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

Details

Stereochemistry ACHIRAL
Molecular Formula C8H6O2
Molecular Weight 134.132
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TEREPHTHALDEHYDE

SMILES

O=CC1=CC=C(C=O)C=C1

InChI

InChIKey=KUCOHFSKRZZVRO-UHFFFAOYSA-N
InChI=1S/C8H6O2/c9-5-7-1-2-8(6-10)4-3-7/h1-6H

HIDE SMILES / InChI

Molecular Formula C8H6O2
Molecular Weight 134.132
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Exceptional thermal stability in a supramolecular organic framework: porosity and gas storage.
2010-10-20
Stereoselective synthesis of ring C-hexasubstituted trianglamines.
2010-09-07
The effect of tribendimidine and its metabolites against Necator americanus in golden hamsters and Nippostrongylus braziliensis in rats.
2010-03
Synthesis and Characterization of New Optically Active Poly (ethyl L-lysinamide)s and Poly (ethyl L-lysinimide)s.
2010
Metabolism and disposition of tribendimidine and its metabolites in healthy Chinese volunteers.
2010
(E)-1-(4-Nitro-phen-yl)-2-(4-{[(E)-2-(4-nitro-phen-yl)hydrazinyl-idene]meth-yl}benzyl-idene)hydrazine dihydrate.
2009-12-19
The in vitro and in vivo effect of tribendimidine and its metabolites against Clonorchis sinensis.
2009-11
1,4-Bis(2-pyridylimino-meth-yl)benzene.
2009-10-07
Synthesis, spectral characterization, catalytic and antibacterial studies of new Ru(III) Schiff base complexes containing chloride/bromide and triphenylphosphine/arsine as co-ligands.
2009-10-01
3,6,9,16,19,22-Hexaazatricyclo-[22.2.2.2]triaconta-1(27),11 (30),-12,14(29),24(28),25-hexaene hexakis(p-toluenesulfonate) dihydrate.
2009-09-09
1,4-Bis{(+)-(S)-[1-(1-naphth-yl)eth-yl]imino-meth-yl}benzene.
2009-09-05
Transformations of N-confused porphyrin triggered by insertion of silicon(IV).
2009-08-03
Degradation of carbofuran-contaminated water by the Fenton process.
2009-07-15
(2E,2'E)-1,1'-Bis(2,5-dimethyl-3-thien-yl)-3,3'-(p-phenyl-ene)diprop-2-en-1-one.
2009-07-01
A novel class of extended pi-conjugated systems: one-pot synthesis of bis-3-aminoimidazo[1,2-a]pyridines, pyrimidines and pyrazines.
2009-05
A crystalline imine-linked 3-D porous covalent organic framework.
2009-04-08
1,4-Bis(benzimidazol-2-yl)benzene dimethyl-formamide disolvate.
2009-02-13
Synthesis and characterization of biologically significant 5,5'-(1,4-phenylene)bis(1-N-alkoxyphthalimido-3-aryl-2-pyrazoline) derivatives.
2008-12
Novel dimeric cholesteryl-based A(LS)2 low-molecular-mass gelators with a benzene ring in the linker.
2008-11-01
A polymorph of terephthalaldehyde.
2008-07-23
N-{(E)-4-[(E)-(Dodecyl-imino)meth-yl]benzyl-idene}dodecan-1-imine.
2008-02-06
Equilibrium constants in reactions of 2-aminoethanol and ammonia with isophthalaldehyde and terephthalaldehyde.
2007-12-20
Dimethyl 4-(4-formyl-phen-yl)-2,6-di-methyl-1,4-dihydro-pyridine-3,5-dicar-boxyl-ate.
2007-12-18
Dichlorido(3,5-dimethyl-1H-pyrazole)[(3,5-dimethyl-1H-pyrazol-1-yl)(o-tol-yl)methanone]palladium(II).
2007-12-18
Synthesis of novel derivatives of 4-amino-3-(2-furyl)-5-mercapto-1,2,4-triazole as potential HIV-1 NNRTIs.
2007-08-22
Matrix-isolation infrared spectroscopy of the rotational isomers of 1,2-, 1,3-, and 1,4-benzenedicarboxaldehyde.
2007-08-02
Similarities and differences between azomethines and ketimines: synthesis, materials characterization and structure of novel imines compounds.
2007-04
Microcapsules of PEGylated gold nanoparticles prepared by fluid-fluid interfacial assembly.
2007-02
Copper(II) complexes with ligands derived from 4-amino-2,3-dimethyl-1-phenyl-3-pyrazolin-5-one: synthesis and biological activity.
2006-11-17
Identification of potent, selective protein kinase C inhibitors based on a phorbol skeleton.
2006-09-18
Covalent microcontact printing of proteins for cell patterning.
2006-08-16
Shaken not stirred: a facile synthesis of 1,4-bis(furo[2,3-d]-pyrimidine-2,4(1H,3H)-dione-5-yl)benzenes by one-pot reaction of isocyanides, N,N'-dimethylbarbituric acid, and terephthaldialdehyde.
2006-07-15
Unprecedented selectivity in the formation of large-ring oligoimines from conformationally bistable chiral diamines.
2006-07-06
Determination of orthophthalaldehyde in air using 2,4-dinitrophenylhydrazine-impregnated silica cartridge and high-performance liquid chromatography.
2006-05-26
Trianglamines--readily prepared, conformationally flexible inclusion-forming chiral hexamines.
2006-02-08
Strong covalent hydration of terephthalaldehyde.
2005-11-24
Reversible covalent patterning of self-assembled monolayers on gold and silicon oxide surfaces.
2005-07-05
Electrospray mass spectrometry studies of macromolecules containing 1,3-oxazolidine moieties.
2004
Electrospray mass spectrometry determination of poly(oxazolidine acetal).
2003
Application of Ugi reactions in synthesis of divalent neoglycoconjugates: evidence that the sugars are presented in restricted conformation.
2001-08-23
Synthesis and characterization of coronanes: multicyclopropane-fused macrocyclic arrays.
2001-04-06
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:56:37 GMT 2025
Edited
by admin
on Mon Mar 31 19:56:37 GMT 2025
Record UNII
M2Y6E4N2TS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-13395
Preferred Name English
TEREPHTHALDEHYDE
Common Name English
1,4-TEREPHTHALDICARBALDEHYDE
Common Name English
4-FORMYLBENZALDEHYDE
Systematic Name English
1,4-BENZENEDICARBOXALDEHYDE
Systematic Name English
1,4-BENZENEDICARBALDEHYDE
Systematic Name English
P-BENZENEDICARBOXALDEHYDE
Common Name English
P-BENZENEDIALDEHYDE
Common Name English
TEREPHTHALIC ALDEHYDE
Common Name English
1,4-BENZENEDIALDEHYDE
Systematic Name English
1,4-DIFORMYLBENZENE
Systematic Name English
P-DIFORMYLBENZENE
Common Name English
P-PHTHALDIALDEHYDE
Common Name English
TEREPHTHALDIALDEHYDE
Common Name English
P-FORMYLBENZALDEHYDE
Common Name English
Code System Code Type Description
CAS
623-27-8
Created by admin on Mon Mar 31 19:56:37 GMT 2025 , Edited by admin on Mon Mar 31 19:56:37 GMT 2025
PRIMARY
PUBCHEM
12173
Created by admin on Mon Mar 31 19:56:37 GMT 2025 , Edited by admin on Mon Mar 31 19:56:37 GMT 2025
PRIMARY
NSC
13395
Created by admin on Mon Mar 31 19:56:37 GMT 2025 , Edited by admin on Mon Mar 31 19:56:37 GMT 2025
PRIMARY
ECHA (EC/EINECS)
210-784-8
Created by admin on Mon Mar 31 19:56:37 GMT 2025 , Edited by admin on Mon Mar 31 19:56:37 GMT 2025
PRIMARY
FDA UNII
M2Y6E4N2TS
Created by admin on Mon Mar 31 19:56:37 GMT 2025 , Edited by admin on Mon Mar 31 19:56:37 GMT 2025
PRIMARY
EPA CompTox
DTXSID6060769
Created by admin on Mon Mar 31 19:56:37 GMT 2025 , Edited by admin on Mon Mar 31 19:56:37 GMT 2025
PRIMARY