Name | Methyl 3-nitrobenzoate |
Synonyms | AKOS B029800 RARECHEM AL BF 0189 Methyl 3-nitrobenzoate 4-Methyl-3-nitrobenzoate Methyl meta-nitrobenzoate Methyl 3-Nitrobenzoic Acid 3-nitro-benzoicacimethylester Benzoicacid,3-nitro-,methylester 3-Nitrobenzoic acid methyl ester m-Nitrobenzoic acid, methyl ester Benzoic acid, m-nitro-, methyl ester Benzoic acid, 3-nitro-, methyl ester |
CAS | 618-95-1 |
EINECS | 210-573-0 |
InChI | InChI=1/C8H7NO4/c1-13-8(10)6-3-2-4-7(5-6)9(11)12/h2-5H,1H3 |
InChIKey | AXLYJLKKPUICKV-UHFFFAOYSA-N |
Molecular Formula | C8H7NO4 |
Molar Mass | 181.15 |
Density | 1.4283 (rough estimate) |
Melting Point | 78-80 °C (lit.) |
Boling Point | 279 °C (lit.) |
Flash Point | 279°C |
Water Solubility | insoluble |
Vapor Presure | 0.00293mmHg at 25°C |
Appearance | Crystalline Powder |
Color | Beige |
BRN | 392449 |
Storage Condition | Sealed in dry,Room Temperature |
Stability | Stable. Incompatible with strong oxidizing agents. |
Refractive Index | 1.5468 (estimate) |
Physical and Chemical Properties | White needle-like crystals. The melting point of 78 deg C, boiling point of 279 deg C. Slightly soluble in ethanol, ether, methanol, insoluble in water. |
Use | Used as an intermediate in organic synthesis |
Safety Description | 24/25 - Avoid contact with skin and eyes. |
WGK Germany | 3 |
TSCA | Yes |
HS Code | 29163900 |
NIST chemical information | information provided by: webbook.nist.gov (external link) |
EPA chemical substance information | information provided by: ofmpeb.epa.gov (external link) |
Use | for organic synthesis. used as intermediate in organic synthesis |
production method | is obtained by nitration of methyl benzoate. The concentrated sulfuric acid was added into the dry reaction Pan, cooled to 0-10 °c, methyl benzoate was slowly added, and then the mixture of fuming nitric acid and concentrated sulfuric acid was added dropwise, and the temperature was controlled to 5-15 °c. After addition, the reaction was carried out at 15 °c for 1H. Cooling, adding ice precipitation of M-nitrobenzoic acid methyl ester. After filtration, the oily substance was washed with alcohol and washed with water to obtain a finished product. The yield was 80%. |