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Details

Stereochemistry ACHIRAL
Molecular Formula C3H7NO2
Molecular Weight 89.0932
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-NITROPROPANE

SMILES

CCC[N+]([O-])=O

InChI

InChIKey=JSZOAYXJRCEYSX-UHFFFAOYSA-N
InChI=1S/C3H7NO2/c1-2-3-4(5)6/h2-3H2,1H3

HIDE SMILES / InChI

Molecular Formula C3H7NO2
Molecular Weight 89.0932
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Discrimination of carcinogens by hepatic transcript profiling in rats following 28-day administration.
2009-11-13
Thermodynamic consistency near the liquid-liquid critical point.
2009-01-28
(2,4-Dinitro-phen-yl)(1-methyl-1-nitro-ethyl)diazene.
2008-10-25
Solubilization of an organic solute in aqueous solutions of unimeric block copolymers and their mixtures with monomeric surfactant: volume, surface tension, differential scanning calorimetry, viscosity, and fluorescence spectroscopy studies.
2008-05-08
Differences in gene expression profiles in the liver between carcinogenic and non-carcinogenic isomers of compounds given to rats in a 28-day repeat-dose toxicity study.
2006-12-15
Inter- and intramolecular glycosylation of exo-glycals promoted by metallic Lewis acids.
2006-07-24
Gibbs energies of transfer of alkali metal cations between mutually saturated water-solvent systems determined from extraction experiments with radiotracer 137Cs.
2006-04-27
Stereochemical memory effects in alkene radical cation/anion contact ion pairs: effect of substituents, and models for diastereoselectivity.
2005-07-13
Scope and limitations of the nitro-Mannich reaction for the stereoselective synthesis of 1,2-diamines.
2005-01-21
Highly enantioselective conjugate addition of nitroalkanes to alkylidenemalonates using efficient phase-transfer catalysis of N-spiro chiral ammonium bromides.
2004-09-29
The McLafferty rearrangement: a personal recollection.
2004-07
Spin trapping of nitric oxide by aci anions of nitroalkanes.
2004-03
An efficient nitration of light alkanes and the alkyl side-chain of aromatic compounds with nitrogen dioxide and nitric acid catalyzed by N-hydroxyphthalimide.
2002-08-09
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:42:06 GMT 2025
Edited
by admin
on Mon Mar 31 18:42:06 GMT 2025
Record UNII
39W305OW99
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1-NITROPROPANE
HSDB   MI  
Systematic Name English
NSC-6363
Preferred Name English
1-NITROPROPANE [MI]
Common Name English
1-NITROPROPANE [HSDB]
Common Name English
NITROPROPANE, 1-
Systematic Name English
Code System Code Type Description
MERCK INDEX
m7984
Created by admin on Mon Mar 31 18:42:06 GMT 2025 , Edited by admin on Mon Mar 31 18:42:06 GMT 2025
PRIMARY Merck Index
MESH
C035314
Created by admin on Mon Mar 31 18:42:06 GMT 2025 , Edited by admin on Mon Mar 31 18:42:06 GMT 2025
PRIMARY
FDA UNII
39W305OW99
Created by admin on Mon Mar 31 18:42:06 GMT 2025 , Edited by admin on Mon Mar 31 18:42:06 GMT 2025
PRIMARY
EPA CompTox
DTXSID1020980
Created by admin on Mon Mar 31 18:42:06 GMT 2025 , Edited by admin on Mon Mar 31 18:42:06 GMT 2025
PRIMARY
NSC
6363
Created by admin on Mon Mar 31 18:42:06 GMT 2025 , Edited by admin on Mon Mar 31 18:42:06 GMT 2025
PRIMARY
PUBCHEM
7903
Created by admin on Mon Mar 31 18:42:06 GMT 2025 , Edited by admin on Mon Mar 31 18:42:06 GMT 2025
PRIMARY
CHEBI
76261
Created by admin on Mon Mar 31 18:42:06 GMT 2025 , Edited by admin on Mon Mar 31 18:42:06 GMT 2025
PRIMARY
HSDB
2526
Created by admin on Mon Mar 31 18:42:06 GMT 2025 , Edited by admin on Mon Mar 31 18:42:06 GMT 2025
PRIMARY
CAS
108-03-2
Created by admin on Mon Mar 31 18:42:06 GMT 2025 , Edited by admin on Mon Mar 31 18:42:06 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-544-9
Created by admin on Mon Mar 31 18:42:06 GMT 2025 , Edited by admin on Mon Mar 31 18:42:06 GMT 2025
PRIMARY
WIKIPEDIA
1-Nitropropane
Created by admin on Mon Mar 31 18:42:06 GMT 2025 , Edited by admin on Mon Mar 31 18:42:06 GMT 2025
PRIMARY