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Trimethyl orthoformate

Catalog No. A13760 Name Alfa Aesar
CAS Number 149-73-5 Website
M. F. C4H10O3 Telephone
M. W. 106.1204 Fax
Purity 99% Email
Storage Chembase ID: 104754

SYNONYMS

Title
原甲酸三甲酯
IUPAC name
trimethoxymethane
IUPAC Traditional name
trimethyl orthoformate
Synonyms
Orthoformic acid trimethyl ester
Methyl orthoformate

DATABASE IDS

Beilstein Number 969215
Merck Index 146884
MDL Number MFCD00008483
EC Number 205-745-7
CAS Number 149-73-5

PROPERTIES

Purity 99%
Boiling Point 101-102°C
Density 0.968
Flash Point 15°C(59°F)
Melting Point -53°C
Refractive Index 1.3790
GHS Pictograms GHS02
GHS Pictograms GHS07
GHS Hazard statements H225-H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
European Hazard Symbols Flammable Flammable (F)
GHS Precautionary statements P210-P241-P303+P361+P353-P305+P351+P338-P405-P501A
Risk Statements 11-36/37/38
RTECS RM6650000
Safety Statements 26-37-60
Storage Warning Moisture Sensitive
TSCA Listed
Hazard Class 3
UN Number UN3272
Packing Group II

DETAILS

REFERENCES

  • For further reactions of alkyl orthoformates, see Triethyl orthoformate, A13587.
  • Protects the cis-2,3-diol system of ribonucleosides as their methoxymethylene acetals (cyclic orthoformates), readily hydrolyzed by mild acid: Synthesis, 408 (1985).
  • In the presence of HCl, is an alternative to formic acid in the synthesis of benzoxazoles from ortho-amino phenols: Org. Prep. Proced. Int., 22, 613 (1990).
  • Reagent for the acid-catalyzed conversion of ketones to their methyl enol ethers in good yield: Synthesis, 38 (1974). For an example, see: Org. Synth. Coll., 8, 357 (1993).