1,1-Di-tert-butoxytrimethylamine

1,1-Di-tert-butoxytrimethylamine Basic information
Product Name:1,1-Di-tert-butoxytrimethylamine
Synonyms:N,N-DIMETHYLFORMAMIDE DI-TERT-BUTYL ACET AL, DERIVATIZATION GRADE;1,1-Di-tert-butoxytrimethylamine, 1,1-Di-tert-butoxy-N,N-dimethylmethylamine;N,N-Dimethyl-1,1-bis[(2-methylpropan-2-yl)oxy]methanamine;Di-tert-butoxy(dimethylamino)methane;N,N-Dimethyldi(tert-butyloxy)methanamine;N,N-Dimethyldi-tert-butoxymethanamine;N,N-Dimethylformamide di-tert-butyl acetal, tech. 90%;N,N-Dimethylformamide Di-tert-butyl Acetal [for Esterification]
CAS:36805-97-7
MF:C11H25NO2
MW:203.32
EINECS:253-222-7
Product Categories:Analytical Chemistry;Esterification & Alkylation (GC Derivatizing Reagents);GC Derivatizing Reagents;N,N-Dimethylformamide Dialkylacetals (GC Derivatizing Reagents)
Mol File:36805-97-7.mol
1,1-Di-tert-butoxytrimethylamine Structure
1,1-Di-tert-butoxytrimethylamine Chemical Properties
Boiling point 56-57 °C8 mm Hg(lit.)
density 0.848 g/mL at 25 °C(lit.)
refractive index n20/D 1.413(lit.)
Fp 93 °F
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility Miscible with toluene and benzene.
pka5.34±0.50(Predicted)
form clear liquid
color Colorless to Almost colorless
Specific Gravity0.848
Sensitive Moisture Sensitive
BRN 969629
InChIKeyDBNQIOANXZVWIP-UHFFFAOYSA-N
CAS DataBase Reference36805-97-7(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 10-36/37/38
Safety Statements 26-36
RIDADR UN 1993 3/PG 3
WGK Germany 3
10-21
HazardClass 3
PackingGroup III
HS Code 29221990
MSDS Information
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1,1-Di-tert-butoxy-N,N-dimethylmethylamine English
SigmaAldrich English
ALFA English
1,1-Di-tert-butoxytrimethylamine Usage And Synthesis
UsesN,N-Dimethylformamide di-tert-butyl acetal may be used in the synthesis of following:
  • (S)-2-(1-tert-butoxycarbonyl-2-{4-[2-(5-methyl-2-phenyloxazol-4-yl)ethoxy]phenyl}ethylamino)benzoic acid methyl ester
  • 3-O-tert-butylmorphine
  • tert-butylesters of pyrrole- and indolecarboxylic acids
UsesReagent used for the preparation of indolizines via intermolecular cyclization of picolinium salts.
Synthesis Reference(s)Synthetic Communications, 15, p. 723, 1985 DOI: 10.1080/00397918508063864
General DescriptionN,N-Dimethylformamide di-tert-butyl acetal is an derivatizing reagent.
1,1-Di-tert-butoxytrimethylamine Preparation Products And Raw materials
Preparation Productst-butyl 6-bromo-3-pyridinecarboxylate-->Ne-Boc-L-lysine tert-butyl ester hydrochloride-->3-Pyridinecarboxylic acid, 6-fluoro-, 1,1-diMethylethyl ester-->tert-butyl 3-bromo-4-methylbenzoate-->5,6-Dichloro-nicotinic acid tert-butyl ester-->OCTADECANEDIOIC ACID MONO-TERT-BUTYL ESTER
N,N-Dimethylformamide dimethyl acetal 4-Chlorophenol 1,1-Diisopropoxytrimethylamine N,N-Dimethylformamide Recombinant Human Telomerase Buprofezin 1,1-Di-tert-butoxytrimethylamine 1-TERT-BUTOXY-1-METHOXY-TRIMETHYLAMINE Acetal Trimethylamine N,N-Dimethyformamide diethy acetal Butyl acetate PHENYLETHYL ACETAL Polyoxymethylene DI-TERT-BUTYL ETHER 2-Butoxyethanol

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