Introduction：Basic information about 4-Methyl-3-nitroanisole CAS 17484-36-5, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
4-Methyl-3-nitroanisole Basic information
| Product Name: | 4-Methyl-3-nitroanisole |
| Synonyms: | TIMTEC-BB SBB008488;4-METHYL-3-NITROANISOLE;4-METHOXY-1-METHYL-2-NITRO-BENZENE;4-METHOXY-2-NITROTOLUENE;2-Nitro-4-methoxytoluene;Anisole, 4-methyl-3-nitro-;4-METHYL-3-NITROANISOLE 99%;1-Methyl-2-nitro-4-methoxybenzene |
| CAS: | 17484-36-5 |
| MF: | C8H9NO3 |
| MW: | 167.16 |
| EINECS: | 241-500-0 |
| Product Categories: | Aromatic Ethers;Aromatics Compounds;Phenyls & Phenyl-Het;Anisole;Aromatics;Phenyls & Phenyl-Het |
| Mol File: | 17484-36-5.mol |
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4-Methyl-3-nitroanisole Chemical Properties
| Melting point | 17 °C (lit.) |
| Boiling point | 266-267 °C (lit.) |
| density | 1.207 g/mL at 25 °C (lit.) |
| refractive index | n20/D 1.552(lit.) |
| Fp | >230 °F |
| storage temp. | Sealed in dry,Room Temperature |
| solubility | Chloroform |
| form | Light Yellow Liquid |
| Appearance | Light yellow to yellow Liquid |
| Water Solubility | insoluble |
| BRN | 2047309 |
| InChI | 1S/C8H9NO3/c1-6-3-4-7(12-2)5-8(6)9(10)11/h3-5H,1-2H3 |
| InChIKey | JBORNNNGTJSTLC-UHFFFAOYSA-N |
| SMILES | COc1ccc(C)c(c1)[N+]([O-])=O |
| CAS DataBase Reference | 17484-36-5(CAS DataBase Reference) |
| NIST Chemistry Reference | Benzene, 4-methoxy-1-methyl-2-nitro-(17484-36-5) |
Safety Information
| Hazard Codes | Xn,Xi |
| Risk Statements | 22-36/37/38 |
| Safety Statements | 24/25-36-26 |
| WGK Germany | 3 |
| Hazard Note | Harmful |
| HS Code | 29093090 |
| Storage Class | 10 - Combustible liquids |
| Hazard Classifications | Acute Tox. 4 Oral
Eye Irrit. 2 |
4-Methyl-3-nitroanisole Usage And Synthesis
| Chemical Properties | Light Yellow Liquid |
| Uses | 4-Methyl-3-nitroanisole (cas# 17484-36-5) is a compound useful in organic synthesis. |
| Uses | 4-Methyl-3-nitroanisole was used as external standard in synthesis of antibody catalysts by bait and switch hapten strategy. It was used as starting material for synthesis of 4-fluoro and 2-fluoro-substituted acetylcholinesterase inhibitors. |
4-Methyl-3-nitroanisole Preparation Products And Raw materials
| Raw materials | Potassium carbonate-->Acetonitrile-->Dimethyl sulfate-->Glycine-->4-Methyl-3-nitrophenol |
| Preparation Products | 4-Methoxy-2-nitrobenzoic acid-->2-hydroxy-4-Methoxytoluene-->4-Methyl-2-nitroanisole-->2-AMINO-P-ANISIC ACID HYDROCHLORIDE |
