U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C8H6O3
Molecular Weight 150.1314
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PIPERONAL

SMILES

O=CC1=CC2=C(OCO2)C=C1

InChI

InChIKey=SATCULPHIDQDRE-UHFFFAOYSA-N
InChI=1S/C8H6O3/c9-4-6-1-2-7-8(3-6)11-5-10-7/h1-4H,5H2

HIDE SMILES / InChI

Molecular Formula C8H6O3
Molecular Weight 150.1314
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
[Morphological features of the thymus in heliotrin hepatitis upon administration of immunostimulators].
2001
Antioxidant properties of 8.0.4'-neolignans.
2001 Nov
A short synthesis of (+/-)-epiasarinin.
2002 Apr 4
[Comparative evaluation of antioxidant properties of neoselen and berberin in chronic heliotrinal hepatitis].
2002 Apr-Jun
[Succivil efficacy in endogenous intoxication].
2003 Jul-Aug
Chemical profiling of 3,4-methylenedioxymethamphetamine (MDMA) tablets seized in Hong Kong.
2003 Nov
First total synthesis of justicidone, a p-quinone-lignan derivative from Justicia hyssopifolia.
2005 Aug
A study of impurities in intermediates and 3,4-methylenedioxymethamphetamine (MDMA) samples produced via reductive amination routes.
2005 Dec 20
Determination of synthesis method of ecstasy based on the basic impurities.
2005 Sep 10
Synthesis, Spectral, and Biological Properties of Copper(II) Complexes of Thiosemicarbazones of Schiff Bases Derived from 4-Aminoantipyrine and Aromatic Aldehydes.
2006
Synthesis of 7-deoxypancratistatin from carbohydrates by the use of olefin metathesis.
2006 Apr 12
The fumigant and repellent activity of aliphatic lactones against Pediculus humanus capitis (Anoplura: Pediculidae).
2006 Feb
Highly efficient cyclization of o-iodobenzoates with aldehydes catalyzed by cobalt bidentate phosphine complexes: a novel entry to chiral phthalides.
2007
Development and validation of an RP-HPLC method for quantitative determination of vanillin and related phenolic compounds in Vanilla planifolia.
2007 Jan
Alpha-phenyl-N-tert-butyl nitrone (PBN) derivatives: synthesis and protective action against microvascular damages induced by ischemia/reperfusion.
2007 May 15
Influence of chalcone analogues on serum glucose levels in hyperglycemic rats.
2008 Feb 15
Synthesis and use of 4-peptidylhydrazido-N-hexyl-1,8-naphthalimides as fluorogenic histochemical substrates for dipeptidyl peptidase IV and tripeptidyl peptidase I.
2009 Jan
A combined experimental and theoretical study of the polar [3 + 2] cycloaddition of electrophilically activated carbonyl ylides with aldehydes and imines.
2009 Mar 6
Total synthesis of (+)-virgatusin via AlCl3-catalyzed [3+2] cycloaddition.
2009 Sep 14
(E)-N'-(1,3-Benzodioxol-5-ylmethyl-ene)nicotinohydrazide monohydrate.
2009 Sep 5
Preparation and In vitro / In vivo characterization of spray dried microsphere formulation encapsulating 4-chlorocurcumin.
2010 May
N-[(E)-1,3-Benzodioxol-5-yl-methyl-idene]-4-methyl-aniline.
2010 Nov 24
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:08:54 GMT 2023
Edited
by admin
on Fri Dec 15 16:08:54 GMT 2023
Record UNII
KE109YAK00
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PIPERONAL
FCC   FHFI   HSDB   MART.   MI   WHO-DD  
Common Name English
PIPERONAL (CONSTITUENT OF BLACK PEPPER) [DSC]
Common Name English
HELIOTROPINE [INCI]
Common Name English
PIPERONAL [HSDB]
Common Name English
DIOXYMETHYLENEPROTOCATECHUIC ALDEHYDE
Common Name English
3,4-(METHYLENEDIOXY)BENZALDEHYDE
Systematic Name English
2H-BENZO(3,4-D)-1,3-DIOXOLAN-5-YLFORMALDEHYDE
Systematic Name English
NSC-26826
Code English
PIPERONAL [FHFI]
Common Name English
1,3-BENZODIOXOLE-6-CARBOXALDEHYDE
Systematic Name English
PIPERONAL [FCC]
Common Name English
FEMA NO. 2911
Code English
GELIOTROPIN
Common Name English
Piperonal [WHO-DD]
Common Name English
HELIOTROPINE
INCI  
INCI  
Official Name English
PIPERONAL [MI]
Common Name English
PIPERONAL [MART.]
Common Name English
PIPERONYLALDEHYDE
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION PIPERONAL
Created by admin on Fri Dec 15 16:08:55 GMT 2023 , Edited by admin on Fri Dec 15 16:08:55 GMT 2023
DEA NO. 8750
Created by admin on Fri Dec 15 16:08:55 GMT 2023 , Edited by admin on Fri Dec 15 16:08:55 GMT 2023
Code System Code Type Description
EVMPD
SUB37596
Created by admin on Fri Dec 15 16:08:55 GMT 2023 , Edited by admin on Fri Dec 15 16:08:55 GMT 2023
PRIMARY
WIKIPEDIA
PIPERONAL
Created by admin on Fri Dec 15 16:08:55 GMT 2023 , Edited by admin on Fri Dec 15 16:08:55 GMT 2023
PRIMARY
HSDB
581
Created by admin on Fri Dec 15 16:08:55 GMT 2023 , Edited by admin on Fri Dec 15 16:08:55 GMT 2023
PRIMARY
EPA CompTox
DTXSID7025924
Created by admin on Fri Dec 15 16:08:55 GMT 2023 , Edited by admin on Fri Dec 15 16:08:55 GMT 2023
PRIMARY
RXCUI
33753
Created by admin on Fri Dec 15 16:08:55 GMT 2023 , Edited by admin on Fri Dec 15 16:08:55 GMT 2023
PRIMARY RxNorm
SMS_ID
100000129172
Created by admin on Fri Dec 15 16:08:55 GMT 2023 , Edited by admin on Fri Dec 15 16:08:55 GMT 2023
PRIMARY
CHEBI
8240
Created by admin on Fri Dec 15 16:08:55 GMT 2023 , Edited by admin on Fri Dec 15 16:08:55 GMT 2023
PRIMARY
NSC
26826
Created by admin on Fri Dec 15 16:08:55 GMT 2023 , Edited by admin on Fri Dec 15 16:08:55 GMT 2023
PRIMARY
FDA UNII
KE109YAK00
Created by admin on Fri Dec 15 16:08:55 GMT 2023 , Edited by admin on Fri Dec 15 16:08:55 GMT 2023
PRIMARY
JECFA MONOGRAPH
808
Created by admin on Fri Dec 15 16:08:55 GMT 2023 , Edited by admin on Fri Dec 15 16:08:55 GMT 2023
PRIMARY
DAILYMED
KE109YAK00
Created by admin on Fri Dec 15 16:08:55 GMT 2023 , Edited by admin on Fri Dec 15 16:08:55 GMT 2023
PRIMARY
MESH
C005454
Created by admin on Fri Dec 15 16:08:55 GMT 2023 , Edited by admin on Fri Dec 15 16:08:55 GMT 2023
PRIMARY
PUBCHEM
8438
Created by admin on Fri Dec 15 16:08:55 GMT 2023 , Edited by admin on Fri Dec 15 16:08:55 GMT 2023
PRIMARY
MERCK INDEX
m8858
Created by admin on Fri Dec 15 16:08:55 GMT 2023 , Edited by admin on Fri Dec 15 16:08:55 GMT 2023
PRIMARY Merck Index
CAS
120-57-0
Created by admin on Fri Dec 15 16:08:55 GMT 2023 , Edited by admin on Fri Dec 15 16:08:55 GMT 2023
PRIMARY
ECHA (EC/EINECS)
204-409-7
Created by admin on Fri Dec 15 16:08:55 GMT 2023 , Edited by admin on Fri Dec 15 16:08:55 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
USP-DSC
PARENT->PRECURSOR
PARENT->PRECURSOR
Related Record Type Details
PARENT -> IMPURITY