3-Hydroxybenzaldehyde

Details

Stereochemistry	ACHIRAL
Molecular Formula	C7H6O2
Molecular Weight	122.1213
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

OC1=CC=CC(C=O)=C1

InChI

InChIKey=IAVREABSGIHHMO-UHFFFAOYSA-N

InChI=1S/C7H6O2/c8-5-6-2-1-3-7(9)4-6/h1-5,9H

HIDE SMILES / InChI

Molecular Formula	C7H6O2
Molecular Weight	122.1213
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
Aromatic aldehyde dehydrogenase from Pseudomonas putida N.C.I.B. 9869.	1975	236959
The aromatic alcohol dehydrogenases in Pseudomonas putida N.C.I.B. 9869 grown on 3,5-xylenol and p-cresol.	1978 Nov 1	743216
GC/ITMS measurement of carbonyls and multifunctional carbonyls in PM2.5 particles emitted from motor vehicles.	2001 May-Jun	11417634
Effects of aldehyde dehydrogenase-2 genetic polymorphisms on metabolism of structurally different aldehydes in human liver.	2002 Jan	11744614
IR spectral and structural changes caused by the conversion of 3-hydroxybenzaldehyde into the oxyanion.	2003 May	12714077
Subphthalocyanines: tuneable molecular scaffolds for intramolecular electron and energy transfer processes.	2004 May 26	15149228
Synthesis and characterization of a novel functionalized azanonaborane cluster for boron neutron capture therapy.	2005 Jun 7	15917896
A new copper(I)-tetrahydrosalen-catalyzed asymmetric Henry reaction and its extension to the synthesis of (S)-norphenylephrine.	2007	17068834
2'-(3-Hydroxy-benzyl-idene)pyrazine-2-carbohydrazide monohydrate.	2007 Dec 6	21200959
Redetermination of 4-hydroxy-benzaldehyde.	2007 Dec 6	21200751
Combinatorial synthesis and characterization of new asymmetric porphyrins as potential photosensitizers in photodynamic therapy.	2007 Jul	17896942
Low-energy collision-induced fragmentation of negative ions derived from ortho-, meta-, and para-hydroxyphenyl carbaldehydes, ketones, and related compounds.	2007 Sep	17694503
Cationic porphyrin induced a telomeric DNA to g-quadruplex form in water.	2008	18350116
Asymmetric total synthesis of (-)-quinocarcin.	2008 Jun 4	18454525
1,2-Bis(3-hydroxy-benzyl-idene)diazane.	2009 Jul 18	21583612
3-[1-(3-Hydroxy-benz-yl)-1H-benz-imid-azol-2-yl]phenol.	2009 May 23	21583223
Ethyl 4-(3-hydroxy-phen-yl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexa-hydro-quinoline-3-carboxyl-ate.	2009 Oct 7	21578275
(E)-N'-(3-Hy-droxy-benzyl-idene)-3-nitro-benzohydrazide.	2010 Dec 4	21522781
Dimethyl 4-(3-hydroxy-phen-yl)-2,6-dimethyl-1,4-dihydro-pyridine-3,5-dicarboxyl-ate.	2010 Mar 31	21580781
(E)-1-[4-(Hex-yloxy)phen-yl]-3-(3-hy-droxy-phen-yl)prop-2-en-1-one.	2010 Nov 24	21589557
N'-(3-Hy-droxy-benzyl-idene)-4-nitro-benzohydrazide.	2010 Oct 31	21589165

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 18:38:26 GMT 2023` Edited by `admin` on `Fri Dec 15 18:38:26 GMT 2023`
Record UNII	8Z2819J40E
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

3-Hydroxybenzaldehyde

Systematic Name

English

Hydroxybenzaldehyde, 3-

Common Name

English

m-Formylphenol

Systematic Name

English

Benzaldehyde, 3-hydroxy-

Systematic Name

English

m-Hydroxybenzaldehyde

Systematic Name

English

3-Formylphenol

Systematic Name

English

NSC-3504

Code

English

Benzaldehyde, m-hydroxy-

Systematic Name

English

Code System Code Type Description

NSC

3504