SOLKETAL

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 Search

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

Title	Date	PubMed
2-Hydroxymethyl-1,4-dioxane: synthesis, resolution and determination of the absolute configurations of the enantiomers.	2001	11762921
Comparative hemolytic activity of undiluted organic water-miscible solvents for intravenous and intra-arterial injection.	2001 Jan-Feb	11212416
In vitro toxicities of experimental jet fuel system ice-inhibiting agents.	2001 Jul 2	11453297
Facile synthesis of plasmalogens via Barbier-type reactions of vinyl dioxanes and vinyl dioxolanes with alkyl halides in LiDBB solution.	2002 Sep 6	12201773
Enhanced enzyme activity and enantioselectivity of lipases in organic solvents by crown ethers and cyclodextrins.	2003	16233437
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	12686148
Novel trifluoromethyl ketones as potent gastric lipase inhibitors.	2003 Jan 3	12512081
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	14677713
Extension of fourier transform vibrational circular dichroism into the near-infrared region: continuous spectral coverage from 800 to 10 000 cm(-1).	2004 Sep	15479522
Newly isolated Streptomyces spp. as enantioselective biocatalysts: hydrolysis of 1,2-O-isopropylidene glycerol racemic esters.	2005	16162249
Racemic and optically active 2-methoxy-4-oxatetradecanoic acids: novel synthetic fatty acids with selective antifungal properties.	2005 Jul	15899476
Enhancement of enzyme activity and enantioselectivity by cyclopentyl methyl ether in the transesterification catalyzed by Pseudomonas cepacia lipase co-lyophilized with cyclodextrins.	2005 Mar	15834802
Synthesis of acyclic analogs of adenosine.	2005 Oct	18428937
Practical enantiospecific syntheses of lysobisphosphatidic acid and its analogues.	2006 Feb 3	16438504
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	16906494
Organic solvents as vehicles for precipitating liquid embolics: a comparative angiotoxicity study with superselective injections of swine rete mirabile.	2006 Oct	17032862
Photocytotoxicity of mTHPC (temoporfin) loaded polymeric micelles mediated by lipase catalyzed degradation.	2008 Sep	18597164
(2,2-Dimethyl-1,3-dioxolan-4-yl)methyl 3-carboxy-propanoate.	2009 May 7	21583064
2,3-O-Isopropyl-idene-1-O-p-tolyl-sulfonylglycerol.	2009 May 7	21583063

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 15:22:12 GMT 2023` Edited by `admin` on `Fri Dec 15 15:22:12 GMT 2023`
Record UNII	3XK098O8ZW
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

SOLKETAL

Common Name

English

ISOPROPYLIDENE GLYCEROL

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