122017
o-Toluoyl chloride
99%
Synonym(s):
2-Methylbenzoyl chloride
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About This Item
Linear Formula:
CH3C6H4COCl
CAS Number:
Molecular Weight:
154.59
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
99%
refractive index
n20/D 1.5549 (lit.)
bp
88-90 °C/12 mmHg (lit.)
density
1.185 g/mL at 25 °C (lit.)
SMILES string
Cc1ccccc1C(Cl)=O
InChI
1S/C8H7ClO/c1-6-4-2-3-5-7(6)8(9)10/h2-5H,1H3
InChI key
GPZXFICWCMCQPF-UHFFFAOYSA-N
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General description
Flash vacuum pyrolysis of o-toluoyl chloride at 780°C and 0.5 mmHg yields benzocyclobutenone.
Application
- Development of hydrophobic functionalized materials: o-Toluoyl chloride was utilized in the synthesis of novel hydrophobic functionalized UiO-66 materials. The study demonstrated the chemical′s role in enhancing the structural and physicochemical properties of these metal-organic frameworks, indicating potential applications in catalysis and adsorption processes (Narea et al., 2023).
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
WGK
WGK 3
Flash Point(F)
170.6 °F
Flash Point(C)
77 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Certificates of Analysis (COA)
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Improved synthesis of benzocyclobutenone by flash vacuum pyrolysis.
Suzzarini L, et al.
Tetrahedron Letters, 39(13), 1695-1696 (1998)
Ataf Ali Altaf et al.
Dalton transactions (Cambridge, England : 2003), 47(34), 11769-11781 (2018-08-18)
Twenty-three compounds in two series of ferrocene-based anilides, with the general formula C5H5-Fe-C5H4-C6H4-NH-CO-C6H4-R (where R = H, F, Cl, CH3 and OCH3), have been successfully synthesized. The compounds were characterized by elemental analysis and FTIR, 1H NMR and 13C NMR
Shigeo Hayashi et al.
Journal of enzyme inhibition and medicinal chemistry, 29(6), 846-867 (2014-02-13)
Because of the pivotal role of cyclooxygenase (COX) in the inflammatory processes, non-steroidal anti-inflammatory drugs (NSAIDs) that suppress COX activities have been used clinically for the treatment of inflammatory diseases/syndromes; however, traditional NSAIDs exhibit serious side-effects such as gastrointestinal damage
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