ChemicalBook--->CAS DataBase List--->3587-64-2

3587-64-2

3587-64-2 Structure

3587-64-2 Structure
IdentificationBack Directory
[Name]

1-METHOXY-2-METHYL-2-PROPANOL
[CAS]

3587-64-2
[Synonyms]

2-(Methoxymethyl)-2-propanol
2-(Methoxymethyl)propane-2-ol
2-Methoxy-1,1-dimethylethanol
1-METHOXY-2-METHYL-2-PROPANOL
1-METHOXY-2-METHYLPROPAN-2-OL
1,1-Dimethyl-2-methoxyethanol
1-Methoxy-2-methylpropane-2-ol
2-Propanol, 1-methoxy-2-methyl-
1-METHOXY-2-METHYL-2-PROPANOL, 99+%
1-METHOXY-2-METHYL-2-PROPANOL, 98+%
1-Methoxy-2-methyl-2-propanol, AcroSeal, 98%
1-Methoxy-2-Methyl-2-propanol, 98%, AcroSeal
1-Methoxy-2-methyl-2-propanol, 98%, AcroSeal&trade
[EINECS(EC#)]

609-188-4
[Molecular Formula]

C5H12O2
[MDL Number]

MFCD03701584
[MOL File]

3587-64-2.mol
[Molecular Weight]

104.15
Chemical PropertiesBack Directory
[Boiling point ]

115-116 °C(lit.)
[density ]

0.892 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.4044(lit.)
[Fp ]

82 °F
[storage temp. ]

2-8°C
[form ]

Liquid
[pka]

14.56±0.29(Predicted)
[color ]

Clear colorless
[LogP]

0.069 (est)
[CAS DataBase Reference]

3587-64-2
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

10-36/37/38
[Safety Statements ]

26-36
[RIDADR ]

UN 1987 3/PG 3
[WGK Germany ]

3
[HazardClass ]

3
[PackingGroup ]

III
[HS Code ]

29094980
Spectrum DetailBack Directory
[Spectrum Detail]

1-METHOXY-2-METHYL-2-PROPANOL(3587-64-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

Isobutylene oxide

558-30-5

Methanol

67-56-1

1-METHOXY-2-METHYL-2-PROPANOL

3587-64-2

1. Catalyst pretreatment: 0.037 mmol of Zr catalyst was added to a 25 mL round-bottomed flask and heated at 150°C under vacuum overnight to remove the absorbed water. 2. Reaction system preparation: 5mL of methanol was added to the flask and sonicated for 15 min. 3. Addition of reactants: 1 mmol of propylene oxide was added. 4. 4. Reaction condition setting: Place the reaction mixture in a bath preheated to 50°C with magnetic stirring. 5. Catalyst activation (if applicable): 2.5 mL of acetone was added as solvent and after sonication of the catalyst, 1.0 mmol of amine and 1.0 mmol of styrene oxide were added sequentially. 6. Reaction termination and product recovery: At the end of the reaction, the catalyst was washed thoroughly with methanol to recover the adsorbed products. 7. Product purification: The product was purified using silica gel. 7. Product purification: The product was purified by rapid column chromatography using silica gel column chromatography with hexane:methylene chloride as eluent. 8. Reaction monitoring: Aliquots of the reaction mixture were withdrawn periodically with a syringe, diluted with methanol and immediately analyzed by GC (Agilent 6890 network GC system), and the product concentration was determined by a calibration curve.

[References]

[1] Journal of Molecular Catalysis A: Chemical, 2016, vol. 425, p. 332 - 339
[2] Patent: US2886600, 1957,
[3] Journal of Molecular Structure, 1991, vol. 243, p. 111 - 122
[4] Patent: US2886600, 1957,
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