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2,3-Dihydroxybenzaldehyde - 97%, high purity , CAS No.24677-78-9

1 Citations

COA

Grade & Purity:

≥97%

Cas Number: 24677-78-9
Molecular Weight: 138.12
Beilstein Registry Number: 2041781
EC Number: 246-398-1
MDL number: MFCD00003324
PubChem CID: 90579
PubChem SID: 504756037

In stock

Item Number

D122910

Grouped product items
SKU	Size	Availability	Price
D122910-1g	1g	3	$11.90
D122910-5g	5g	3	$45.90
D122910-10g	10g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$81.90
D122910-25g	25g	3	$155.90
D122910-100g	100g	2	$519.90

View related series

aldehyde (388) Carbonyl compound (2335)

Basic Description

Synonyms	h-pro-ome hcl \| BCP25752 \| NSC146456 \| NSC-146456 \| o-Pyrocatechualdehyde \| A817431 \| DIHYDROXYBENZALDEHYDE, 2,3- \| 2,3-dihydroxy benzaldehyde \| EINECS 246-398-1 \| BDBM111044 \| SCHEMBL36440 \| 3-hydroxysalicylaldehyde \| 5,6-Dihydroxybenzaldehyde \| Methanam
Specifications & Purity	≥97%
Storage Temp	Store at 2-8°C,Argon charged
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	An antifungal and antimicrobial agent. In one study, 2,3-dihydroxybenzaldehyde was identified as a potent chemosensitizing agent that targets the cell wall. Furthermore, an additional study confirmed that 2,3-dihydroxybenzaldehyde disrupted the MAPK pathway via the SOD2 gene. The same study also found that when used with other antifungal agents such as fludioxonil, it prevented fungal mutants from developing tolerance to fludioxonil. Also found to be useful in synthesis of Amberlite XAD resins that can be used to preconcentrate metals from soil samples. 2,3-Dihydroxybenzaldehyde has been used to synthesize the copper(II) complex of Schiff base. It is also used to synthesize 2-ethoxy-3-hydroxy-4-nitrobenzoic acid

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic oxygen compounds
  - Class Organooxygen compounds
    - Subclass Carbonyl compounds
      - Level5 Aldehydes
        Level6 Aryl-aldehydes
        Level7 Benzaldehydes
        Level8 Hydroxybenzaldehydes

Kingdom	Organic compounds
Superclass	Organic oxygen compounds
Class	Organooxygen compounds
Subclass	Carbonyl compounds
Intermediate Tree Nodes	Aldehydes - Aryl-aldehydes - Benzaldehydes
Direct Parent	Hydroxybenzaldehydes
Alternative Parents	Catechols Benzoyl derivatives 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Vinylogous acids Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Hydroxybenzaldehyde - Catechol - Benzoyl - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Benzenoid - Monocyclic benzene moiety - Vinylogous acid - Organic oxide - Hydrocarbon derivative - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as hydroxybenzaldehydes. These are organic aromatic compounds containing a benzene ring carrying an aldehyde group and a hydroxyl group.
External Descriptors	dihydroxybenzaldehyde
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	504756037
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504756037
IUPAC Name	2,3-dihydroxybenzaldehyde
INCHI	InChI=1S/C7H6O3/c8-4-5-2-1-3-6(9)7(5)10/h1-4,9-10H
InChIKey	IXWOUPGDGMCKGT-UHFFFAOYSA-N
Smiles	C1=CC(=C(C(=C1)O)O)C=O
Isomeric SMILES	C1=CC(=C(C(=C1)O)O)C=O
WGK Germany	3
Molecular Weight	138.12
Beilstein	2041781
Reaxy-Rn	2041781
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2041781&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

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12 results found

Lot Number	Certificate Type	Date	Item
K2426472	Certificate of Analysis	Nov 13, 2024	D122910
K2428308	Certificate of Analysis	Nov 13, 2024	D122910
K2426469	Certificate of Analysis	Nov 13, 2024	D122910
G2226361	Certificate of Analysis	Jun 15, 2022	D122910
G2226360	Certificate of Analysis	Jun 15, 2022	D122910
G2226362	Certificate of Analysis	Jun 15, 2022	D122910
C2412030	Certificate of Analysis	Jun 15, 2022	D122910
I1805080	Certificate of Analysis	Apr 27, 2022	D122910
K2101075	Certificate of Analysis	Nov 05, 2021	D122910
J2130490	Certificate of Analysis	Nov 05, 2021	D122910
K2101077	Certificate of Analysis	Nov 05, 2021	D122910
K2101076	Certificate of Analysis	Nov 05, 2021	D122910

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Chemical and Physical Properties

Solubility	Insoluble in water.
Sensitivity	air sensitive
Boil Point(°C)	120°C/16mmHg
Melt Point(°C)	107°C
Molecular Weight	138.120 g/mol
XLogP3	1.500
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	1
Exact Mass	138.032 Da
Monoisotopic Mass	138.032 Da
Topological Polar Surface Area	57.500 Å²
Heavy Atom Count	10
Formal Charge	0
Complexity	124.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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