1,2-Dimethoxybenzene

From Wikipedia, the free encyclopedia
  (Redirected from 1,2-dimethoxybenzene)
Jump to: navigation, search
1,2-Dimethoxybenzene
1,2-Dimethoxybenzene
1,2-Dimethoxybenzene molecule
Names
IUPAC name
1,2-Dimethoxybenzene
Other names
Veratrole
o-Dimethoxybenzene
Pyrocatechol dimethyl ether
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.001.860
UNII
Properties
C8H10O2
Molar mass 138.17 g·mol−1
Density 1.084 g/cm3[1]
Melting point 22–23 °C (72–73 °F; 295–296 K) [1]
Boiling point 206–207 °C (403–405 °F; 479–480 K) [1]
-87.39·10−6 cm3/mol
Hazards
NFPA 704
Flammability code 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g., diesel fuel Health code 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g., chloroform Reactivity (yellow): no hazard code Special hazards (white): no codeNFPA 704 four-colored diamond
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

1,2-Dimethoxybenzene, commonly known as veratrole, is an organic compound with the formula C6H4(OCH3)2. It is a colorless liquid, with a pleasant odor and slight solubility in water. It is the dimethyl ether derived from pyrocatechol.

Occurrence[edit]

1,2-Dimethoxybenzene is naturally occurring. Its biosynthesis entails the methylation of guaiacol by guaiacol O-methyltransferase.[2] 1,2-Dimethoxybenzene is an insect attractant.[2] Guaiacol O-methyltransferase gene is first scent gene discovered so far in any plant species.[2]

Uses[edit]

1,2-Dimethoxybenzene is a building block for the organic synthesis of other aromatic compounds. Veratrole is relatively electron-rich and thus readily undergoes electrophilic substitution.[3]

An example of the use of veratrole is in the synthesis of Domipizone.[4]

Veratrole can easily be brominated with NBS to give 4-bromoveratrole.[5]

Related compounds[edit]

References[edit]

  1. ^ a b c Merck Index, 11th Edition, 9857
  2. ^ a b c Gupta, Alok K; Akhtar, Tariq A; Widmer, Alex; Pichersky, Eran; Schiestl, Florian P (2012). "Identification of white campion (Silene latifolia) guaiacol O-methyltransferase involved in the biosynthesis of veratrole, a key volatile for pollinator attraction". BMC Plant Biology. 12: 158. doi:10.1186/1471-2229-12-158. PMC 3492160Freely accessible. PMID 22937972. 
  3. ^ Janssen, D. E.; Wilson, C. V. (1963). "4-Iodoveratrole". Organic Syntheses. ; Collective Volume, 4, p. 547 
  4. ^ EP 0129791 , (1985); CA, 102, 220886 (synth, pharmacol).
  5. ^ Bannard, R. A. B.; Latremouille, G. (1953). "4-BROMOVERATROLE". Canadian Journal of Chemistry. 31 (4): 469–469. doi:10.1139/v53-062. ISSN 0008-4042.