN NO. 1149
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
Code System Code Type Description
FDA UNII
3XK098O8ZW
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
SMS_ID
100000092830
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
EPA CompTox
DTXSID9021845
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
CAS
100-79-8
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
DAILYMED
3XK098O8ZW
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
RXCUI
2180790
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-888-7
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
MESH
C024356
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
EVMPD
SUB29281
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
PUBCHEM
7528
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
MERCK INDEX
m6529
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY Merck Index
WIKIPEDIA
SOLKETAL
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY
NSC
59720
Created by admin on Mon Mar 31 17:55:27 GMT 2025 , Edited by admin on Mon Mar 31 17:55:27 GMT 2025
PRIMARY