| Identification | More | [Name]
BREDERECK'S REAGENT | [CAS]
5815-08-7 | [Synonyms]
BREDERECKS REAGENT
BREDERECK'S REAGENT
BUTOXYBIS(DIMETHYLAMINO)METHANE
T-BUTOXYBIS(DIMETHYLAMINO)METHANE
TERT-BUTOXYBIS(DIMETHYLAMINO)METHANE
tert-Butoxybis(dimethylamino)methane, 85+%
Methanediamine, 1-(1,1-dimethylethoxy)-N,N,N,N-tetramethyl-
TERT-BUTOXY BIS(DIMETHYLAMINO)METHANE (BREDERECKS REAGENT)
tert-Butoxybis(dimethylamino)methane, tech.
Bis(dimethylamino)(tert-butoxy)methane
N,N,N',N'-Tetramethyl(tert-butoxy)methanediamine
N,N,N',N'-Tetramethyl-α-tert-butoxymethanediamine
α-(1,1-Dimethylethoxy)-N,N,N',N'-tetramethylmethanediamine
α-tert-Butoxy-N,N,N',N'-tetramethylmethanediamine | [EINECS(EC#)]
227-383-9 | [Molecular Formula]
C9H22N2O | [MDL Number]
MFCD00042858 | [Molecular Weight]
174.28 | [MOL File]
5815-08-7.mol |
| Chemical Properties | Back Directory | [Appearance]
Clear pale yellow liquid | [Boiling point ]
50-55 °C/15 mmHg (lit.) | [density ]
0.844 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.422(lit.)
| [Fp ]
106 °F
| [storage temp. ]
Freezer (-20°C) | [form ]
Liquid | [pka]
5.46±0.38(Predicted) | [color ]
Clear pale yellow | [Specific Gravity]
0.844 | [BRN ]
1901973 | [InChIKey]
HXRAMSFGUAOAJR-UHFFFAOYSA-N | [CAS DataBase Reference]
5815-08-7(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi,F | [Risk Statements ]
R10:Flammable.
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [RIDADR ]
UN 1993 3/PG 3
| [WGK Germany ]
3
| [F ]
10 | [HazardClass ]
3 | [PackingGroup ]
III | [HS Code ]
29221990 |
| Hazard Information | Back Directory | [Chemical Properties]
Clear pale yellow liquid | [Uses]
Mild enamination reagent; catalyst in ring-opening polymerization reactions. | [Uses]
Reactant for:• ;Preparation of pyrroloquinazolines as photochemotherapeutic agents1• ;Enanatioslective formal synthesis of the Cinchona alkaloid quinine via stereoselective intermolecular radical addition2• ;Synthesis of camptothecin via intramolecular isomuenchnone cycloaddition reaction3• ;Aminomethylenation reactions4 |
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