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Details

Stereochemistry ACHIRAL
Molecular Formula C7H16
Molecular Weight 100.2019
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,4-DIMETHYLPENTANE

SMILES

CC(C)CC(C)C

InChI

InChIKey=BZHMBWZPUJHVEE-UHFFFAOYSA-N
InChI=1S/C7H16/c1-6(2)5-7(3)4/h6-7H,5H2,1-4H3

HIDE SMILES / InChI

Molecular Formula C7H16
Molecular Weight 100.2019
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Isopropylamino and isobutylamino groups as recognition sites for carbohydrates: acyclic receptors with enhanced binding affinity toward β-galactosides.
2010-10-01
Study of the soret effect in hydrocarbon chain/aromatic compound mixtures.
2009-10-08
Reverse nonequilibrium molecular dynamics calculation of the Soret coefficient in liquid heptane/benzene mixtures.
2008-11-27
Release of volatile organic compounds (VOCs) from the lung cancer cell line CALU-1 in vitro.
2008-11-24
Surface tensions of linear and branched alkanes from Monte Carlo simulations using the anisotropic united atom model.
2008-11-06
Structural analysis of urate oxidase in complex with its natural substrate inhibited by cyanide: mechanistic implications.
2008-07-20
Biodegradability of alkylates as a sole carbon source in the presence of ethanol or BTEX.
2007-06
Alpha,omega-functionalized 2,4-dimethylpentane dyads and 2,4,6-trimethylheptane triads through asymmetric hydrogenation.
2007
Study of the thermal diffusion behavior of alkane/benzene mixtures by thermal diffusion forced rayleigh scattering experiments and lattice model calculations.
2006-12-28
Measurement and estimation of rate constants for the reactions of hydroxyl radical with several alkanes and cycloalkanes.
2006-03-16
Sterically-controlled regioselective para-substitutions of aniline.
2005-08-14
EPR and modelling studies of hydrogen-abstraction reactions relevant to polyolefin cross-linking and grafting chemistry.
2003-04-07
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:07:53 GMT 2025
Edited
by admin
on Mon Mar 31 19:07:53 GMT 2025
Record UNII
4JT8Q9QOHI
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,4-DIMETHYLPENTANE
Systematic Name English
NSC-61989
Preferred Name English
PENTANE, 2,4-DIMETHYL-
Systematic Name English
Code System Code Type Description
WIKIPEDIA
2,4-Dimethylpentane
Created by admin on Mon Mar 31 19:07:53 GMT 2025 , Edited by admin on Mon Mar 31 19:07:53 GMT 2025
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MESH
C068571
Created by admin on Mon Mar 31 19:07:53 GMT 2025 , Edited by admin on Mon Mar 31 19:07:53 GMT 2025
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NSC
61989
Created by admin on Mon Mar 31 19:07:53 GMT 2025 , Edited by admin on Mon Mar 31 19:07:53 GMT 2025
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ECHA (EC/EINECS)
203-548-0
Created by admin on Mon Mar 31 19:07:53 GMT 2025 , Edited by admin on Mon Mar 31 19:07:53 GMT 2025
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FDA UNII
4JT8Q9QOHI
Created by admin on Mon Mar 31 19:07:53 GMT 2025 , Edited by admin on Mon Mar 31 19:07:53 GMT 2025
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PUBCHEM
7907
Created by admin on Mon Mar 31 19:07:53 GMT 2025 , Edited by admin on Mon Mar 31 19:07:53 GMT 2025
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CAS
108-08-7
Created by admin on Mon Mar 31 19:07:53 GMT 2025 , Edited by admin on Mon Mar 31 19:07:53 GMT 2025
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EPA CompTox
DTXSID2059358
Created by admin on Mon Mar 31 19:07:53 GMT 2025 , Edited by admin on Mon Mar 31 19:07:53 GMT 2025
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