1,3-Dimethoxybenzene structure
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Common Name | 1,3-Dimethoxybenzene | ||
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CAS Number | 151-10-0 | Molecular Weight | 138.164 | |
Density | 1.0±0.1 g/cm3 | Boiling Point | 217.5±0.0 °C at 760 mmHg | |
Molecular Formula | C8H10O2 | Melting Point | -52°C | |
MSDS | Chinese USA | Flash Point | 87.8±0.0 °C |
Use of 1,3-Dimethoxybenzene1,3-Dimethoxybenzene belongs to the class of organic compounds known as dimethoxybenzenes. 1,3-Dimethoxybenzene is an intermediate in synthesis of organic compounds[1]. |
Name | 1,3-Dimethoxybenzene |
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Synonym | More Synonyms |
Description | 1,3-Dimethoxybenzene belongs to the class of organic compounds known as dimethoxybenzenes. 1,3-Dimethoxybenzene is an intermediate in synthesis of organic compounds[1]. |
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Related Catalog | |
References |
Density | 1.0±0.1 g/cm3 |
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Boiling Point | 217.5±0.0 °C at 760 mmHg |
Melting Point | -52°C |
Molecular Formula | C8H10O2 |
Molecular Weight | 138.164 |
Flash Point | 87.8±0.0 °C |
Exact Mass | 138.068085 |
PSA | 18.46000 |
LogP | 1.93 |
Vapour Pressure | 0.2±0.4 mmHg at 25°C |
Index of Refraction | 1.488 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Personal Protective Equipment | Eyeshields;Gloves;half-mask respirator (US);multi-purpose combination respirator cartridge (US) |
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Hazard Codes | Xi:Irritant |
Risk Phrases | R36/37/38 |
Safety Phrases | S24/25 |
RIDADR | NA 1993 / PGIII |
WGK Germany | 2 |
RTECS | CZ6474000 |
HS Code | 2909309090 |
Precursor 9 | |
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DownStream 10 | |
HS Code | 2909309090 |
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Summary | 2909309090 other aromatic ethers and their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0% |
Rotamers of o- and m-dimethoxybenzenes studied by mass-analyzed threshold ionization spectroscopy and theoretical calculations.
J. Phys. Chem. A 114(42) , 11144-52, (2010) We applied two-color resonant two-photon mass-analyzed threshold ionization (MATI) spectroscopy to investigate the molecular properties of the selected rotamers of o-dimethoxybenzene (ODMB) and m-dime... |
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Stereoselective glycosylations using oxathiane spiroketal glycosyl donors.
Carbohydr. Res. 348 , 6-13, (2012) Novel oxathiane spiroketal donors have been synthesised and activated via an umpolung S-arylation strategy using 1,3,5-trimethoxybenzene and 1,3-dimethoxybenzene. The comparative reactivity of the res... |
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Solvation of dichlorocarbene: complexation with aryl ethers.
J. Phys. Chem. A 114(1) , 209-17, (2010) Dichlorocarbene (CCl(2)), generated by laser flash photolysis of dichlorodiazirine, formed pi- and O-ylidic complexes with aromatic ethers such as anisole, 1,3-dimethoxybenzene, 1,3,5-trimethoxybenzen... |
dimethyl resorcinol |
FEMA 2385 |
Dimethylresorcinol,Resorcinol dimethyl ether |
M-METHOXYANISOLE |
Resorcinol Dimethyl Ether |
EINECS 205-783-4 |
m-dimethoxy-benzen |
3-METHOXYANISOLE |
1,3-Dimethoxybenzene |
2,4-dimethoxy-benzene |
meta-dimethoxybenzene |
M-DIMETHOXYBENZENE |
MFCD00008384 |
2,6-dimethoxybenzene |
1,3-methoxybenzenel |
Benzene, 1,3-dimethoxy- |
1,3-Dimethoxybenzol |
1,3-dimethoxy benzene |
Resorcin-dimethylether |
3-DiMethoxybenzene |
Dimethylresorinol |
m-Dimethoxy benzene |