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Details

Stereochemistry ACHIRAL
Molecular Formula C5H12O2
Molecular Weight 104.1476
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,2-Dimethoxypropane

SMILES

COC(C)(C)OC

InChI

InChIKey=HEWZVZIVELJPQZ-UHFFFAOYSA-N
InChI=1S/C5H12O2/c1-5(2,6-3)7-4/h1-4H3

HIDE SMILES / InChI

Molecular Formula C5H12O2
Molecular Weight 104.1476
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Acetonation of L-pentoses and 6-deoxy-L-hexoses under kinetic control using heterogeneous acid catalysts.
2010-07-19
Mobilization of lipid reserves during germination of oat (Avena sativa L.), a cereal rich in endosperm oil.
2010-06
Barium Titanate Nanoparticles: Highly Cytocompatible Dispersions in Glycol-chitosan and Doxorubicin Complexes for Cancer Therapy.
2010-05-09
Determination of dimethyl sulfoxide and dimethyl sulfone in urine by gas chromatography-mass spectrometry after preparation using 2,2-dimethoxypropane.
2010-05
Investigation of interactions between poly-L-lysine-coated boron nitride nanotubes and C2C12 cells: up-take, cytocompatibility, and differentiation.
2010-04-15
Inhibition of Escherichia coli glycosyltransferase MurG and Mycobacterium tuberculosis Gal transferase by uridine-linked transition state mimics.
2010-04-01
A simple and convenient synthetic protocol for O-isopropylidenation of sugars using bromodimethylsulfonium bromide (BDMS) as a catalyst.
2010-01-11
Preparation and synthetic application of partially protected brassinosteroids.
2010-01
Hydrogen-Bonded Networks Based on Cobalt(II), Nickel(II), and Zinc(II) Complexes of N,N'-Diethylurea.
2010
Isolation of C11 cyclopentenones from two didemnid species, Lissoclinum sp. and Diplosoma sp.
2009-12-17
Specialized ommatidia of the polarization-sensitive dorsal rim area in the eye of monarch butterflies have non-functional reflecting tapeta.
2009-12
Redetermination of methyl 3,4-O-isopropyl-idene-β-D-fucopyran-oside monohydrate.
2009-04-08
Synthesis of bicyclo[5.3.0]azulene derivatives.
2009
Natural products as an inspiration in the diversity-oriented synthesis of bioactive compound libraries.
2008-08
2,10-Dibromo-6,6-dimethyl-dibenzo[d,f][1,3]dioxepine.
2008-03-20
Attainment of brown adipocyte features in white adipocytes of hormone-sensitive lipase null mice.
2008-03-12
An efficient synthesis of quinoxaline derivatives from 4-chloro-4-deoxy-alpha-D-galactose and their cytotoxic activities.
2007-02-01
Polyketal microparticles: a new delivery vehicle for superoxide dismutase.
2007-01-18
Investigation of acetyl migrations in furanosides.
2006-07-21
An efficient synthesis of methyl 1,3-O-isopropylidene-alpha-D-fructofuranoside and 2,3:5,6-di-O-isopropylidene-D-glucose dimethyl acetal derivatives from sucrose.
2005-11-21
Quantitative determination of moisture in lubricants by Fourier transform infrared spectroscopy.
2004-02
Decomposition of 2-bromophenol in NaOH solution at high temperature.
2003-08-01
Matrix isolation infrared and ab initio study of the conformations of 2,2-dimethoxypropane.
2003-05
Preparation of serial sections of arthropods using 2,2-dimethoxypropane dehydration and epoxy resin embedding under vacuum.
2003-02
Mixed acetals of cyclodextrins. Preparation of hexakis-, heptakis- and octakis[2,6-di-O-(methoxydimethyl)methyl]-alpha-, beta- and gamma-cyclodextrins.
2002-02-05
Effects of phosphoprotein phosphatase inhibitors (phenylarsine oxide and cantharidin) on Tetrahymena.
2001-09
Improved procedure for the analysis of gamma-hydroxybutyrate and ethylene glycol in whole blood.
2001-08-14
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:05:25 GMT 2025
Edited
by admin
on Mon Mar 31 21:05:25 GMT 2025
Record UNII
66P41R0030
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,2-Dimethoxypropane
Systematic Name English
NSC-62085
Preferred Name English
ACETONE DIMETHYL KETAL
Systematic Name English
PROPANE, 2,2-DIMETHOXY-
Systematic Name English
Code System Code Type Description
WIKIPEDIA
2,2-DIMETHOXYPROPANE
Created by admin on Mon Mar 31 21:05:25 GMT 2025 , Edited by admin on Mon Mar 31 21:05:25 GMT 2025
PRIMARY
CAS
77-76-9
Created by admin on Mon Mar 31 21:05:25 GMT 2025 , Edited by admin on Mon Mar 31 21:05:25 GMT 2025
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MESH
C017240
Created by admin on Mon Mar 31 21:05:25 GMT 2025 , Edited by admin on Mon Mar 31 21:05:25 GMT 2025
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NSC
62085
Created by admin on Mon Mar 31 21:05:25 GMT 2025 , Edited by admin on Mon Mar 31 21:05:25 GMT 2025
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PUBCHEM
6495
Created by admin on Mon Mar 31 21:05:25 GMT 2025 , Edited by admin on Mon Mar 31 21:05:25 GMT 2025
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EPA CompTox
DTXSID7026441
Created by admin on Mon Mar 31 21:05:25 GMT 2025 , Edited by admin on Mon Mar 31 21:05:25 GMT 2025
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ECHA (EC/EINECS)
201-056-0
Created by admin on Mon Mar 31 21:05:25 GMT 2025 , Edited by admin on Mon Mar 31 21:05:25 GMT 2025
PRIMARY
FDA UNII
66P41R0030
Created by admin on Mon Mar 31 21:05:25 GMT 2025 , Edited by admin on Mon Mar 31 21:05:25 GMT 2025
PRIMARY