2-Hydroxy-4-nitrobenzaldehyde - ≥98% , CAS No.2460-58-4

CAS: 2460-58-4 Cat. No.: H588385 Molecular Weight: 167.12 EC Number: 219-549-4

GRADE & PURITY ≥98%

Synonyms

2-Hydroxy-4-nitrobenzaldehyde, AldrichCPR | 4-Nitrosalicylaldehyde | SY031966 | AKOS006223875 | Benzaldehyde,2-hydroxy-4-nitro- | W-206901 | UNII-94S8EF8NEF | SCHEMBL918368 | Salicylaldehyde, 4-nitro- | Benzaldehyde, 2-hydroxy-4-nitro- | AMY22947 | AE-562

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Synonyms

2-Hydroxy-4-nitrobenzaldehyde, AldrichCPR | 4-Nitrosalicylaldehyde | SY031966 | AKOS006223875 | Benzaldehyde, 2-hydroxy-4-nitro- | W-206901 | UNII-94S8EF8NEF | SCHEMBL918368 | Salicylaldehyde, 4-nitro- | Benzaldehyde, 2-hydroxy-4-nitro- | AMY22947 | AE-562

Specifications & Purity

≥98%

Storage

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.

Purity

≥98%

Names and Identifiers

• Canonical Smiles: C1=CC(=C(C=C1[N+](=O)[O-])O)C=O
• IUPAC Name: 2-hydroxy-4-nitrobenzaldehyde
• InChIKey: HHDPXULKSZZACU-UHFFFAOYSA-N
• INCHI: 1S/C7H5NO4/c9-4-5-1-2-6(8(11)12)3-7(5)10/h1-4,10H
• Isomeric SMILES: C1=CC(=C(C=C1[N+](=O)[O-])O)C=O
• Alternate CAS: 2460-58-4
• NSC Number: 82622
• MeSH Entry Terms: 4-nitrosalicylaldehyde
• Molecular Weight: 167.12
• Reaxy-Rn: 1103752
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1103752&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Class Benzene and substituted derivatives
      • Subclass Nitrobenzenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Benzene and substituted derivatives
• Subclass: Nitrobenzenes
• Intermediate Tree Nodes: Not available
• Direct Parent: Nitrobenzaldehydes
• Alternative Parents: Nitrophenols Hydroxybenzaldehydes Nitroaromatic compounds Benzoyl derivatives 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Vinylogous acids Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Nitrobenzaldehyde - Nitrophenol - Hydroxybenzaldehyde - Benzaldehyde - Nitroaromatic compound - Benzoyl - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Aryl-aldehyde - Vinylogous acid - C-nitro compound - Organic nitro compound - Organic oxoazanium - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organooxygen compound - Organonitrogen compound - Aldehyde - Organic oxide - Organopnictogen compound - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as nitrobenzaldehydes. These are nitrobenzenes that carry an aldehyde group at any position of the benzene ring.
• External Descriptors: Not available

Data sources

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

Chemical and Physical Properties

• Molecular Weight: 167.120 g/mol
• XLogP3: 2.000
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1
• Exact Mass: 167.022 Da
• Monoisotopic Mass: 167.022 Da
• Topological Polar Surface Area: 83.100 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 188.000
• 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

References

1. Selvaraj Muthusamy, Kanagaraj Rajalakshmi, Yeonggil Seo, Meng Xie, Palanisamy Kannan, Rathna Silviya Lodi, Jong-Won Song, Yuanguo Xu.  (2022)  Push-pull electronic effects on benzothiazole derived probes for the detection of Zn2+: Exploring the sensing strategies and its applications.  DYES AND PIGMENTS,      [PMID:] [10.1016/j.dyepig.2022.110709]