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Factory supply 3,5-Dimethoxytoluene 4179-19-5 with low price
- Molecular Formula: C9H12O2
- Molecular Weight: 152.193
- Appearance/Colour: Clear colorless to yellow liquid
- Vapor Pressure: 0.0486mmHg at 25°C
- Melting Point: 61-62 °C
- Refractive Index: n20/D 1.522(lit.)
- Boiling Point: 244 °C at 760 mmHg
- Flash Point: 87.5 °C
- PSA: 18.46000
- Density: 0.99 g/cm3
- LogP: 2.01220
3,5-Dimethoxytoluene(Cas 4179-19-5) Usage
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Synthesis Reference(s) |
Organic Syntheses, Coll. Vol. 6, p. 859, 1988The Journal of Organic Chemistry, 70, p. 3275, 2005 DOI: 10.1021/jo050075r |
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General Description |
3,5-Dimethoxytoluene (DMT) is a methoxylated phenolic derivative. It is reported to be one of the main constituent of the floral volatiles in different rose varieties. It has been biosynthesized from orcinol by two successive methylation catalyzed by O-methyltransferases (OMTs). The features of its aerobic oxidation with metal/bromide catalysts have been investigated. |
InChI:InChI=1/C9H12O2/c1-7-4-8(10-2)6-9(5-7)11-3/h4-6H,1-3H3
4179-19-5 Relevant articles
Organochlorine compounds from a terrestrial higher plant: Structures and origin of chlorinated orcinol derivatives from diseased bulbs of Lilium maximowiczii
Monde, Kenji,Satoh, Hikari,Nakamura, Masao,Tamura, Mamoru,Takasugi, Mitsuo
, p. 913 - 921 (1998)
Seven chlorine-containing orcinol deriva...
An Asymmetric Synthesis of Hamigeran B via a Pd Asymmetric Allylic Alkylation for Enantiodiscrimination
Trost, Barry M.,Pissot-Soldermann, Carole,Chen, Irwin,Schroeder, Gretchen M.
, p. 4480 - 4481 (2004)
A protocol for the asymmetric allylic al...
Radical induced disproportionation of alcohols assisted by iodide under acidic conditions
Huang, Yang,Jiang, Haiwei,Li, Teng,Peng, Yang,Rong, Nianxin,Shi, Hexian,Yang, Weiran
supporting information, p. 8108 - 8115 (2021/10/29)
The disproportionation of alcohols witho...
Metal-Free Heterogeneous Semiconductor for Visible-Light Photocatalytic Decarboxylation of Carboxylic Acids
Shi, Jiale,Yuan, Tao,Zheng, Meifang,Wang, Xinchen
, p. 3040 - 3047 (2021/03/09)
A suitable protocol for the photocatalyt...
Molybdenum-Catalyzed Deoxygenation Coupling of Lignin-Derived Alcohols for Functionalized Bibenzyl Chemicals
Jiang, Huifang,Lu, Rui,Luo, Xiaolin,Si, Xiaoqin,Xu, Jie,Lu, Fang
supporting information, p. 1292 - 1296 (2020/12/09)
With the growing demand for sustainabili...
Method for hydrogenolysis of halides
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Paragraph 0232; 0296-0298, (2021/01/11)
The invention discloses a method for hyd...
4179-19-5 Process route
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504-15-4
orcinol
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74-88-4
methyl iodide
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3209-13-0
O-methylorcinol
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4179-19-5
1,3-dimethoxy-5-methylbenzene
| Conditions | Yield |
|---|---|
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With
methanol; potassium hydroxide;
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504-15-4
orcinol
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67-56-1
methanol
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74-88-4
methyl iodide
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-
3209-13-0
O-methylorcinol
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-
4179-19-5
1,3-dimethoxy-5-methylbenzene
| Conditions | Yield |
|---|---|
|
|
4179-19-5 Upstream products
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504-15-4
orcinol
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77-78-1
dimethyl sulfate
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3209-13-0
O-methylorcinol
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74-88-4
methyl iodide
4179-19-5 Downstream products
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854678-27-6
4-(2,4-dimethoxy-6-methyl-phenyl)-4-oxo-butyric acid
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20872-08-6
2,6-dimethoxy-4-methylbenzoic acid
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7149-90-8
2,4-dimethoxy-6-methyl-benzaldehyde
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855890-69-6
1-(2-hydroxy-4-methoxy-6-methyl-phenyl)-heptadecan-1-one