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Quality Level
Assay
97%
form
solid
bp
290 °C (lit.)
mp
75-77 °C (lit.)
functional group
ester
SMILES string
COC(=O)c1ccc2ccccc2c1
InChI
1S/C12H10O2/c1-14-12(13)11-7-6-9-4-2-3-5-10(9)8-11/h2-8H,1H3
InChI key
IODOXLXFXNATGI-UHFFFAOYSA-N
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Cucurbit [8] uril-mediated photodimerization of alkyl 2-naphthoate in aqueous solution.
Tetrahedron Letters, 49(9), 1502-1505 (2008)
Molecular association of singlet excited state methyl 2-naphthoate; effects of excimer formation on photocycloaddition.
Research on Chemical Intermediates, 19(3), 191-209 (1993)
Stereochemistry of a cubane-like photodimer of methyl 2-naphthoate.
Tetrahedron Letters, 47(27), 4725-4727 (2006)
Photochemical synthesis. VI. The formation of benzosemibullvalene derivatives in the photoaddition of diphenylacetylene to methyl 2-naphthoate, a degenerate thermal isomerization of the benzosemibullvalene skeleton.
Australian Journal of Chemistry, 26(1), 147-171 null
Journal of mass spectrometry : JMS, 53(5), 379-384 (2018-02-15)
Gas phase decompositions of protonated methyl benzoate and its conjugates have been studied by using electrospray ionization-collision induced dissociation-tandem mass spectrometry. Loss of CO2 molecule, thus transfer of methyl group, has been observed. In order to better understand this process
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