2,4-Dimethylbenzaldehyde - ≥95% , CAS No.15764-16-6

CAS: 15764-16-6 Cat. No.: D103125 Molecular Weight: 134.18 Beilstein Registry Number: 7310 EC Number: 239-856-7

GRADE & PURITY ≥95%

Synonyms

2,4-Dimethylbenzaldehyde, >=90% | DS-15791 | I06YU18H4A | STL185603 | UNII-I06YU18H4A | 2,3-Dimethybenzaldehyde | MFCD00003340 | 1-Formyl-2,4-dimethylbenzene | DTXSID60166297 | Q27280189 | 2,4-Dimethylbenzaldehyde, Vetec(TM) reagent grade, 95% | 2,4-DIMET

Storage

Argon charged,Room temperature

Shipped In

Normal

Specifications

Synonyms

2, 4-Dimethylbenzaldehyde, >=90% | DS-15791 | I06YU18H4A | STL185603 | UNII-I06YU18H4A | 2, 3-Dimethybenzaldehyde | MFCD00003340 | 1-Formyl-2, 4-dimethylbenzene | DTXSID60166297 | Q27280189 | 2, 4-Dimethylbenzaldehyde, Vetec(TM) reagent grade, 95% | 2, 4-DIMET

Specifications & Purity

≥95%

Storage

Argon charged, Room temperature

Shipped In

Normal

Purity

≥95%

Names and Identifiers

• Pubchem Sid: 488183533
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488183533
• Canonical Smiles: CC1=CC(=C(C=C1)C=O)C
• IUPAC Name: 2,4-dimethylbenzaldehyde
• InChIKey: GISVICWQYMUPJF-UHFFFAOYSA-N
• INCHI: 1S/C9H10O/c1-7-3-4-9(6-10)8(2)5-7/h3-6H,1-2H3
• Isomeric SMILES: CC1=CC(=C(C=C1)C=O)C
• WGK Germany: 3
• Molecular Weight: 134.18
• Beilstein: 7310
• Reaxy-Rn: 507131
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=507131&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Benzene and substituted derivatives
• Subclass: Benzoyl derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzoyl derivatives
• Alternative Parents: m-Xylenes Benzaldehydes Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: M-xylene - Xylene - Benzoyl - Benzaldehyde - Aryl-aldehyde - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aldehyde - Aromatic homomonocyclic compound
• Description: This compound belongs to the class of organic compounds known as benzoyl derivatives. These are organic compounds containing an acyl moiety of benzoic acid with the formula (C6H5CO-).
• 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

• Sensitivity: Air sensitive.
• Refractive Index: 1.549
• Flash Point(°F): 192.2 °F
• Flash Point(°C): 89 °C
• Boil Point(°C): 102-103°C/14mmHg
• Melt Point(°C): -9°C
• Molecular Weight: 134.170 g/mol
• XLogP3: 2.500
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 134.073 Da
• Monoisotopic Mass: 134.073 Da
• Topological Polar Surface Area: 17.100 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 120.000
• 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. Siyue Liu, Jinge Xie, Wenqi Luan, Chen Liu, Xiwen Chen, Defu Chen.  (2024)  Papiliotrema flavescens, a plant growth-promoting fungus, alters root system architecture and induces systemic resistance through its volatile organic compounds in Arabidopsis.  PLANT PHYSIOLOGY AND BIOCHEMISTRY,      [PMID:38430787] [10.1016/j.plaphy.2024.108474]

2. Bo Zeng, Shuiping Ouyang, Zhaoxiang Wang, Shixiu Cui, Guocheng Du, Song Liu.  (2026)  Ancestral bacterial laccase enables efficient biodetoxification of inhibitory wheat straw hydrolysate for sustainable microbial protein production.  GREEN CHEMISTRY,      [PMID:] [10.1039/D5GC05697G]