5-Methyl-1,3-benzodioxol
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- CAS-Nr.
- 7145-99-5
- Bezeichnung:
- 5-Methyl-1,3-benzodioxol
- Englisch Name:
- 5-METHYL-1,3-BENZODIOXOLE
- Synonyma:
- ai3-20481;TIMTEC-BB SBB008152;5-methyl-3-benzodioxole;5-METHYL-1,3-BENZODIOXOLE;3,4-methylenedioxy-toluen;1,3-Benzodioxole, 5-methyl-;3,4-(METHYLENEDIOXY)TOLUENE;5-Methylbenzo[d][1,3]dioxole;4-METHYL-1,2-METHYLENEDIOXYBENZENE;1,2-(Methylenedioxy)-4-methylbenzene
- CBNumber:
- CB0438748
- Summenformel:
- C8H8O2
- Molgewicht:
- 136.15
- MOL-Datei:
- 7145-99-5.mol
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5-Methyl-1,3-benzodioxol Eigenschaften
- Siedepunkt:
- 199-200 °C (lit.)
- Dichte
- 1.135 g/mL at 25 °C (lit.)
- Brechungsindex
- n20/D 1.532(lit.)
- Flammpunkt:
- 169 °F
- storage temp.
- 2-8°C
- CAS Datenbank
- 7145-99-5(CAS DataBase Reference)
5-Methyl-1,3-benzodioxol Chemische Eigenschaften,Einsatz,Produktion Methoden
Verwenden
3,4-(Methylenedioxy)toluene can be used as a cation scavenger for the selective cleavage of 4-(3,4-dimethoxyphenyl)benzyl (DMPBn) ethers affording the corresponding deprotected products in the presence of trifluoroacetic acid (TFA) in anhydrous CH
2Cl
2.
It can also be used as a starting material to prepare:
- 1,3-Benzodioxole-5-carboxaldehyde via photooxidation using CBr4.
- 6-Methyl-1,3-benzodioxole-5-carboxaldehyde by treating with dichloromethylmethyl ether and TiCl4.
5-Methyl-1,3-benzodioxol Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
5-Methyl-1,3-benzodioxol Anbieter Lieferant Produzent Hersteller Vertrieb Händler.
Global( 87)Lieferanten
7145-99-5(5-Methyl-1,3-benzodioxol)Verwandte Suche:
- TIMTEC-BB SBB008152
- 4-METHYL-1,2-METHYLENEDIOXYBENZENE
- 5-METHYL-1,3-BENZODIOXOLE
- 3,4-(METHYLENEDIOXY)TOLUENE
- 1,3-Benzodioxole, 5-methyl-
- 3,4-methylenedioxy-toluen
- 5-methyl-3-benzodioxole
- ai3-20481
- 5-Methyl-1,3-benzodioxole~1-Methyl-3,4-(methylenedioxy)benzene
- 1,2-(Methylenedioxy)-4-methylbenzene
- 5-Methylbenzo[d][1,3]dioxole
- 7145-99-5
- Building Blocks
- Organic Building Blocks
- Oxygen Compounds
- Protected Alcohols/Phenols
- Building Blocks
- Chemical Synthesis
- Organic Building Blocks
- Oxygen Compounds
- Protected Alcohols/Phenols
- Aromatic Hydrocarbons (substituted) & Derivatives