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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

Molecular Formula C6H12O3
Molecular Weight 132.1577
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Enhanced enzyme activity and enantioselectivity of lipases in organic solvents by crown ethers and cyclodextrins.
2003
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 Apr 11
Novel trifluoromethyl ketones as potent gastric lipase inhibitors.
2003 Jan 3
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 Nov
Extension of fourier transform vibrational circular dichroism into the near-infrared region: continuous spectral coverage from 800 to 10 000 cm(-1).
2004 Sep
Newly isolated Streptomyces spp. as enantioselective biocatalysts: hydrolysis of 1,2-O-isopropylidene glycerol racemic esters.
2005
Racemic and optically active 2-methoxy-4-oxatetradecanoic acids: novel synthetic fatty acids with selective antifungal properties.
2005 Jul
Enhancement of enzyme activity and enantioselectivity by cyclopentyl methyl ether in the transesterification catalyzed by Pseudomonas cepacia lipase co-lyophilized with cyclodextrins.
2005 Mar
Synthesis of acyclic analogs of adenosine.
2005 Oct
Practical enantiospecific syntheses of lysobisphosphatidic acid and its analogues.
2006 Feb 3
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 Nov
Organic solvents as vehicles for precipitating liquid embolics: a comparative angiotoxicity study with superselective injections of swine rete mirabile.
2006 Oct
Peripheral and axial substitution of phthalocyanines with solketal groups: synthesis and in vitro evaluation for photodynamic therapy.
2007 Apr 5
Cardiovascular effects of selected water-miscible solvents for pharmaceutical injections and embolization materials: a comparative hemodynamic study using a sheep model.
2007 Mar-Apr
Purification and characterization of the enantioselective esterase from Kluyveromyces marxianus CBS 1553.
2008 Jan 1
A novel genetic selection system for improved enantioselectivity of Bacillus subtilis lipase A.
2008 May 5
A genetic selection system for evolving enantioselectivity of enzymes.
2008 Nov 21
Photocytotoxicity of mTHPC (temoporfin) loaded polymeric micelles mediated by lipase catalyzed degradation.
2008 Sep
(2,2-Dimethyl-1,3-dioxolan-4-yl)methyl 3-carboxy-propanoate.
2009 May 7
2,3-O-Isopropyl-idene-1-O-p-tolyl-sulfonylglycerol.
2009 May 7
Membrane plasmalogen composition and cellular cholesterol regulation: a structure activity study.
2010 Jun 14
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:22:12 UTC 2023
Edited
by admin
on Fri Dec 15 15:22:12 UTC 2023
Record UNII
3XK098O8ZW
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SOLKETAL
Common Name English
ISOPROPYLIDENE GLYCEROL
MI  
Systematic 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 Fri Dec 15 15:22:12 UTC 2023 , Edited by admin on Fri Dec 15 15:22:12 UTC 2023
Code System Code Type Description
FDA UNII
3XK098O8ZW
Created by admin on Fri Dec 15 15:22:12 UTC 2023 , Edited by admin on Fri Dec 15 15:22:12 UTC 2023
PRIMARY
SMS_ID
100000092830
Created by admin on Fri Dec 15 15:22:12 UTC 2023 , Edited by admin on Fri Dec 15 15:22:12 UTC 2023
PRIMARY
EPA CompTox
DTXSID9021845
Created by admin on Fri Dec 15 15:22:12 UTC 2023 , Edited by admin on Fri Dec 15 15:22:12 UTC 2023
PRIMARY
CAS
100-79-8
Created by admin on Fri Dec 15 15:22:12 UTC 2023 , Edited by admin on Fri Dec 15 15:22:12 UTC 2023
PRIMARY
DAILYMED
3XK098O8ZW
Created by admin on Fri Dec 15 15:22:12 UTC 2023 , Edited by admin on Fri Dec 15 15:22:12 UTC 2023
PRIMARY
RXCUI
2180790
Created by admin on Fri Dec 15 15:22:12 UTC 2023 , Edited by admin on Fri Dec 15 15:22:12 UTC 2023
PRIMARY
ECHA (EC/EINECS)
202-888-7
Created by admin on Fri Dec 15 15:22:12 UTC 2023 , Edited by admin on Fri Dec 15 15:22:12 UTC 2023
PRIMARY
MESH
C024356
Created by admin on Fri Dec 15 15:22:12 UTC 2023 , Edited by admin on Fri Dec 15 15:22:12 UTC 2023
PRIMARY
EVMPD
SUB29281
Created by admin on Fri Dec 15 15:22:12 UTC 2023 , Edited by admin on Fri Dec 15 15:22:12 UTC 2023
PRIMARY
PUBCHEM
7528
Created by admin on Fri Dec 15 15:22:12 UTC 2023 , Edited by admin on Fri Dec 15 15:22:12 UTC 2023
PRIMARY
MERCK INDEX
m6529
Created by admin on Fri Dec 15 15:22:12 UTC 2023 , Edited by admin on Fri Dec 15 15:22:12 UTC 2023
PRIMARY Merck Index
WIKIPEDIA
SOLKETAL
Created by admin on Fri Dec 15 15:22:12 UTC 2023 , Edited by admin on Fri Dec 15 15:22:12 UTC 2023
PRIMARY
NSC
59720
Created by admin on Fri Dec 15 15:22:12 UTC 2023 , Edited by admin on Fri Dec 15 15:22:12 UTC 2023
PRIMARY