METHYL (TRIMETHYLSILYL)ACETATE
METHYL (TRIMETHYLSILYL)ACETATE
  • CAS No.:2916-76-9
Other grades of this product :
METHYL (TRIMETHYLSILYL)ACETATE Basic information
Product Name:METHYL (TRIMETHYLSILYL)ACETATE
Synonyms:METHYLTRIMETHYLSILICATE;METHYL (TRIMETHYLSILYL)ACETATE;Methyl 2-(triMethylsilyl)acetate;2-(Trimethylsilyl)acetic acid methyl ester;2-[Dimethyl(methyl)silyl]acetic acid methyl ester;Trimethylsilylacetic acid methyl ester;Methyl (trimethylsilyl)acetate,98%;Acetic acid, 2-(trimethylsilyl)-, methyl ester
CAS:2916-76-9
MF:C6H14O2Si
MW:146.26
EINECS:220-845-0
Product Categories:C6 to C7;Carbonyl Compounds;Esters
Mol File:2916-76-9.mol
METHYL (TRIMETHYLSILYL)ACETATE Chemical Properties
Boiling point 38-39 °C13 mm Hg(lit.)
density 0.891 g/mL at 25 °C(lit.)
refractive index n20/D 1.414(lit.)
Fp 91 °F
storage temp. Flammables area
Specific Gravity0.890
Hydrolytic Sensitivity2: reacts with aqueous acid
BRN 1098961
Safety Information
Hazard Codes F,Xi
Risk Statements 11-36/37/38
Safety Statements 16-26-36
RIDADR UN 3272 3/PG 3
WGK Germany 3
10-21
TSCA No
HazardClass 3.1
PackingGroup II
HS Code 29319090
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
METHYL (TRIMETHYLSILYL)ACETATE Usage And Synthesis
Chemical PropertiesCLEAR COLOURLESS LIQUID
UsesMethyl 2-(Trimethylsilyl)acetate is a useful compound in the organic synthesis.
General DescriptionMethyl trimethylsilylacetate on reaction with lithium diisopropylamide in THF at -78°C yields methyl lithiotrimethylsilylacetate. It also undergoes Peterson olefination to yield mainly Z-isomers of steroid 17β-side chain methyl acrylates.
Purification MethodsMethyl trimethylsilylacetate [2916-76-9] M 146.3, b 65-68o/50mm, d 4 0.89. Dissolve it in Et2O, shaken with 1M HCl, wash with H2O, aqueous saturated NaHCO3, H2O again, and dry it (a precipitate may be formed in the NaHCO3 solution and should be drawn off and discarded). The solvent is distilled off, and the residue is fractionated through a good column. IR (CHCl3) max 1728cm1 . [Fessenden & Fessenden J Org Chem 32 3535 1967, Matsuda et al. J Org Chem 45 237 1980, Beilstein 4 III 1855, 4 IV 3974 for Et ester.]
METHYL (TRIMETHYLSILYL)ACETATE Preparation Products And Raw materials
Preparation Products(3-NITROPHENYL)ACETIC ACID METHYL ESTER-->METHYL TRANS-2-HEXENOATE, 98

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