Name | 2,4-Dimethoxybenzonitrile |
Synonyms | 2,4-Dimethoxybenzoni 2,4 methoxybenzonitrile 2,4-Dimethoxybenzonitrile 2,4 Dimethoxybenxonitrile 2,4-DIMETHOXYBENZONITRILE Benzonitrile, 2,4-dimethoxy- |
CAS | 4107-65-7 |
EINECS | 223-886-2 |
InChI | InChI=1/C9H9NO2/c1-11-8-4-3-7(6-10)9(5-8)12-2/h3-5H,1-2H3 |
InChIKey | RYRZSQQELLQCMZ-UHFFFAOYSA-N |
Molecular Formula | C9H9NO2 |
Molar Mass | 163.17 |
Density | 1.2021 (rough estimate) |
Melting Point | 93-94 °C (lit.) |
Boling Point | 290.25°C (rough estimate) |
Flash Point | 128.8°C |
Vapor Presure | 0.000758mmHg at 25°C |
Appearance | Solid |
Color | White to slightly yellow |
BRN | 1950512 |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | 1.5300 (estimate) |
MDL | MFCD00001786 |
Risk Codes | R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed. R36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. S36/37 - Wear suitable protective clothing and gloves. |
UN IDs | 3276 |
WGK Germany | 3 |
HS Code | 29269095 |
Hazard Class | 6.1 |
Packing Group | III |
properties | white to light yellow crystalline powder |
uses | benzonitrile is an important organic intermediate, mainly used in the preparation of medicines and pesticides, it is widely used in the manufacturing process of dyes, engineering plastics and photosensitive materials. |
preparation | traditional methods for synthesizing halobenzonitrile include photo-halogenation, ammonia oxidation, phase transfer catalytic synthesis or reaction of carboxylic acid and urea, etc. In this paper, substituted benzaldehyde is used as the starting material, and then 2, 4-dimethoxybenzaldehyde oxime is formed, and then oxime is dehydrated with hydroxylamine to obtain substituted benzonitrile. Although there are many steps in this route, the yield of each step is higher, and the product is easy to separate and purify, which is a feasible route. The synthesis reaction formula of 2, 4-dimethoxybenzonitrile is as follows: Figure 1 2, the synthesis reaction formula of 4-dimethoxybenzonitrile |