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
Aging of proteins: immunological detection of a glucose-derived pyrrole formed during maillard reaction in vivo.	1989 Mar 5	2917974
Selective cleavage of P-N bonds and the conversion of rhodium N-pyrrolyl phosphine complexes into diphosphoxane-bridged dimers.	2002 Apr 8	11925157
1-(2-Pyridyl) ethan-1-one 8-quinolylhydrazone and 1-(1H-pyrrol-2-yl) ethan-1-one 8-quinolylhydrazone.	2002 Nov	12415168
Antioxidative activity of heterocyclic compounds found in coffee volatiles produced by Maillard reaction.	2002 Sep 11	12207495
Thermal decomposition of specifically phosphorylated D-glucoses and their role in the control of the Maillard reaction.	2003 May 21	12744667
Pyrrole alkaloids from Bolbostemma paniculatum.	2003 Sep	12931847
Effect of the pyrrole polymerization mechanism on the antioxidative activity of nonenzymatic browning reactions.	2003 Sep 10	12952422
Aroma compounds in sweet whey powder.	2004 Dec	15545366
Synthesis of novel dihydropyridine, dihydropyrimidine, dithioacetal and chalcone derivatives from formylchromones.	2004 Mar	15191212
Characterisation of glycoprotein ligands synthesised using solid-phase combinatorial chemistry.	2005 May 20	15974122
Influence of epicatechin reactions on the mechanisms of Maillard product formation in low moisture model systems.	2007 Jan 24	17227073
(2E)-3-(4-Chloro-phen-yl)-1-(1H-pyrrol-2-yl)prop-2-en-1-one.	2008 Apr 18	21202354
Chlorido{2-[1-(2-pyridylmethyl-imino)eth-yl]pyrrolato-κN,N',N''}copper(II).	2008 Mar 14	21202015
3-[4-(Dimethyl-amino)phen-yl]-1-(2-pyrrol-yl)prop-2-en-1-one.	2008 May 21	21202634
3-(4-Methoxy-phen-yl)-1-(2-pyrrol-yl)prop-2-en-1-one.	2008 Sep 13	21201128
Role of roasting conditions in the profile of volatile flavor chemicals formed from coffee beans.	2009 Jul 8	19579294
Identification of hydroxycinnamic acid-maillard reaction products in low-moisture baking model systems.	2009 Nov 11	19817410

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 17:36:06 GMT 2023` Edited by `admin` on `Fri Dec 15 17:36:06 GMT 2023`
Record UNII	9K28W7PM6N
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

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

METHYL 2-PYRROLYL KETONE

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