| Identification | More | [Name]
3-CHLORO-2-METHYLPHENOL | [CAS]
3260-87-5 | [Synonyms]
3-CHLORO-2-METHYLPHENOL 3-chloro-o-cresol 3-Chloro-2-methylphenol 98% | [EINECS(EC#)]
221-861-0 | [Molecular Formula]
C7H7ClO | [MDL Number]
MFCD00079738 | [Molecular Weight]
142.58 | [MOL File]
3260-87-5.mol |
| Chemical Properties | Back Directory | [Melting point ]
86 °C | [Boiling point ]
225 °C | [density ]
1.1104 (rough estimate) | [refractive index ]
1.5449 (estimate) | [storage temp. ]
Inert atmosphere,Room Temperature | [form ]
powder | [pka]
9.35±0.10(Predicted) | [color ]
Brown | [Sensitive ]
Stench | [InChI]
1S/C7H7ClO/c1-5-6(8)3-2-4-7(5)9/h2-4,9H,1H3 | [InChIKey]
WADQOGCINABPRT-UHFFFAOYSA-N | [SMILES]
Cc1c(O)cccc1Cl | [CAS DataBase Reference]
3260-87-5(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi,Xn | [Risk Statements ]
R21/22:Harmful in contact with skin and if swallowed . R41:Risk of serious damage to eyes. R43:May cause sensitization by skin contact. R50:Very Toxic to aquatic organisms. R38:Irritating to the skin. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . S28:After contact with skin, wash immediately with plenty of ... (to be specified by the manufacturer) . | [RIDADR ]
3437 | [WGK Germany ]
WGK 3 | [HazardClass ]
IRRITANT, IRRITANT-HARMFUL | [HS Code ]
29081990 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Acute Tox. 4 Oral Aquatic Chronic 2 Eye Irrit. 2 |
| Hazard Information | Back Directory | [Synthesis]
1. In a 1000 mL three-necked flask equipped with a thermometer, a mechanical stirrer and a dropping funnel, 700 mL of 22% sulfuric acid solution was pre-filled and heated to 70 °C.
2. 8 g of 3-chloro-2-methylaniline was added to the above solution in batches, maintaining the temperature at 70 °C until completely dissolved.
3. The reaction mixture was heated to 90 °C and then cooled to 10-12 °C to form a suspension.
4. the diazotization reaction was carried out by slowly adding 88.4 g of 40% sodium nitrite solution dropwise under stirring, maintaining the temperature at 10-12 °C.
5. the resulting diazonium salt mixture was heated to 90 °C and then slowly added to a mixture containing 200 mL of methyl isobutyl ketone and 2 g of 96% sulfuric acid under vigorous stirring.
6. The reaction was held at 90 °C for about 15 minutes to complete, after which the emulsion was cooled to 70 °C for phase separation.
7. The organic phase was washed with 50 mL of water to remove inorganic impurities.
8. The selectivity of the thermal decomposition step was 99.1% (a/a) by gas chromatography (GC) analysis.
9. The organic phase was purified by distillation to give 66.9 g of 3-chloro-2-methylphenol with a GC purity of 99.2% (a/a).
10. The distillation residue was 2.3 g. The yield of the target product was calculated to be 93.1%. | [References]
[1] Patent: CN105392764, 2016, A. Location in patent: Paragraph 0026 [2] Patent: WO2007/39563, 2007, A1. Location in patent: Page/Page column 23-24 [3] Patent: US2007/112019, 2007, A1. Location in patent: Page/Page column 12/2 [4] Justus Liebigs Annalen der Chemie, 1906, vol. 350, p. 113 [5] Chemische Berichte, 1904, vol. 37, p. 1021 |
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