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Details

Stereochemistry ACHIRAL
Molecular Formula C3H6O2
Molecular Weight 74.0785
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Ethyl formate

SMILES

CCOC=O

InChI

InChIKey=WBJINCZRORDGAQ-UHFFFAOYSA-N
InChI=1S/C3H6O2/c1-2-5-3-4/h3H,2H2,1H3

HIDE SMILES / InChI

Molecular Formula C3H6O2
Molecular Weight 74.0785
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Materials for pharmaceutical dosage forms: molecular pharmaceutics and controlled release drug delivery aspects.
2010-09-15
Enzymatic dynamic kinetic resolution of (+/-)-cis-N-(alkoxycarbonyl)cyclopentane-1,2-diamines based on spontaneous racemization.
2010-08-20
Selected ion flow tube-mass spectrometry for absolute quantification of aroma compounds in the headspace of dry fermented sausages.
2010-07-01
Platinum-catalyzed intramolecular hydroarylation of allenyl arenes: efficient synthesis of 1,4-dihydronaphthalenes.
2010-06-04
Ethoxycarbonyl-based organic electrode for Li-batteries.
2010-05-12
Reactions of the terminal Ni(II)-OH group in substitution and electrophilic reactions with carbon dioxide and other substrates: structural definition of binding modes in an intramolecular Ni(II)...Fe(II) bridged site.
2010-04-07
Efficacy of vaporised ethyl formate/carbon dioxide formulation against stored-grain insects: effect of fumigant concentration, exposure time and two grain temperatures.
2010-04
Field evaluation of vaporised ethyl formate and carbon dioxide for fumigation of stored wheat.
2010-04
Another paradigm in solvent extraction-based microencapsulation technologies.
2010-03-08
Solvent-free, microwave assisted synthesis of polyhalo heterocyclic ketene aminals as novel anti-cancer agents.
2010-01-01
Identification of ethyl formate as a quality marker of the fermented off-note in coffee by a nontargeted chemometric approach.
2009-11-11
Modelling the kinetics of ethyl formate sorption by wheat using batch experiments.
2009-09
Tumor-specific cytotoxic activity of 1,2,3,4-tetrahydroisoquinoline derivatives against human oral squamous cell carcinoma cell lines.
2009-08
Synthesis and antitubercular screening of imidazole derivatives.
2009-08
Inhibition of human sirtuins by in situ generation of an acetylated lysine-ADP-ribose conjugate.
2009-05-27
Primary Structure Revision and Active Site Mapping of E. Coli Isoleucyl-tRNA Synthetase by Means of Maldi Mass Spectrometry.
2009-03-06
Toxicities of 31 volatile low molecular weight compounds against Aedes aegypti and Culex quinquefasciatus.
2009-03
Modeling the heat and mass transfers in temperature-swing adsorption of volatile organic compounds onto activated carbons.
2009-02-15
Synthesis and antiprotozoal activity of novel 1-methylbenzimidazole derivatives.
2009-02-15
Mutagenesis identifies the critical amino acid residues of human endonuclease G involved in catalysis, magnesium coordination, and substrate specificity.
2009-01-15
Computing highly correlated positions using mutual information and graph theory for G protein-coupled receptors.
2009
Antithyroid drug carbimazole and its analogues: synthesis and inhibition of peroxidase-catalyzed iodination of L-tyrosine.
2008-11-27
Ethyl 3,5-dimethyl-1H-pyrrole-2-carboxyl-ate.
2008-09-24
Leishmania donovani pteridine reductase 1: biochemical properties and structure-modeling studies.
2008-09
Biological activity of amide derivatives of lysine.
2008-07-24
Gas-phase fragmentation study of novel synthetic 1,5-benzodiazepine derivatives using electrospray ionization tandem mass spectrometry.
2008-07
Reactions of the (2-pyridyl) pyrrolide platinum(II) complex driven by sterically encumbered chelation: a model for the reversible attack of alcohol at the coordinated carbon monoxide.
2008-06-16
Synthesis of (+)-cortistatin A.
2008-06-11
Synthesis of 5-(thiazol-5-yl)-4,5-dihydroisoxazoles from 3-chloropentane-2,4-dione.
2008-05-29
Synthesis, structure elucidation and identification of antitumoural properties of novel fused 1,2,4-triazine aryl derivatives.
2008-05
Fumigation of wheat using liquid ethyl formate plus methyl isothiocyanate in 50-tonne farm bins.
2008-04
Photoluminescence and electroluminescence of methoxy and carboethoxy derivatives of 1,3-diphenyl-1H-pyrazolo[3,4-b]quinoline.
2008-01
Efficient construction of tri- and tetracyclic heterocycles from linear 1,6-dienes by a domino reaction.
2008
Diethyl 5,5'-thio-bis[2-amino-4-(4-fluoro-phen-yl)-1-phenyl-1H-pyrrole-3-carboxyl-ate].
2007-12-06
PYRROLO[1,2-b][1,2,5]BENZOTHIADIAZEPINES (PBTDs) induce apoptosis in K562 cells.
2007-11-09
Simultaneous screening analysis of multiple beta-blockers in urine by gas chromatography-mass spectrometry in selected ion monitoring mode.
2007-10-10
Rate constants of hydroperoxyl radical addition to cyclic nitrones: a DFT study.
2007-10-04
Synthesis, Ti(IV) intake by apotransferrin and cytotoxic properties of functionalized titanocene dichlorides.
2007-09
The atmospheric oxidation of diethyl ether: chemistry of the C2H5-O-CH(O.)CH3 radical between 218 and 335 K.
2007-08-21
Ethyl formate as a postharvest fumigant for selected pests of table grapes.
2007-08
Optical absorption of methoxy and carboethoxy derivatives of 1,3-diphenyl-1H-pyrazolo[3,4-b]quinoline.
2007-07
Synthesis of pyrrolo[2,3-d]pyridazinones as potent, subtype selective PDE4 inhibitors.
2007-06
Isomer-specific fuel destruction pathways in rich flames of methyl acetate and ethyl formate and consequences for the combustion chemistry of esters.
2007-05-17
The proton inventory technique in a dual mechanistic system: the spontaneous hydrolysis of ethyl formate.
2007-03
Reverse micelle-based microencapsulation of oxytetracycline hydrochloride into poly-d,l-lactide-co-glycolide microspheres.
2007-02
Evaluation of microwave irradiation for analysis of carbonyl sulfide, carbon disulfide, cyanogen, ethyl formate, methyl bromide, sulfuryl fluoride, propylene oxide, and phosphine in hay.
2007-01-10
Synthesis of modified nucleosides for incorporation of formyletheno and carboxyetheno adducts of adenine nucleosides into oligonucleotides.
2007
Photosensitizers containing the 1,8-naphthyridyl moiety and their use in dye-sensitized solar cells.
2006-12-11
An efficient synthesis of tetramic acid derivatives with extended conjugation from L-ascorbic acid.
2006-12-06
One-shot double elimination process: a practical and concise protocol for diaryl acetylenes.
2006-09-18
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:36:01 GMT 2025
Edited
by admin
on Mon Mar 31 18:36:01 GMT 2025
Record UNII
0K3E2L5553
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Ethyl formate
FCC   FHFI   HSDB   MI   USP-RS  
Systematic Name English
FEMA NO. 2434
Preferred Name English
Ethyl formate [MI]
Common Name English
Ethyl formic ester
Common Name English
Formic acid, ethyl ester
Common Name English
Ethyl formate [FHFI]
Common Name English
Ethyl formate [HSDB]
Common Name English
Ethyl formate [USP-RS]
Common Name English
Formic ether
Common Name English
Ethyl methanoate
Systematic Name English
NSC-406578
Code English
Ethyl formate [FCC]
Common Name English
Classification Tree Code System Code
CFR 21 CFR 184.1295
Created by admin on Mon Mar 31 18:36:01 GMT 2025 , Edited by admin on Mon Mar 31 18:36:01 GMT 2025
EPA PESTICIDE CODE 43102
Created by admin on Mon Mar 31 18:36:01 GMT 2025 , Edited by admin on Mon Mar 31 18:36:01 GMT 2025
JECFA EVALUATION ETHYL FORMATE
Created by admin on Mon Mar 31 18:36:01 GMT 2025 , Edited by admin on Mon Mar 31 18:36:01 GMT 2025
Code System Code Type Description
CAS
109-94-4
Created by admin on Mon Mar 31 18:36:01 GMT 2025 , Edited by admin on Mon Mar 31 18:36:01 GMT 2025
PRIMARY
EVMPD
SUB174836
Created by admin on Mon Mar 31 18:36:01 GMT 2025 , Edited by admin on Mon Mar 31 18:36:01 GMT 2025
PRIMARY
WIKIPEDIA
ETHYL FORMATE
Created by admin on Mon Mar 31 18:36:01 GMT 2025 , Edited by admin on Mon Mar 31 18:36:01 GMT 2025
PRIMARY
RS_ITEM_NUM
1265606
Created by admin on Mon Mar 31 18:36:01 GMT 2025 , Edited by admin on Mon Mar 31 18:36:01 GMT 2025
PRIMARY
MERCK INDEX
m5132
Created by admin on Mon Mar 31 18:36:01 GMT 2025 , Edited by admin on Mon Mar 31 18:36:01 GMT 2025
PRIMARY Merck Index
ALANWOOD
ethyl formate
Created by admin on Mon Mar 31 18:36:01 GMT 2025 , Edited by admin on Mon Mar 31 18:36:01 GMT 2025
PRIMARY
NSC
406578
Created by admin on Mon Mar 31 18:36:01 GMT 2025 , Edited by admin on Mon Mar 31 18:36:01 GMT 2025
PRIMARY
HSDB
943
Created by admin on Mon Mar 31 18:36:01 GMT 2025 , Edited by admin on Mon Mar 31 18:36:01 GMT 2025
PRIMARY
EVMPD
SUB115726
Created by admin on Mon Mar 31 18:36:01 GMT 2025 , Edited by admin on Mon Mar 31 18:36:01 GMT 2025
PRIMARY
PUBCHEM
8025
Created by admin on Mon Mar 31 18:36:01 GMT 2025 , Edited by admin on Mon Mar 31 18:36:01 GMT 2025
PRIMARY
FDA UNII
0K3E2L5553
Created by admin on Mon Mar 31 18:36:01 GMT 2025 , Edited by admin on Mon Mar 31 18:36:01 GMT 2025
PRIMARY
SMS_ID
100000161167
Created by admin on Mon Mar 31 18:36:01 GMT 2025 , Edited by admin on Mon Mar 31 18:36:01 GMT 2025
PRIMARY
EPA CompTox
DTXSID6040117
Created by admin on Mon Mar 31 18:36:01 GMT 2025 , Edited by admin on Mon Mar 31 18:36:01 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-721-0
Created by admin on Mon Mar 31 18:36:01 GMT 2025 , Edited by admin on Mon Mar 31 18:36:01 GMT 2025
PRIMARY
MESH
C510888
Created by admin on Mon Mar 31 18:36:01 GMT 2025 , Edited by admin on Mon Mar 31 18:36:01 GMT 2025
PRIMARY
CHEBI
52342
Created by admin on Mon Mar 31 18:36:01 GMT 2025 , Edited by admin on Mon Mar 31 18:36:01 GMT 2025
PRIMARY
JECFA MONOGRAPH
311
Created by admin on Mon Mar 31 18:36:01 GMT 2025 , Edited by admin on Mon Mar 31 18:36:01 GMT 2025
PRIMARY