- 2,4-Dimethylpyrrole
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- $0.00 / 200KG
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2025-06-27
- CAS:625-82-1
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 500000kg
- 2,4-Dimethylpyrrole
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- $0.00 / 1kgkg
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2025-06-20
- CAS:625-82-1
- Min. Order: 1kgkg
- Purity: 0.99
- Supply Ability: 1000kg
- 2,4-Dimethylpyrrole
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- $80.00 / 1kg
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2025-06-03
- CAS:625-82-1
- Min. Order: 10kg
- Purity: 0.99
- Supply Ability: 20tons
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| | 2,4-Dimethylpyrrole Basic information |
| Product Name: | 2,4-Dimethylpyrrole | | Synonyms: | Pyrrole, 2,4-dimethyl-;pyrrole,2,4-dimethyl-;2,4-DIMETHYLPYRROLE;2,4-DIMETHYL-1H-PYRROLE;2,4-Dimethylpyrrole 98%;1H-Pyrrole, 2,4-dimethyl-;2,4-Dimethylpyrrole,97%;2,4-Dimethylpyrrole ,98% | | CAS: | 625-82-1 | | MF: | C6H9N | | MW: | 95.14 | | EINECS: | 210-912-2 | | Product Categories: | Imidazoles, Pyrroles, Pyrazoles, Pyrrolidines;Building Blocks;Heterocyclic Building Blocks;Pyrroles;Pharmaceutial intermediates;Heterocycles;bc0001;625-82-1 | | Mol File: | 625-82-1.mol |  |
| | 2,4-Dimethylpyrrole Chemical Properties |
| Melting point | 6.5°C (estimate) | | Boiling point | 165-167 °C (lit.) | | density | 0.924 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.496(lit.) | | Fp | >230 °F | | storage temp. | Keep in dark place,Inert atmosphere,2-8°C | | solubility | Chloroform (Slightly), Methanol (Slightly) | | pka | 18.03±0.50(Predicted) | | form | Crystalline Powder | | color | Orange-red to maroon, brown or violet | | Stability: | Light Sensitive | | InChI | 1S/C6H9N/c1-5-3-6(2)7-4-5/h3-4,7H,1-2H3 | | InChIKey | MFFMQGGZCLEMCI-UHFFFAOYSA-N | | SMILES | Cc1c[nH]c(C)c1 | | LogP | 1.667 (est) | | CAS DataBase Reference | 625-82-1(CAS DataBase Reference) | | NIST Chemistry Reference | 1H-Pyrrole, 2,4-dimethyl-(625-82-1) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36-37/39 | | WGK Germany | 3 | | HS Code | 29339900 | | Storage Class | 10 - Combustible liquids | | Hazard Classifications | Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| | 2,4-Dimethylpyrrole Usage And Synthesis |
| Chemical Properties | clear light yellow to light yellow-orange liquid | | Uses | 2,4-Dimethylpyrrole is a substituted pyrrole. Its synthesis by using ethyl acetoacetate as starting material has been reported. Its basicity has been evaluated from UV spectral data.Its photodecomposition on irradiation has been reported to afford H2, CH4, C2H6 and polymeric products.
2,4-Dimethylpyrrole may be used in the synthesis of the following:
2,5-bis(2′,4′-dimethyl-5′-pyrryl)p-benzoquinone.
boron dipyrromethene (BODIPY) dyes.
2,4-dimethyl-6-methoxyprodigiosene. | | Uses | 2,4-Dimethylpyrrole may be used in the synthesis of the following:
- 2,5-bis(2′,4′-dimethyl-5′-pyrryl)p-benzoquinone
- boron dipyrromethene (BODIPY) dyes
- 2,4-dimethyl-6-methoxyprodigiosene
| | Synthesis Reference(s) | Synthesis, p. 1585, 2000 DOI: 10.1055/s-2000-7618 | | General Description | 2,4-Dimethylpyrrole is a substituted pyrrole. Its synthesis by using ethyl acetoacetate as starting material has been reported. Its basicity has been evaluated from UV spectral data. Its photodecomposition on irradiation has been reported to afford H2, CH4, C2H6 and polymeric products. | | Synthesis | 420 g (2.0 mol) of 2,4-dimethyl-3,5-bismethoxycarbonylpyrrole were suspended in 1200 g of 20% strength sodium hydroxide solution, and the mixture was heated. The solid gradually passed into solution during this process. At 92° C. gas had started to evolve vigorously; some of the dicarboxylic acid was decarboxylated in the process. The methanol formed during the hydrolysis was distilled off continuously until essentially only water was passing over. The mixture which remained was then neutralized with 250 g of 50% strength sulfuric acid (pH about 7.5) and heated to boiling at the reflux condenser with water separator. The 2,4-dimethylpyrrole separated out as a yellow upper phase over the course of a few hours. The aqueous phase was continuously recycled into the boiling mixture. A total of 152.5 g of organic phase was obtained. This comprised 8.1% of water, the remainder consisted of 99.1% of 2,4-dimethylpyrrole, determined as area percentages by gas chromatography using a flame ionization detector. This corresponded to 138.9 g of 2,4-dimethylpyrrole (73% of theory). |
| | 2,4-Dimethylpyrrole Preparation Products And Raw materials |
| Raw materials | 4-Isopropylidene-3-methyl-4H-isoxazol-5-one-->2,4-DiforMylpyrrole-->2-hydroxyethyl formate-->4-TERT-BUTYL-3,5-DIMETHYL-1H-PYRROLE-2-CARBOXYLIC ACID ETHYL ESTER-->1,2,5-TRIMETHYLPYRROLE-->2-CHLORO-4-NITROBENZOYL CHLORIDE-->Ethanone, 1-(1,2,5-trimethyl-1H-pyrrol-3-yl)- (9CI)-->3,5-Dimethyl-1H-pyrrole-2,4-dicarboxylic acid-->3-Acetyl-2,4-dimethylpyrrole-->Ethyl 3,5-dimethyl-1H-pyrrole-2-carboxylate-->Diethyl 2,4-dimethylpyrrole-3,5-dicarboxylate-->2,5-Dimethyl-1H-pyrrole-->tert-Butyl acetate-->Acetone oxime | | Preparation Products | BODIPY-->3,5-Dimethyl-1H-pyrrole-2-carboxaldehyde |
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