2-ACETYLPYRROLE

Details

Stereochemistry	ACHIRAL
Molecular Formula	C6H7NO
Molecular Weight	109.1259
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CC(=O)C1=CC=CN1

InChI

InChIKey=IGJQUJNPMOYEJY-UHFFFAOYSA-N

InChI=1S/C6H7NO/c1-5(8)6-3-2-4-7-6/h2-4,7H,1H3

HIDE SMILES / InChI

Molecular Formula	C6H7NO
Molecular Weight	109.1259
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
Identification of hydroxycinnamic acid-maillard reaction products in low-moisture baking model systems.	2009-11-11	19817410
Role of roasting conditions in the profile of volatile flavor chemicals formed from coffee beans.	2009-07-08	19579294
2- and 3-acetylpyrroles: a combined calorimetric and computational study.	2009-04-16	19320446
3-(4-Methoxy-phen-yl)-1-(2-pyrrol-yl)prop-2-en-1-one.	2008-09-13	21201128
3-[4-(Dimethyl-amino)phen-yl]-1-(2-pyrrol-yl)prop-2-en-1-one.	2008-05-21	21202634
(2E)-3-(4-Chloro-phen-yl)-1-(1H-pyrrol-2-yl)prop-2-en-1-one.	2008-04-18	21202354
Chlorido{2-[1-(2-pyridylmethyl-imino)eth-yl]pyrrolato-κN,N',N''}copper(II).	2008-03-14	21202015
Bis(ketopyrrolyl) complexes of Co(II) stabilised by trimethylphosphine ligands.	2007-12-14	18026596
Influence of epicatechin reactions on the mechanisms of Maillard product formation in low moisture model systems.	2007-01-24	17227073
Synthesis, spectroscopic, and antimicrobial studies on bivalent nickel and copper complexes of bis(thiosemicrbazone).	2007	18273385
Characterisation of glycoprotein ligands synthesised using solid-phase combinatorial chemistry.	2005-05-20	15974122
Aroma compounds in sweet whey powder.	2004-12	15545366
Synthesis of novel dihydropyridine, dihydropyrimidine, dithioacetal and chalcone derivatives from formylchromones.	2004-03	15191212
Effect of the pyrrole polymerization mechanism on the antioxidative activity of nonenzymatic browning reactions.	2003-09-10	12952422
Pyrrole alkaloids from Bolbostemma paniculatum.	2003-09	12931847
Thermal decomposition of specifically phosphorylated D-glucoses and their role in the control of the Maillard reaction.	2003-05-21	12744667
1-(2-Pyridyl) ethan-1-one 8-quinolylhydrazone and 1-(1H-pyrrol-2-yl) ethan-1-one 8-quinolylhydrazone.	2002-11	12415168
Antioxidative activity of heterocyclic compounds found in coffee volatiles produced by Maillard reaction.	2002-09-11	12207495
Selective cleavage of P-N bonds and the conversion of rhodium N-pyrrolyl phosphine complexes into diphosphoxane-bridged dimers.	2002-04-08	11925157
Aging of proteins: immunological detection of a glucose-derived pyrrole formed during maillard reaction in vivo.	1989-03-05	2917974

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:49:11 GMT 2025` Edited by `admin` on `Mon Mar 31 18:49:11 GMT 2025`
Record UNII	9K28W7PM6N
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

METHYL 2-PYRROLYL KETONE

Preferred Name

English

2-ACETYLPYRROLE

Systematic Name

English

2-ACETYLPYRROLE [FCC]

Common Name

English

1-(2-PYRROLYL)-1-ETHANONE

Systematic Name

English

FEMA NO. 3202

Code

English

ETHANONE, 1-(1H-PYRROL-2-YL)-

Systematic Name

English

2-PYRROLYLETHANONE

Systematic Name

English

KETONE, METHYL PYRROL-2-YL

Systematic Name

English

1-(1H-PYRROL-2-YL)ETHANONE

Systematic Name

English

2-PYRROLYL METHYL KETONE

Systematic Name

English

NSC-42861

Code

English

1-(1H-PYRROL-2-YL)ETHAN-1-ONE

Systematic Name

English

METHYL 2-PYRROLYL KETONE [FHFI]

Common Name

English

METHYL PYRROL-2-YL KETONE

Systematic Name

English

Classification Tree Code System Code

JECFA EVALUATION

METHYL 2-PYRROLYL KETONE