2-METHYL-2-PROPAN(OL-D)
2-METHYL-2-PROPAN(OL-D) Basic information
- Product Name:
- 2-METHYL-2-PROPAN(OL-D)
- Synonyms:
-
- TERT-BUTAN-OL-D 98 PLUS ATOM % D
- 2-METHYL-2-PROPAN(OL-D) 99 ATOM % D
- tert-Butanol-OD >99.5 Atom % D
- 2-Methyl-2-propan(ol-d), tert-Butanol-OD, tert-Butyl alcohol-d
- TERT-BUTANOL-O-D, 98+ ATOM % D, FOR NMR
- 1,1-Dimethyl(O-2H)ethanol
- 2-[(2H)Hydroxy]-2-methylpropane
- 2-Methyl-(O-2H)-2-propanol
- CAS:
- 3972-25-6
- MF:
- C4H9DO
- MW:
- 75.13
- EINECS:
- 223-597-1
- Mol File:
- 3972-25-6.mol
2-METHYL-2-PROPAN(OL-D) Chemical Properties
- Melting point:
- 23-26 °C (lit.)
- Boiling point:
- 83 °C (lit.)
- Density
- 0.786 g/mL at 25 °C
- refractive index
- n20/D 1.3847(lit.)
- Flash point:
- 52 °F
- storage temp.
- Flammables area
- solubility
- Acetone, Chloroform (Slightly), Methanol (Slightly)
- form
- Solid
- color
- Colourless Oil to White
- explosive limit
- 2.3-8.0%(V)
- InChI
- 1S/C4H10O/c1-4(2,3)5/h5H,1-3H3/i5D
- InChIKey
- DKGAVHZHDRPRBM-UICOGKGYSA-N
- SMILES
- [2H]OC(C)(C)C
- CAS Number Unlabeled
- 75-65-0
Safety Information
- Hazard Codes
- F,Xn
- Risk Statements
- 11-20-36/37
- Safety Statements
- 9-16-46
- RIDADR
- UN 1120 3/PG 2
- WGK Germany
- 3
- Storage Class
- 3 - Flammable liquids
- Hazard Classifications
- Acute Tox. 4 Inhalation
Eye Irrit. 2
Flam. Liq. 2
STOT SE 3
MSDS
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
2-METHYL-2-PROPAN(OL-D) Usage And Synthesis
Chemical Properties
clear colorless liquid
Uses
Labelled Tert-butyl Alcohol is used as an organic solvent. Also it is used in the synthesis of proteosome inhibitors that are quite potent.
Uses
Tert-butyl Alcohol-OD is used as an organic solvent. Also it is used in the synthesis of proteosome inhibitors that are quite potent.
Synthesis
Deuterated tert-butanol can be used in organic synthesis, such as the preparation of ??,??-dideuterated alcohols, and an example of its application is as follows: in a 10 mL single-necked flask protected by nitrogen, 95.1 mg (0.50 mmol) of Compound 1d was added, 2.5 mL of tetrahydrofuran, 187.8 mg (2.50 mmol) of deuterated tert-butanol (t-BuOD), a 51.7 mg (2.25 mmol) sodium block, stirred for 5 min at 0 ??C. Raise to room temperature and burst the reaction with 3.0 M aqueous hydrochloric acid. Extracted by adding ether with saturated saline, the organic phase was dried, concentrated and separated by column chromatography to give 37.3 mg of the target compound in 54% yield.
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